Laryngeal and Hypopharyngeal Cancer

What Are Laryngeal and Hypopharyngeal Cancers?

Laryngeal cancer affects the larynx (lair-inks) which is often called the "voice box" or the "Adam's apple." As shown in the picture below, the larynx has 3 main sections:

  • the glottis (vocal cords)
  • the supraglottis (area above the vocal cords, including the epiglottis, which closes off when you swallow food)
  • the subglottis (the area below the vocal cords)

Cancers that start in different parts of the larynx are treated differently.

The larynx and vocal cords sit above the trachea and are the entrance to the lungs. The larynx makes sound for speaking and protects the airway during swallowing. The vocal cords change the sound and pitch of the vice. They close tightly when a person swallows and open to allow breathing.

Cancer can also affect the hypopharynx which surrounds the larynx. It part of the esophagus or food pipe. Food enters the esophagus here as it passes through the neck and chest into the stomach.

Cancers of the larynx and hypopharynx are both covered here because they are so close to each other. Several types of cancer form in these 2 areas.

Almost all of these cancers start from the thin, flat cells (squamous cells) that line the larynx and hypopharynx. Squamous cell cancer does not form suddenly. It starts when the cells begin to change. Smoking and heavy alcohol drinking usually cause the changes. The cells become pre-cancers. Most pre-cancers will not become cancers. If the causes (like smoking) stop, these pre-cancers usually go away.

But some pre-cancers do grow into cancers. The earliest form of cancer is called carcinoma in situ (in si-too) or CIS. This is where only the cells of the lining layer are affected. In situ is a Latin term that means "in place." CIS has not yet spread into lower layers of cells or spread to other parts of the body. Some of these very early cancers go away on their own. Most can be cured by stripping or cutting away the lining layer of cells, or by destroying them with a laser beam. If CIS is not treated it can develop into cancer that can spread into nearby tissue and to other parts of the body.

While other kinds of cancer can start in the glands and tissue of the larynx and hypopharynx, they are very rare. The information here refers only to squamous cell cancer.

What Causes Laryngeal and Hypopharyngeal Cancers?

A risk factor is anything that affects your chance of getting a disease such as cancer. Different cancers have different risk factors. Some risk factors, such as smoking, can be controlled. Others, like a person's age or race, can't be changed. But having a risk factor, or even several, does not mean that you will get the disease. And many people who do get the disease did not have any known risk factors.

Risk Factors for These Cancers

Tobacco Use

Most people who get these cancers are smokers. The risk is many times greater in smokers than in those who don't smoke. The more a person smokes, the greater the risk. Even chewing tobacco has been reported to raise the risk of these cancers.

Alcohol Abuse

Heavy drinkers have a much greater risk of cancer of the larynx. Using both tobacco and alcohol greatly increases the risk.

Diet

Poor eating habits often go along with alcohol abuse. This may be why alcohol abuse raises the risk of these cancers. A lack of foods with B vitamins and vitamin A may also play a role.

HPV

HPV stands for human papilloma virus. Most of these viruses cause warts on the hands, feet, and other places. Some also cause cancers of the sex organs. HPV may be a factor in some cases of cancer of the larynx and hypopharynx as well.

Weak Immune System

These cancers are more common in people who have a weak immune system. This can be caused by diseases present at birth, by AIDS, or by certain drugs that people who have had organ transplants need to take.

Work Hazards

Long and intense exposure to wood dust, paint fumes, and to certain chemicals can increase the risk of these cancers. Working with asbestos, used in the past as insulation, may also increase laryngeal cancer risk.

Gender

These cancers are between 4 and 5 times more common in men than in women. In the past, men were more likely to smoke and drink. But now this is changing and women's risks are increasing.

Age

Because these cancers take a long time to grow, they are not common in young people. Most people are over 65 when these cancers are first found.

Race

These cancers are more common among African Americans than among whites.

Heartburn

This disease, called GERD (gastroesophageal reflux disease) by doctors, might be a risk factor for these cancers.

How Are Laryngeal and Hypopharyngeal Cancers Found?

Many cancers of the larynx and some of the hypopharynx can be found early. Cancer that forms on the vocal cords are often found at an early stage because they cause hoarseness. Cancers that start above or below the vocal cords are often found at later stages. Talk to your doctor if you have any of these symptoms:

  • sore throat that doesn't go away
  • constant coughing
  • trouble swallowing or pain with swallowing
  • ear pain that doesn't go away
  • trouble breathing
  • weight loss
  • hoarseness that lasts more than 2 weeks
  • lump or mass in the neck

Tests to Find Out if You Have Laryngeal or Hypopharyngeal Cancer

History and Physical Exam

If there is any reason to suspect cancer, the first step is for the doctor to gather facts about your symptoms, risk factors, family history and medical conditions. You will have a physical exam and your doctor will ask you questions about your health. Your doctor will probably refer you to a doctor with special training in these cancers (an otolaryngologist). You will also need to have some tests. These might include any of the following:

Blood tests

Blood tests won't tell if you have these cancers, but they will provide information about your overall health.

Complete Head and Neck Exam

If there is reason to suspect a cancer, you will be sent to a head and neck surgeon. The larynx and hypopharynx are deep inside the neck and not easy to check. This doctor will give you an exam with a mirrors and special fiber-optic scope. This flexible, lighted tube will be put through the mouth or nose. The scope helps the doctor to "see" these areas. The mouth, neck, and nose will be carefully checked, too.

Panendoscopy (Pan-en-dos-kuh-pee)

If the doctor suspects you have cancer in the head and neck he or she will do a complete exam of this area. This exam is done in the operating room while the patient is asleep (under general anesthesia.) The surgeon looks at the entire area through a scope and may take a sample of tissue (biopsy) to be looked at under a microscope. Biopsy is discussed below.

Once a tumor has been found, imaging studies may be useful in finding out how far it has spread.

Imaging Tests

CT or CAT Scan (Computed Tomography)

These scans use x-rays to take a series of pictures of the body from many angles. A computer combines the pictures to form a detailed image. This test can help your doctor learn the size of the tumor and whether it has spread to the lymph nodes or nearby tissue. CT scans take longer than standard x-rays. You will need to lie still on a table while they are being done. You may also have an IV (intravenous) line through which a contrast "dye" is injected.

MRI (Magnetic Resonance Imaging)

Like a CT scan, an MRI displays a cross-sectional picture of the body. But the MRI uses radio waves and strong magnets instead of x-rays. MRI scans take longer than CT scans--often up to an hour. Also, you are placed in a narrow tube which can upset some people. Newer, "open" MRI machines can help with this if needed. A contrast dye might be injected just as with CT scans.

Barium Swallow

This is a series of x-rays taken while you swallow a liquid with barium in it. Barium coats the inside surface of the throat and helps create a good picture.

Chest X-ray

This is routine for people with head and neck cancers. It is done to check for lung cancer and emphysema.

PET Scan

PET scans use a form of sugar that contains a radioactive atom. Most cancer cells in the body absorb large amounts of this sugar. A special camera can find where the sugar has collected. Your doctor can use this test to see if the cancer has spread to lymph nodes or other places. Newer machines combine CT and PET scans to even better pinpoint the tumor.

Biopsy

A biopsy is a test that involves taking a sample of tissue to see if it contains cancer cells. It is the only sure way to know that a growth is cancer. There are many different types of biopsies that might be done to check for cancer cells. Some are done in the operating room with the patient asleep. Others can be done with a thin (fine) needle in the doctor's office.

How Are Laryngeal and Hypopharyngeal Cancer Treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.

The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.

Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.

There is a lot for you to think about when choosing the best way to treat or manage your cancer. Often there is more than one treatment to choose from. Take time to think about all of the choices. Two things to consider are the type of cancer and the stage (extent) of the cancer. But your age, your overall health, and your own preferences are also important.

It's often a good idea to get a second opinion, perhaps from a doctor who has treated this type of cancer. A second opinion can give you more information and help you feel better about the treatment plan you choose.

The Main Types of Cancer Treatment

The 3 main types of treatments for these cancers are:

  • surgery
  • radiation
  • chemotherapy

Sometimes 2 or more of these treatments are used together. If it doesn't look like the cancer can be cured, the goal of treatment might be to remove or destroy as much of the cancer as possible to delay the spread or return of the cancer. Sometimes treatment is aimed at relieving symptoms. This is called palliative treatment.

If at all possible, the doctor will try to save your larynx and voice. Most experts do not recommend removing the larynx unless there are no other options. People who lose their voice can suffer from feeling depressed and lonely.

Surgery

There are several kinds of surgery for these cancers. Some may remove the cancer. Others help restore the look and function of the head and neck.

Vocal Cord Stripping

This method involves using a long tool to strip away the cancer in the top layers of tissue of the vocal cords. Very early (stage 0) cancers are sometimes treated this way.

Cordectomy

This method involves removing all or part of the vocal cords..

Laser Surgery

Lasers can be used to treat some early cancers. An endoscope is used to find the tumor which is then "zapped� or cut out with a laser.

Partial Laryngectomy (lair-in-jek-tuh-me)

Smaller cancers of the larynx can often be removed without taking out the entire voice box. The goal is to leave as much of the voice box as possible while removing the cancer. Sometimes it is even possible to preserve some speech.

Total Laryngectomy

This surgery involves taking out the entire voice box. The windpipe must be brought up to the front of the neck as a hole (stoma). The person then breathes through this stoma.

Possible complications after this surgery include bleeding, development of a fistula (an abnormal opening), development of a stricture (narrowing), and having food or liquid enter the lungs (aspiration). Aspiration can lead to pneumonia.

Before and After Surgery

Illustrations by permission of the Mayo Foundation. From "Looking Forward...A Guidebook for the Laryngectomee" by R.L. Keith, et al, New York, Thieme-Stratton, Inc. and copyrighted by the Mayo Foundation, 1984.

Total or Partial Pharyngectomy (fair-in-jek-tuh-me)

This operation is done for cancers of the hypopharynx. All or part of the hypopharynx is removed. Surgery may also be done to rebuild the throat. This will help the patient to swallow after the operation. Most often, the larynx will also be removed.

Flap Methods

Sometimes a muscle and area of skin may be moved from an area close to your throat, such as the chest, to rebuild the throat after surgery. Tissues from other parts of your body such as a piece of intestine or a piece of arm muscle may also be used to replace parts of your throat.

Neck Dissection

Because these cancers often spread to the lymph nodes in the neck, it may be necessary to remove these lymph nodes. This is called a "neck dissection." The amount of tissue to be removed depends on the size of the cancer and how much it has spread.

Tracheotomy

If a tumor is too large to remove or is blocking the windpipe, an opening may be made in the neck. This will bypass the tumor and help with breathing.

Gastrostomy Tube (G-tube or feeding tube)

Surgery may also be done to improve nutrition. A patient who cannot swallow enough food may need a feeding tube placed through the skin in the belly (abdomen) directly into the stomach.

Effect of Surgery on Speech

This can vary. If the surgery does not damage the vocal cords, then speech may be normal. With any more extensive surgery, there will usually be hoarseness. Any larger operation, especially laryngectomy, will eliminate normal speech altogether. (See the section "Restoring Speech After Total Laryngectomy.")

Radiation Therapy

Radiation therapy is treatment with high energy rays (such as x-rays) to kill or shrink cancer cells. The radiation may come from outside the body (external radiation) or from radioactive materials placed directly in the tumor. External radiation is often the main treatment for laryngeal and hypopharyngeal cancer. It may be used instead of surgery for small cancers that can be destroyed without surgery. It is also used for patients whose health does not permit them to have surgery. Often chemotherapy is also given.

Treatment is usually given daily, 5 days per week, for about 7 weeks. Other schedules for treatment are being studied.

Radiation can also be used after surgery to kill cancer cells that could not be seen during surgery. Radiation can be used to ease symptoms such as pain, bleeding, and problems with swallowing, too. It can be used to ease problems caused by cancer that has spread to bones. Side effects from radiation could include the following:

  • mild skin problems
  • dry mouth (which can lead to problems with tooth decay)
  • sore throat
  • hoarseness
  • trouble swallowing
  • decreased sense of taste
  • problems with breathing from swelling of the larynx
  • tiredness

Most of these side effects go away after a short while. Talk to your doctor or nurse if you are having trouble with any side effects. There are often ways to help.

Chemotherapy

Chemotherapy or chemo refers to the use of drugs to kill cancer cells. Usually the drugs are given into a vein or by mouth. Once the drugs enter the bloodstream, they spread throughout the body.

Chemo is useful in treating cancer that has spread to organs beyond the head and neck. It has also been used to ease symptoms of tumors that are too large to be completely removed and that radiation treatment has not been able to control. Many doctors now recommend chemo along with radiation as the main treatment for large larynx cancer instead of laryngectomy (see below).

Chemo can have some side effects. These side effects will depend on the type of drugs given, the amount taken, and how long treatment lasts. Side effects could include the following:

  • nausea and vomiting
  • loss of appetite
  • hair loss
  • mouth sores
  • a higher chance of infection (from a shortage of white blood cells)
  • bleeding or bruising after minor cuts or injuries (caused by a shortage of blood platelets)
  • shortness of breath
  • tiredness (from low red blood cell counts)

Most side effects go away after treatment ends. Anyone who has problems with side effects should talk with their doctor or nurse, as there are often ways to help.

Chemo with Radiation Therapy (Chemoradiotherapy)

Chemo given at the same time as radiation can shrink tumors better than either treatment alone. Studies are going on to find out whether this combination can control advanced disease that is confined to the head and neck area. This treatment may help people avoid large operations that cause loss of natural speech.

Survival Rates by Stage for These Cancers

Below are listed the 5-year relative survival rates for cancers from each of the sites. The 5-year survival rate refers to the percentage of patients who live at least 5 years after their cancer is found. Keep in mind that many of these patients live much longer than 5 years after diagnosis.

While these numbers give an overall picture, every person is different. Statistics can't predict what will happen in your case. Talk with your cancer care team if you have questions about your own chances of a cure, or how long you might survive your cancer. They know your situation best.


Supraglottis

Stage 5-year relative survival
I 83%
II 70%
III 57%
IV 43%

Glottis

Stage
5-year relative survival
I
65%
II
62%
III
55%
IV
37%

Subglottis (These numbers are less accurate because of the small number of patients.)

Stage
5-year relative survival
I
54%
II
68%
III
53%
IV
36%

Hypopharynx

Stage
5-year relative survival
I
41%
II
36%
III
36%
IV
20%

Kidney Cancer

What Is Kidney Cancer?

Kidney cancer is also called renal carcinoma. It is a cancer that starts in the kidneys. In order to understand kidney cancer, it helps to know how the normal kidneys look and work..

About the Kidneys

The kidneys are about the size of your fist. These two bean-shaped organs are shown in the picture below. One is just to the left and the other to the right of the backbone. The lower rib cage protects the kidneys.

The kidneys' main job is to filter the blood and help the body get rid of excess water, salt, and waste products in the form of urine. Urine travels through long, thin tubes (called ureters) to the bladder where it is stored until the person passes the urine, or urinates.

Although we have two kidneys, it is possible to survive with less than even one complete kidney. Some people live without any working kidneys at all. Their blood is filtered by a machine in a process called dialysis.

Kidney Cancer (Renal Cell Carcinoma--RCC)

The most common type of kidney cancer is called renal cell cancer. It accounts for more than 9 out of 10 cases of kidney cancer. While there are other types of kidney tumors, the information that follows refers only to renal cell cancer. The American Cancer Society has more information about other types of kidney tumors available through our toll-free number or on our Web site.

Like all cancers, kidney cancer begins small and grows larger over time. It usually grows as a single mass within the kidney. But a kidney can have more than one tumor. Sometimes tumors are found in both kidneys at the same time. The cancer might be found only after it has become very large. Most of the time it is found before it has spread to other organs through the bloodstream. This is good because like most cancers, kidney cancer can be hard to treat after it has spread (metastasized).

Types of Kidney Cancer

There are several subtypes of RCC, based mainly on how the cancer cells look under a microscope:

Clear Cell RCC

This is the most common form of renal cell carcinoma. About 8 out of 10 people with RCC have this kind of cancer. When seen under a microscope, the cells that make up clear cell RCC look very pale or clear.

Papillary RCC

This is the second most common subtype -- about 10% to 15% of people have this kind. These cancers form little finger-like projections (called papillae) in some, if not most, of the tumor. Some doctors call these cancers chromophilic because the cells take up certain dyes used to prepare the tissue to be looked at under the microscope. The dyes make them look pink.

Chromophobe RCC

This subtype accounts for about 5% of RCCs. The cells of these cancers are also pale, like the clear cells, but are much larger and differ in other ways, too.

Collecting Duct RCC

This subtype is very rare. The major feature is that the cancer cells can form irregular tubes.

Unclassified RCC

In rare cases, renal cell cancers are labeled as "unclassified" because they don't fit into any of the other categories or because more than one type of cell is present.

How Is Kidney Cancer Found?

Many kidney cancers are found fairly early, while they are still confined to the kidney. But others are found at a more advanced stage. There are a few reasons why kidney cancer may not be found until later:
  • The cancer may become quite large without causing any pain or other problems.
  • Because the kidneys are deep inside the body, small kidney tumors cannot be seen or felt during a physical exam.
  • There are no simple tests that can be used to look for kidney cancer in people who are not at increased risk.

Small amounts of blood in the urine could point to kidney cancer, but there are many other causes of blood in the urine, including infections and kidney stones. And some people with kidney cancer don�t have blood in their urine until the cancer is quite large.

While tests such as CT scans (computed tomography) and MRI (magnetic resonance imaging) can sometimes find small tumors, these tests are expensive and can�t always tell cancerous tumors from benign ones. They are recommended routinely only for a very few people with certain risk factors.

It is important to tell your doctor if members of your family have had kidney cancer or other problems linked to kidney disease.

Often kidney cancer is found "incidentally," meaning that the cancer is found during tests for some other illness such as gallbladder disease. The survival rate for kidney cancer found this way is very high because the cancer is usually found at a very early stage.

Signs and Symptoms of Kidney Cancer

While early kidney cancers do not usually cause any signs or symptoms, larger ones may. Possible signs and symptoms of kidney cancer include:

  • blood in the urine
  • low back pain on one side (not from an injury)
  • a mass or lump on the side or lower back
  • tiredness
  • weight loss, if you are not trying to lose weight
  • fever that doesn�t go away after a few weeks and that is not from a cold, the flu, or other infection
  • swelling of ankles and legs

Talk to your doctor if you notice any of these problems. They are often caused by less serious conditions, but only your doctor can tell for sure. If there is any reason to suspect kidney cancer, the doctor will take your medical history and do a physical exam. Then one or more tests may be done.

Imaging Tests

Imaging tests are used to create pictures of the inside of your body. These tests may be done for a number of reasons:

  • to help find out whether a certain area might be cancerous
  • to learn how far cancer may have spread
  • to help see whether treatment is working

In many cases, imaging tests are able to be show whether a mass in the kidney is cancer or not, but in some cases a biopsy may be needed to be sure.

CT Scan (Computed Tomography)

A CT (or CAT scan) is a special type of x-ray in which several pictures are taken from different angles and then combined by a computer to give a detailed image of the inside of the body. Often after the first set of pictures is taken you will get an injection of a contrast �dye� that helps to outline structures in your body. Then a second set of pictures is taken. The dye may cause some flushing (a feeling of warmth, especially in the face). Some people are allergic and get hives. Rarely, more serious reactions like trouble breathing or low blood pressure can happen. Be sure to tell the doctor if you have ever had a reaction to any contrast material used for x-rays. CT scans take longer than normal x-rays, but they are getting faster all the time.

A CT scan is one of the most useful tests for finding and looking at a tumor inside your kidney. It is also useful in checking whether or not a cancer has spread to organs and tissues beyond the kidney. The CT scan will give precise information about the size, shape, and place of a tumor, and can help find enlarged lymph nodes that might contain cancer.

MRI (Magnetic Resonance Imaging)

MRI scans use strong magnets and radio waves instead of x-rays to take pictures. MRI scans take longer than x-rays�often up to an hour. Also, you have to be placed inside a tube-like machine, which upsets some people. Newer, "open" MRI machines can sometimes help with this if needed. An MRI gives more detailed pictures than a CT scan. MRI scans are used less often than CT scans in people with kidney cancer.

Ultrasound

Ultrasound uses sound waves to create images of internal organs. A wand (transducer) is moved over the skin; it gives off sound waves and picks up the echoes as they bounce back. This test is painless and easy to take. Ultrasound can be helpful in finding out whether a kidney mass is solid or filled with fluid. If a kidney biopsy is needed, this test can be used to guide a needle into the mass to take a sample.

PET Scan (Positron Emission Tomography)

PET scans involve injecting a slightly radioactive form of sugar into the bloodstream. The substance travels throughout the body. Cancer cells absorb large amounts of the sugar and a special camera is then used to find these deposits and turn them into pictures. This test is useful to see if the cancer has spread to lymph nodes. PET scans can also be used when the doctor thinks the cancer has spread but doesn�t know where. Some newer machines are able to do both a PET and CT scan at the same time.

Intravenous Pyelogram (IVP)

An IVP is an x-ray of the kidney taken after a special dye is injected into a vein. This dye travels from the blood into the kidneys and then passes into the ureters and bladder. X-rays taken can help find a cancer or show any damage caused by the tumor. You might not need an IVP if you have already had a CT or MRI.

Angiography

Like the IVP, this x-ray test also uses a contrast dye. but the dye is injected into an artery leading to the kidney. It can help outline the blood vessels feeding a kidney tumor which in turn helps doctors plan surgery to remove the tumor.

Chest X-Ray

A chest x-ray can show if the cancer has spread to the lungs. This is very unlikely unless the cancer is very advanced. If the results are normal, you probably don't have cancer in your lungs.

Bone Scan

A bone scan can help show if a cancer has spread to your bones. A slightly radioactive substance is injected into a vein. It travels to the bones, where it can be seen by a special camera. By itself, a bone scan can't show the difference between cancer and problems such as arthritis, so other tests may be needed.

Lab Tests

Lab tests may be done to get a sense of a person's overall health and to help tell if cancer has spread to other areas. Before surgery, they can help tell if a person is healthy enough to have an operation.

Urinalysis

This is likely to be one of the first tests done if kidney cancer is a possibility. Urine tests looks for blood and other substances in a urine sample. Sometimes special microscopic tests (called urine cytology) will be done to look for cancer cells.

Blood Tests

Blood tests are done to look for problems that might occur along with kidney cancer, such as too few or too many red blood cells.

FNA Biopsy (Fine Needle Aspiration)

This test may be done if other tests have not shown for sure that there is a cancer. During FNA, a thin needle is placed through the skin and guided by CT or ultrasound into the area of concern. Then fluid or small pieces of tissue are removed (from the kidney or from another place where the cancer may have spread). The sample is looked at under a microscope to see if it contains cancer cells.

How Is Kidney Cancer Treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.

The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.

Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.

After the cancer is found and staged, your doctor will talk with you about different treatment plans. It is important to take time and think about your choices. One of the most important factors is the stage of the cancer. Other things to take into account include your overall health, the likely side effects of the treatment, and the chances of curing the disease, helping you live longer, or relieving symptoms.

If you have kidney cancer, your treatment options may include surgery, radiation therapy, targeted therapy, immunotherapy, chemotherapy, or some combination of these. You might want to get a second opinion. This may give you with more information and help you feel more confident about the treatment plan you have chosen.

Surgery

Surgery is the main treatment for renal cell cancer. The chances of surviving kidney cancer without having surgery are small. Depending on the type and stage, you might have one of the following:

Radical Nephrectomy

In this operation, the whole kidney, the adrenal gland (the gland that �sits� on top of the kidney), and some nearby fatty tissue are removed. Nearby lymph nodes are sometimes removed too (regional lymphadenectomy). Most people do fine with only one kidney.

"Keyhole" Surgery

The medical term for this approach is laparoscopic nephrectomy. In this method for removing kidney tumors, the operation is done through small incisions. Through these incisions, the surgeon can use instruments to do the surgery. The advantages include a shorter hospital stay, faster recovery, and less pain afterwards.

Removing Lymph Nodes (Lymph Node Dissection)

This method involves removing nearby lymph nodes to see if they contain cancer. Many doctors do this along with the radical nephrectomy. The main reason for doing it is to see for sure whether the cancer has reached the lymph nodes, instead of relying only on imaging study results. This information can be important in choosing among treatment options.

Partial Nephrectomy

This is also called nephron-sparing surgery. The surgeon removes only the part of the kidney with the cancer. The rest of the organ is left in place. This might be a choice if your cancer is in both kidneys, if you have only one kidney, or if there is a very small cancer in only one kidney.

Removal of Metastases

Sometimes surgery is done to remove cancer that has spread. This can help relieve pain or other symptoms even though it does not usually help patients live longer. It is most often done if there are only a few tumors that can be removed easily.

Risks of Surgery

Surgery always involves some risks. The following are some possible risks of surgery for kidney cancer:

  • bleeding during surgery or after surgery that may require blood transfusions
  • wound infection
  • damage to internal organs and blood vessels during surgery
  • unwanted air in the chest cavity
  • bulging (hernia) of internal organs near the incision
  • failure of the remaining kidney

Other Types of Treatments

While surgery is the main treatment for kidney cancers that can be removed, some people are too sick to have surgery, and sometimes other methods can be used to destroy kidney tumors. But there is much less information on how well these methods work over the long term and some doctors may still consider them to be experimental.

Cryotherapy (Cryoablation)

This approach uses extreme cold to destroy the tumor. A hollow probe (needle) is inserted into the tumor either through the skin or during laparoscopic surgery. Very cold gases are passed through the probe, creating an ice ball that destroys the tumor.

Radiofrequency Ablation (RFA)

This technique uses high-energy radio waves to heat the tumor. A thin, needle-like probe is placed through the skin and moved until the end is in the tumor. Once it is in place, an electric current is passed through the probe, which heats the tumor and destroys the cancer cells.

Arterial Embolization

This is a technique that blocks the artery feeding the kidney with the cancer. This method, which is rarely done, is sometimes used before surgery to kill some of the cancer cells and to reduce bleeding during the operation.

Radiation Therapy

Radiation therapy is treatment with high-energy rays (such as x-rays) to kill or shrink cancer cells. External radiation aims radiation from outside the body on the cancer. This type of treatment is sometimes used as the main treatment for kidney cancer for patients who cannot have surgery. It can also be used to ease symptoms such as pain, bleeding, or problems caused by the cancer spreading. But kidney cancer does not respond well to radiation. It is not often used before or after surgery because studies have shown that is doesn't help people live longer.

Radiation therapy is more often used to ease (palliate) symptoms of kidney cancer such as pain, bleeding, or problems caused by cancer spread (especially to the bones or brain).

Side effects of radiation can include mild skin changes that look like sunburn, nausea, diarrhea, or tiredness. Often these go away after a short while. Radiation can also make the side effects of chemotherapy worse. Radiation to the chest area can cause lung damage and lead to trouble breathing and shortness of breath. Side effects of radiation to the brain usually become most serious 1 or 2 years after treatment and can include headaches and trouble thinking.

Targeted Therapies

As researchers have learned more about the gene changes in cells that cause cancer, they have been able develop newer drugs that specifically target some of these changes. These targeted drugs work in a different way than standard chemotherapy drugs, and they have different side effects.

In the past few years several targeted drugs have been approved by the FDA for use against advanced kidney cancer. Targeted therapies include drugs that stop the growth of the new blood vessels that feed cancers and drugs that stop other parts of cancer cell growth. They are often used as the first line of treatment against advanced kidney cancers. While they may shrink or slow the growth of the cancer, it's not yet clear if any of these drugs can cure kidney cancer.

Biologic Therapy (Immunotherapy)

Because chemotherapy for kidney cancer does not work very well, doctors are looking at a newer approach called biologic therapy. This is treatment that boosts the body�s own defense system to help fight off or destroy cancer cells. Up to now, this was the most common first treatment for advanced kidney cancer, and it may still be helpful for some people. Because biologic therapy can be hard to give and can cause serious side effects, some doctors now reserve it for people who have cancers that don't respond to targeted therapies.

The main immunotherapy drugs used in kidney cancer are cytokines (proteins that activate the immune system). For a small number of patients, cytokines can shrink the cancer to less than half its original size.

The side effects of immunotherapy can be severe and, rarely, fatal. For this reason, only doctors experienced in the use of cytokines should give this treatment to people with kidney cancer.

Chemotherapy

Chemotherapy (often called simply "chemo") is the use of anti-cancer drugs injected into a vein or given as a pill. These drugs enter the bloodstream and go throughout the body, making the treatment useful for cancers that have spread to distant organs. Unfortunately, kidney cancer does not usually respond well to chemotherapy.

Chemotherapy can have some side effects. These side effects will depend on the type of drug, how much you take, and how long you take it. Most of the side effects go away when treatment is over. Anyone who has problems with side effects should talk with their doctor or nurse.

Pain Control

Pain is a major concern for some people with advanced kidney cancer. Be sure to tell your doctor or nurse about any pain you are having. Unless they know about your pain, they can't help.

For most people, treatment with morphine or other opioids (the strongest pain medicines available) will work to control the pain. For the treatment to work best, the pain medicines must be taken on a regular schedule, not just when the pain becomes severe. Some long-acting forms of morphine and other drugs need to be taken only once or twice a day.

In some cases, surgery or radiation may be helpful in relieving pain caused by cancer spreading to certain areas. This is called palliative therapy. In people whose cancer has spread to the bones, drugs called bisphosphonates may also be helpful.

Kaposi Sarcoma

What Is Kaposi Sarcoma?

Kaposi sarcoma (KS) is a cancer that develops from the cells that line lymph or blood vessels. KS is caused by the Kaposi sarcoma herpesvirus (KSHV), which is also called human herpesvirus 8. Although people do not develop KS without first getting infected with KSHV, most people who are infected with KSHV never develop KS. Someone who is infected with KSHV is more likely to develop KS if their immune system doesn’t work properly. The most common immune system problem that contributes to KS is infection with the human immunodeficiency virus (HIV).

The abnormal cells of KS form purple, red, or brown blotches or tumors on the skin. These affected areas are called lesions. Although the skin lesions of KS may look bad, in many cases, the lesions cause no symptoms. In other cases, the disease causes painful swelling, especially in the legs, groin area, or skin around the eyes. KS can cause serious problems (or even become life threatening) when the lesions are in the lungs, liver, or digestive tract. KS in the digestive tract, for example, can cause bleeding, while tumors in the lungs may cause difficulty breathing.

Types of Kaposi sarcoma

Some cancers such as lung cancer or breast cancer have several different types that indicate either different types of cells have become cancerous or different types of changes have occurred within a particular cell type. On the other hand, the different types of KS are defined by the different populations it develops in, but the changes within the KS cells are very similar.

Epidemic (AIDS-related) Kaposi sarcoma

The most common type of Kaposi sarcoma (KS) in the United States is epidemic or AIDS-related KS. This type of KS develops in people who are infected with HIV, the virus that causes AIDS. A person infected with HIV (that is, who is HIV-positive) does not necessarily have AIDS. The virus can be present in the body for a long time, typically many years, before causing major illness. The disease known as AIDS begins when the virus has seriously damaged the immune system, which results in certain types of infections and other medical complications. When HIV damages the immune system, people who also are infected with Kaposi sarcoma herpesvirus are more likely to develop KS.

Treatment of HIV infection with highly active antiretroviral therapy (HAART) has decreased the incidence of epidemic KS and can often keep advanced KS from developing. Not everyone whose HIV is well controlled is protected from KS, and sometimes aggressive KS develops that requires the use of chemotherapy or other treatments. In areas of the world where HAART is not easy to obtain, KS in AIDS patients can advance quickly and cause death in just 6 months.

Classic (Mediterranean) Kaposi sarcoma

Classic Kaposi sarcoma (KS) occurs in elderly people of Mediterranean, Eastern European, and Middle Eastern heritage. Classic KS is more common in men than in women. Patients typically have one or more lesions on the legs, ankles, or the soles of the feet. In comparison with other types of KS, the lesions in this type do not grow as quickly, and new lesions do not develop as often. The people who get classic KS come from areas where KS herpesvirus infection is more common than in the US or Northern Europe. The immune system of people with classic KS is not as weakened as those who have epidemic KS. But, getting older may naturally weaken their immunity a little, which makes people more likely to develop KS if they already have a KS herpesvirus infection.

Endemic (African) Kaposi sarcoma

Endemic Kaposi sarcoma (KS) occurs in people living in Equatorial Africa and is sometimes called African KS. KS herpesvirus infection is much more common in Africa than in other parts of the world, increasing the chance of KS developing. There appear to be other factors in Africa that contribute to the development of KS since the disease affects a broader group of people that includes children and women.

Endemic KS tends to occur in younger people (usually under age 40). Rarely a more aggressive form of endemic KS is seen in children before puberty. This type usually affects the lymph nodes and other organs and can lead to death within a year.

Iatrogenic (transplant associated) Kaposi sarcoma

When Kaposi sarcoma (KS) develops in people whose immune systems have been suppressed after an organ transplant it is called iatrogenic, or transplant-associated, KS. Most transplant patients take drugs to keep the immune system from rejecting (attacking and killing) the new organ. These drugs weaken the body's defenses, and this increases the likelihood that people infected with KSHV will develop KS. Stopping the immune suppressing drugs or lowering their dose often makes KS lesions disappear or get smaller.

Do We Know What Causes Kaposi Sarcoma?


Kaposi sarcoma is caused by a virus called the Kaposi sarcoma herpesvirus (KSHV), also known as human herpesvirus 8 (HHV8). KSHV belongs to the herpesvirus family and is similar to Epstein-Barr virus, the virus that causes infectious mononucleosis ("mono") and contributes to several types of cancer. KSHV has to be present in the tumor cells of Kaposi’s sarcoma for it to develop. Endothelial cells, which are cells that line blood and lymphatic vessels, are infected with KSHV in KS. Although scientists do not yet completely understand how KSHV causes KS, they do know that the virus brings genetic material into the cells that causes them to divide too much and invade surrounding tissues.

KSHV infection is much more common than KS, and most people infected with this virus do not get KS. The percentage of people infected with KSHV is different in different places around the world. In the United States, studies have found infection rates ranging from 5% to 25% in different parts of the country, and KSHV is more commonly found in gay men.

In some areas of Africa, more than 90 % of the population shows signs of KSHV infection. In these areas the virus seems to spread from mother to child. KSHV is more commonly detected in saliva than in other body fluids. Many people infected with KSHV will never show any symptoms. A very small number of those infected will get a mild type of KS. In people whose immune systems are weakened (by AIDS, for example) infection with KSHV is much more likely to lead to KS.

Can Kaposi Sarcoma Be Found Early?

Most cancers start in one place and then spread to other parts of the body. When these cancers are found early, they are more likely to be curable. KS is very different. KS tends to form in several areas at the same time. Even when only 1 skin lesion is visible, many patients already have other areas of KS that are just too small to be seen.

People infected with HIV should be regularly examined by health care providers familiar with diagnosing KS and other manifestations of AIDS. Patients who are aware of the signs and symptoms of KS and other AIDS-related problems should tell their doctors so they can receive treatment promptly, if they need it.

How Is Kaposi Sarcoma Treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.

The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.

Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.

Treatment for KS is more effective than it was a couple of decades ago. Doctors now better understand what causes KS. Many clinical trials have been done to compare different approaches to treatment. Doctors have much more experience with KS than they did when this disease was quite rare. Choices about the best treatment options for each patient are based on the function of the immune system as well as the number, location and size of the KS lesions. The patient's general condition is also a major factor. The presence and severity of other serious medical conditions can make some treatments a poor choice. Some of the treatments used for KS are surgery, chemotherapy, radiation therapy, and biological therapy. In some cases, 2 or more of these treatments are used together.

Treating immune deficiency and related infections

The most important treatment for KS is to treat any immune deficiency that exists as well as any related infections. In people with AIDS, this means using highly active antiretroviral therapy (HAART) (specific anti-HIV drugs). For many AIDS patients with KS, HAART may be the only treatment needed. for the KS. In organ-transplant patients who are immune suppressed because they are taking medicines, decreasing or changing the drugs may be helpful. New KS lesions are more likely to develop when a patient's blood test results for KS herpesvirus (KSHV) are positive. The risk of developing new lesions is lower when antiviral medicines such as ganciclovir or foscarnet are used. In contrast, existing lesions are relatively resistant to treatment with antiviral agents. KS lesions tend to get worse when patients develop infections with bacteria. Therefore, it is very important to take measures to prevent bacterial infections and to treat them promptly and effectively if they do occur.

Hodgkin Disease

What Is Hodgkin Disease?

Hodgkin disease (or Hodgkin lymphoma) is a type of lymphoma. There are 2 kinds of lymphoma:

  • Hodgkin disease (named after Dr. Thomas Hodgkin, who recognized it in 1832)

  • non-Hodgkin lymphoma

Non-Hodgkin lymphoma is covered in a separate American Cancer Society document.


The Lymph System and Lymphoid Tissue


To better understand Hodgkin disease, it helps to know about the body's lymph (pronounced "limf") system. The lymph system is made up of lymphoid tissue, lymph vessels, and a clear fluid called lymph.

Lymphatic tissue includes the lymph nodes and other organs that are part of the body�s immune and blood-forming systems. Lymph nodes are small, bean-shaped organs found in many places throughout the body. Other parts of the lymphatic system include the spleen, the bone marrow, and the thymus gland.

The lymph nodes make and store lymphocytes, which are special white blood cells that fight infection. There are 2 types of lymphocytes: B lymphocytes (or B cells) and T lymphocytes (or T cells). Most cases of Hodgkin disease start in B lymphocytes.


Start and Spread of Hodgkin Disease


Because lymphatic tissue is found in many parts of the body, Hodgkin disease can start almost anywhere. Most often it starts in lymph nodes in the upper part of the body. (Those in the chest, neck, or under the arms.) This disease causes the lymphatic tissue to become enlarged and press on nearby structures. But lymph nodes can become swollen for many reasons. Most often it happens when the body is fighting an infection.

Hodgkin disease can spread through the lymphatic vessels in a stepwise fashion from lymph node to lymph node. Rarely, and late in the disease, it gets into the blood vessels and can then spread to almost any other place in the body.


The Hodgkin Disease Cell


The cancer cells in Hodgkin disease are unique. They are called Reed-Sternberg cells (or Hodgkin cells). They are an abnormal type of B lymphocyte that is much larger than normal lymphocytes.

The 2 main types are classical Hodgkin disease (which has several subtypes) and nodular lymphocyte predominance Hodgkin disease. The types differ in the way the cancer cells look under a microscope. The types are important because each grows and spreads in a different way. Often they are treated differently. Ask your doctor about the exact type of Hodgkin disease you (or your loved one) has.


Classical Hodgkin Disease


Classical Hodgkin disease (HD) accounts for about 95% of all cases of Hodgkin disease in developed countries. It has 4 subtypes, all of which have Reed-Sternberg cells that can be seen under the microscope.


Nodular Lymphocyte Predominant Hodgkin Disease


Nodular lymphocyte predominant Hodgkin disease (NLPHD) accounts for about 5% of Hodgkin disease. This type mostly involves lymph nodes in the neck and under the arm.

All types of Hodgkin disease are cancerous (malignant) because as they grow they may compress, invade, and destroy normal tissue and spread to other tissues. Hodgkin disease occurs in both children and adults. Because Hodgkin disease is similar in both children and adults, this document covers treatment in both groups.

What Causes Hodgkin Disease?

We do not yet know exactly what causes Hodgkin disease, but we do know that certain risk factors are linked to the disease. A risk factor is something that affects a person's chance of getting a disease such as cancer. Different cancers have different risk factors. Some risk factors, such as smoking, can be controlled. Others, like a person's age or family history, can't be changed. But having a risk factor, or even many, doesn't mean that a person will get the disease. Likewise, not having any risk factors doesn't mean a person won't get the disease.

Scientists have found a few risk factors that may make a person more likely to get Hodgkin disease, although it's not always clear why these factors increase risk.


Epstein-Barr Virus (EBV) Infection/Mononucleosis

There is a higher risk of Hodgkin disease among people who have had "mono" (infectious mononucleosis), caused by the Epstein-Barr virus. The risk is a few times higher in people who have had this disease, although the overall risk is still very small.


Age

Hodgkin disease is most common in early adulthood (age 15 to 40, especially in a person's 20s) and in late adulthood (after age 55).


Gender

Hodgkin disease occurs slightly more often in males than in females.


Geography

Hodgkin disease is most common in the United States, Canada, and northern Europe, and is least common in Asian countries.


Family History

There is a higher risk for Hodgkin disease in brothers and sisters of young people with this disease. The risk is very high for an identical twin of a person with Hodgkin disease.


Socioeconomic Status

The risk of Hodgkin disease is greater in people with a higher socioeconomic background.


Can Hodgkin Disease Be Prevented?

Since we do not know what causes Hodgkin disease, it is not possible at this time to prevent the disease.

How Is Hodgkin Disease Found?

There are no tests to find Hodgkin disease early, and some people with the disease have no symptoms at all. Most people with Hodgkin disease see their doctor because they have felt a lump that hasn't gone away or they just don't feel well and go in for a check-up. They may have a swollen lymph node in the neck, arm pit, or groin area. Sometimes it will go away only to come back. Eventually, it doesn't go away, and though it doesn't hurt, it will get larger and cause the person to go to the doctor.

But in most people, especially children, enlarged lymph nodes are caused by an infection or other illness and not cancer. If you (or your child) have lymph nodes over an inch in size and no recent infection, it is best to have them checked by the doctor.


Signs and Symptoms of Hodgkin Disease

You or your child can have Hodgkin disease and feel perfectly well. However, there are some symptoms that this disease may cause.


Lumps Under the Skin

You may notice a lump in the neck, under the arm, or in the groin. Sometimes this may go away, only to come back. Although it doesn't hurt, it may finally not go away, and lead you to see a doctor.


General Symptoms

Some patients with Hodgkin disease have fever, drenching night sweats, or weight loss. The fever can come and go over many days or weeks. Itching, tiredness, and poor appetite are other symptoms that may occur. Sometimes the only symptom may be feeling tired all the time. However, infections, other types of cancer, or other conditions can also cause these symptoms.


Cough or Trouble Breathing

When Hodgkin disease affects lymph nodes inside the chest, the swelling of these nodes may press on the windpipe. This can make you cough or even have trouble breathing, especially when lying down.

If you or your child has any of these symptoms, discuss them with your doctor right away. The sooner a correct diagnosis is made, the sooner treatment can be started and the better the treatment will work.


Medical History and Physical Exam

If symptoms suggest that you might have Hodgkin disease, the doctor will want to get a complete medical history, including how long you have had the symptoms. The doctor will ask questions about your health now and in the past and to do a physical exam to see whether there is an infection. During the exam, the doctor will pay special attention to the lymph nodes. Because it is common for people, especially children, to have swollen lymph nodes, the doctor will look for infection first. If the doctor thinks that Hodgkin disease might be causing the symptoms, he or she will want to do a biopsy.

Biopsy

A biopsy involves removing a sample of the lymph node and looking at it under a microscope. This is the only way to know for sure if the swelling is caused by cancer. There are many different kinds of biopsies, and the doctor will choose the one best suited for you or your child. The goal is to get enough tissue to be sure of the diagnosis.

Some biopsies involve cutting through the skin to remove an entire node or a small part of a larger tumor. If the node is near the surface of the skin, the skin can be numbed and the sample taken. But if the node is deeper inside the body, the patient may need to be asleep first.

In a less common type of biopsy, the doctor uses a thin needle to remove a small amount of fluid and tiny bits of tissue from the tumor.

Lab Tests

A doctor with special training in blood and lymph tissue disease (called a pathologist) looks at all biopsy samples under a microscope. The doctor looks at the appearance, as well as the size and shape of the cells to find out whether any of them are Reed-Sternberg cells. Sometimes the first biopsy does not provide a definite answer and more biopsies are needed.

Looking at the tissue under the microscope can often tell whether you have Hodgkin disease and what type it is, but sometimes special stains are used on the sample to provide more information.

How Is Hodgkin Disease Treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.

The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.

Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.


This section first describes the types of treatments used for Hodgkin disease. Then the treatment options based on the stage of the disease (as well as other factors) are explained.

In recent years, much progress has been made in treating Hodgkin disease. Most people can be cured with chemotherapy and radiation therapy. Treatment is based on the stage and type of the disease, but a person�s age, overall health and other factors may be taken into account as well.


Making Treatment Decisions

After Hodgkin disease is staged, the doctor will discuss treatment choices with you. It is important to take time and think about all the choices. Be sure that you understand all the risks and side effects before making a decision. Getting a second opinion can give you more information and help you feel more confident in the treatment you choose.

For nearly all people with Hodgkin disease, complete cure is the main goal. The two main methods of treating Hodgkin disease are chemotherapy and radiation therapy. Sometimes both treatments are used. High dose chemotherapy with blood-forming stem cell transplants, discussed later, is used for certain people. For the most part, surgery (except for biopsy and staging) is not part of the treatment of Hodgkin disease.


Chemotherapy

Chemotherapy (often called simply "chemo") refers to the use of drugs to kill cancer cells. Usually the drugs are given into a vein or by mouth (as pills). Once the drugs enter the bloodstream, they spread throughout the body. Several drugs are given at the same time to treat Hodgkin disease.

Although the chemo kills cancer cells, the drugs also damage normal cells. This can lead to side effects. The exact side effects depend on the type and dose of drugs used and the length of time they are taken. Side effects could include the following:

  • hair loss
  • mouth sores
  • loss of appetite
  • nausea and vomiting
  • increased chance of infections (due to low white blood cell counts)
  • easy bruising or bleeding (due to low blood platelet counts)
  • fatigue (due to low red blood cell counts)

These side effects are usually short-term and go away after treatment is finished. There are often ways to lessen these side effects. For example, drugs are usually given to help prevent or reduce nausea and vomiting. If you or your child has side effects, talk to your cancer care team. They can suggest steps to ease them.

If white blood cell counts are very low during treatment, you can help reduce the risk of infection by carefully avoiding exposure to germs. During this time, your doctor may advise you to:

  • Wash your hands often.
  • Avoid fresh, uncooked fruits and vegetables and other foods that might carry germs.
  • Avoid fresh flowers and plants because they may carry mold.
  • Make sure other people wash their hands before they come in contact with you.
  • Avoid large crowds and people who are sick (wearing a surgical mask offers some protection in these situations).

Some chemo drugs can have side effects that occur long after treatment has ended. These can affect a person's heart, lungs, growth, and ability to have children. There is also an increased risk of developing a second type of cancer, especially if chemo and radiation are given at the same time. It's important to discuss these possible side effects with the doctor before treatment begins. If the patient is old enough and is going to receive drugs that cause sterility, sperm banking should be discussed before treatment is started.


Radiation Therapy

Radiation therapy is the use of high-energy x-rays to destroy cancer cells. When radiation therapy is given for Hodgkin disease, it usually involves a focused beam of radiation, given from a machine outside the body. This is known as external beam radiation. Radiation is used along with chemotherapy when the Hodgkin disease involves a large or bulky tumor mass, usually in the chest

Doctors have found that in some cases, treating only the known areas of disease with radiation may also produce a cure. This is called involved field radiation and is now the preferred form of radiation therapy when used along with chemo, although they are not given at the same time. Chemo is given first, followed by involved field radiation given to areas that showed cancer.

Radiation therapy can cause some serious side effects including damage to nearby healthy tissue. Other problems can include skin changes similar to sunburn, tiredness, upset stomach, and diarrhea.

In the past, radiation was thought to have fewer side effects than chemo. But as more patients have been able to live out their normal life spans after successful treatment for Hodgkin disease, more long-term problems from radiation have been seen. Radiation to the chest leads to an increased risk of heart disease (such as heart attacks). Radiation to the neck may increase the risk of stroke many years later. Because of these problems, doctors are slowly moving away from using radiation, or at least limiting the dose and areas of the body that are treated.


High-Dose Chemotherapy and Bone Marrow or Peripheral Blood Stem Cell Transplant

Standard doses of chemo drugs can cause serious side effects to quickly dividing tissues such as the bone marrow. Although even higher doses of these drugs might work better to treat Hodgkin disease, they are not given because the severe damage to bone marrow cells would cause lethal shortages of blood cells, and other vital organs would likely be damaged too.

But sometimes Hodgkin disease does not respond well to standard treatment, or the disease comes back later. In these cases, a stem cell transplant (SCT) allows doctors to use higher doses of chemo. After treatment is finished, the patient receives a transplant of blood-forming stem cells to restore the bone marrow.


Autologous Stem Cell Transplant

For this type of transplant, blood-forming stem cells from the patient�s own blood (or, less often, from the bone marrow) are removed, frozen, and stored. Then very high doses of chemotherapy (with or without radiation therapy) are given in order to kill the cancer. These high doses destroy bone marrow, too. When that happens, the body is no longer able to make new blood cells. So, after the treatment, the stored stem cells are thawed and given back to the patient through a vein. The cells enter the bloodstream and return to the bone, replacing the marrow and making new blood cells.

(If this type of transplant fails, then a matched donor might supply the stem cells. When the stem cells come from someone else it is called an allogenic stem cell transplant.)


The Transplant Process

The treatment works like this: stem cells are collected from the bloodstream in a process called apheresis. The cells are frozen and stored. Patients are then given very high doses of chemo to kill the cancer cells. The patient might also receive total body radiation to kill any remaining cancer cells. After treatment, the stored stem cells are given to the patient like a blood transfusion. The stem cells settle into the patient's bone marrow over the next several days and start to grow and make new blood cells.

People who receive a donor's stem cells are given drugs to prevent rejection. Usually within a couple of weeks after the stem cells are given, they start making new white blood cells. Then they begin making platelets, and finally, red blood cells.

Patients having SCT have to be kept away from germs as much as possible until their white blood cell count is at a safe level. They are kept in the hospital until the white cell count reaches a certain number, usually around 1,000. After they go home, they will be seen as an outpatient regularly for about 6 months.


Some Things to Keep in Mind

Stem cell transplantation is a complex treatment. If the doctors think that a patient might be helped by this treatment, it is important that it be done at a hospital where the staff has experience with the procedure. Some transplant programs may not have experience in certain transplants, especially those from unrelated donors.

Stem cell transplant is very expensive (more than $100,000) and often involves a long hospital stay. Because some insurance companies see it as an experimental treatment, they might not pay for it. It is important to find out what your insurance will cover and what you might have to pay before deciding on a transplant.


"Mini Transplant"

Most patients over the age of 55 can't have a regular transplant that uses high doses of chemo. Some may be able to have what is called a "mini-transplant" (a non-myeloablative transplant or reduced-intensity transplant), where they get lower doses of chemo and radiation which do not destroy all the cells in their bone marrow. They then are given the donor stem cells. These cells enter the body and form a new immune system, which sees the cancer cells as foreign and attacks them (a "graft-versus-lymphoma" effect). To learn more about stem cell transplants, see the American Cancer Society document, Bone Marrow & Peripheral Blood Stem Cell Transplants.


Side Effects of Stem Cell Transplant

Side effects from stem cell transplant can be divided into short- and long-term effects. The short-term or early side effects are about the same as those caused by any other type of high-dose chemo. One of the most common and serious short-term effects is the greater risk of infection. Other side effects include low red blood cell counts, nausea, vomiting, loss of appetite, mouth sores, and hair loss.


Long-term Side Effects

Some side effects can last for a long time, or may not happen until years after the transplant. These long-term side effects can include the following:

  • graft-versus-host disease (GVHD), which occurs only in a donor (allogeneic) transplant (see below)
  • infertility
  • early menopause
  • radiation damage to the lungs, causing shortness of breath
  • damage to the thyroid gland that causes problems with changing food into energy
  • cataracts (damage to the eye that can affect vision)
  • damage to the lungs, causing shortness of breath
  • bone damage (if damage is severe, the patient will need to have part of the bone and joint replaced)
  • getting leukemia several years later

Graft-versus-host disease is the main problem of a donor stem cell transplant. It happens when the immune system of the patient is taken over by that of the donor. The donor immune system then starts to attack the patient�s other tissues and organs.

Symptoms can include severe skin rashes with itching and severe diarrhea. The liver and lungs may also be damaged. The patient may also become tired and have aching muscles. If severe enough, the disease can be fatal. Drugs that weaken the immune system may be given to try to control it. On the plus side, this disease also causes any remaining lymphoma cells to be killed by the donor immune system. Mild graft-versus-host disease can be a good thing.



Hodgkin Disease in Children

The types of Hodgkin disease that develop in children are generally different from the types that are found in adults. In most cases, childhood cancers tend to respond better to chemo. Children's bodies also tend to tolerate chemo better than adults. But because chemotherapy can have some long-term side effects, children who survive their cancer need careful attention for the rest of their lives.


Treatment Differences

Although the treatment for Hodgkin disease is generally the same for adults and children, there are some differences. If the child is older, the treatment is often the same as that given to adults. But if the child's body is still growing, then the doctor is more likely to use chemo instead of radiation because radiation can affect bone and muscle growth. The goal of treatment for children is to cure the cancer without causing long-term problems.

Since radiation treatment in large doses can keep children from reaching their normal size, when children with Hodgkin disease are treated with radiation the dose is kept low. In order to cure children, doctors often combine radiation in low doses with chemotherapy. The success of this approach has been very good. Cure rates for children can reach 85% to 100%, even with more advanced disease.


Childhood Cancers Are Treated at Special Centers

Children (and teenagers) with cancer and their families have special needs that are best met by children�s cancer centers that work closely with the child�s main doctor. These centers offer the advantage of a team of experts with experience in treating children. They know the unique needs of children with cancer. The team can include (besides doctors and nurses) psychologists, social workers, child life specialists, educators, and others.

Since the 1960s most children with cancer in the United States have been treated at these special centers. Most children with cancer are treated at a children�s cancer center that is a member of the Children�s Oncology Group (COG). These centers are linked to either a medical college or a children�s hospital.


Resistant Hodgkin Disease

Treatment for Hodgkin disease should get rid of all traces of the cancer. If tests still show some disease after treatment, many experts think that more of the same treatment will not cure the disease. Sometimes, radiation to a single area of disease that remains after chemo might work. Sometimes if radiation has failed, using chemo might be an option. But if both have failed, most doctors would recommend a stem cell transplant, if possible.


Recurrent Hodgkin Disease

The treatment for Hodgkin disease that comes back (recurs) depends on where the disease shows up and which treatment was used before. If the first treatment was just radiation therapy, then chemo would usually be given. If chemo had been used first, and the cancer came back only in the lymph nodes, then radiation therapy, with or without more chemo, could be given to the lymph nodes.

Although chemo with different drugs can be used for people with recurrent disease, radiation usually cannot be given again in the same area. For example, if someone had Hodgkin disease in the chest that had been treated with radiation, more radiation could not be used if the disease came back there. This is the case no matter how much time has gone by.

If the Hodgkin disease has returned within a few months of the first treatment, high-dose chemo with stem cell transplantation might be an option. On the other hand, if the disease has returned after a long time, then giving different chemo drugs might work. These are decisions that need to be made by you and your doctor.


Hodgkin Disease in Pregnancy

If a pregnant woman has Hodgkin disease, there are many options. In about half of all cases, a woman can wait until the baby is born and then begin treatment. This approach is safest for the baby.

If treatment needs to begin right away, one (or many) chemotherapy drugs may be given, depending upon the situation. Radiation is often not given, because of concerns about the long-term effects to the unborn baby. However, there have been a few studies of radiation as a treatment for pregnant women with Hodgkin disease. These studies suggest that as long as very careful measures are taken to aim the radiation precisely and limit the doses used, pregnant women with Hodgkin disease in the lymph nodes in the neck, arm pit, or inside the chest may be able to have this treatment with little or no risk of birth defects or childhood cancer.

HIV Infection and AIDS

What Is HIV/AIDS?

Acquired immunodeficiency syndrome, better known as AIDS, is caused by infection with a virus known as human immunodeficiency virus (HIV). AIDS is the most advanced stage in the course of HIV infection. The virus attacks and destroys the body's immune system (the system that protects the body from disease). Without a fully working immune system, a person is at risk for getting other infections that usually do not affect healthy people. These are called opportunistic infections. There is also a greater risk of getting certain types of cancer, such as Kaposi sarcoma, lymphomas, and cervical cancer, as well as other cancer types. Many of these conditions can be life threatening.

The first cases of AIDS in the United States were reported in 1981. They were noted and described as a rare form of pneumonia in otherwise healthy homosexual men. A blood test for HIV infection was developed and approved in 1985. Around that same time, the virus was found worldwide.

What Causes AIDS?


The cause of AIDS is the human immunodeficiency virus (HIV). The virus was not known to cause AIDS until 1983.

The type of HIV responsible for most AIDS cases in the United States and Europe is called HIV-1. There is a second virus found mainly in Africa called HIV-2. Even though we commonly call the virus HIV in the United States, it is called HIV-1 in medical labs.

HIV transmission

HIV can be transmitted from one person to another when blood or certain body fluids (vaginal secretions, semen, or breast milk) from an infected person get into an uninfected person. Routes of transmission have included:

  • unprotected vaginal, anal, or oral sex with an infected person
  • needles and drug equipment shared with injection drug users who have HIV
  • prenatal (before birth) and perinatal (during and right after birth) exposures of infants whose mothers are infected with HIV
  • breast-feeding by mothers with HIV
  • transfusion of blood products containing the virus
  • organ transplants from HIV infected donors
  • penetrating injuries or accidents of health care workers (usually needlesticks) while caring for HIV-infected patients or handling their blood

HIV is not spread by mosquitoes, ticks, or other insects. It can't be spread by casual contact such as talking, shaking hands, hugging, sneezing, sharing kitchen utensils or dishes, sharing bathrooms, sharing telephones or computers, or through water.

How Is HIV/AIDS Diagnosed?

People often believe that if they have had a physical exam, the doctor has checked for HIV. This is not usually true. Most of the time, HIV testing is not done unless you ask for it or have a medical situation that calls for testing. This may be changing, however. In late September 2006, the CDC issued guidelines for health care providers to begin routinely testing their patients aged 13 to 64 for HIV infection. The guideline noted that doctors were no longer required to counsel patients before the test.. Instead, the doctor should let the patient know that HIV testing will be included in routine blood testing. It is important to know that not all doctors follow guidelines such as this one. You may want to ask your primary care doctor whether his or her office performs routine HIV testing.

HIV testing is still more likely to be done if you have symptoms that look like AIDS, or if you are pregnant. The doctor or nurse will usually let you know that the test will be included along with other blood work. It is still fairly unusual for a person to be tested and not know it. There are a few cases where people are not told they are getting an HIV test. For instance, prisoners entering the penal system, people entering military service, and some people who apply for individual health or life insurance policies may be tested without knowing about it.

If you have any doubt about your HIV status, you might want to talk with your doctor or visit a health department clinic where testing is offered. To have the HIV test done without giving your name and address (anonymous testing), you can buy a home collection kit at the drugstore or go to a health department clinic that offers such testing. Most state health departments and a few other health sites offer anonymous HIV tests.

Because HIV infection often has no symptoms for years, a person can have HIV for a long time and not know about it until he or she is tested. People who do not seek HIV testing may not learn that they have HIV until they develop early symptoms or even AIDS. With proper testing, however, HIV infection can be detected easily and treated sooner.

Tests to detect HIV infection

HIV testing is available in many settings (hospitals, neighborhood clinics, health department clinics, doctors' and offices). HIV test kits that can be used at home are even available..

Understanding lab tests and results

Depending on where the test is done, it can take a few days to 2 weeks to get the results. Nearly all testing locations require that you return in person for your test results. Telephone results are usually given only for home kit testing, after the blood sample you mailed in is tested.

HIV is most often found using a pair of screening tests that look for antibodies to HIV in the blood. When the body is infected with HIV, it starts to make antibodies (immune system proteins) against the virus. Although these antibodies are not effective in getting rid of HIV, they can be found in the blood and some other body fluids within several weeks of infection. HIV tests look for these antibodies, not the virus itself (which would be much harder to detect).

In the United States, the first test used in most cases is called the HIV enzyme-linked immunosorbent assay (ELISA or EIA). This is a very sensitive test that can find antibodies to HIV in the blood. Because it is so sensitive, it sometimes finds "look-alike" substances that are not due to HIV, yielding a positive result in some people who may not have HIV. This is why a second test is used to confirm a positive ELISA test. This second test, known as a Western blot test, is done on the same sample of blood or body fluid.

If the ELISA test finds nothing, the HIV test result is reported as negative. This means that no trace of antibodies to HIV could be found. No further tests on the sample are needed.

If the ELISA result is positive, it is checked by using a more specific test, usually the Western blot test. If this test result is negative, it is very likely that the ELISA test gave a "false positive" result. The HIV test result is reported as negative, since antibodies to HIV were not found on this more specific test.

If both test results are positive, it means that the person is infected with HIV.

In rare cases, the Western blot test results come back not as positive or negative, but "indeterminate" (the test cannot tell if it is positive or negative). Sometimes, an indeterminate test means that the person has recently been infected with HIV but does not yet have enough antibodies to be sure. Most of the time, an indeterminate test result is caused by an unrelated condition. Because of this, people who have indeterminate results usually repeat the HIV test a few weeks later to find out whether they are actually infected.

The possible test results are outlined in the table below.

Table 1. How ELISA and Western Blot tests determine final HIV antibody test results

Treatment ELISA
result
Western Blot
Result
Negative Not done Negative HIV test
Positive Negative Negative HIV test
Positive Positive Positive HIV test
Positive Indeterminate Indeterminate HIV test

It's important to note that a negative test result does not mean for sure that a person does not have HIV. It takes several weeks after becoming infected with the virus before enough antibodies are produced to be detected. To be sure that the person doesn't have the virus, he or she should be tested 3 to 6 months after the most recent suspected exposure.

Other lab tests: Other types of lab tests may be used to test for HIV. In general, these tests are used only in certain situations, such as when testing newborns (see section below).

  • indirect immunofluorescence assay (IFA): For this test, a fluorescent dye is used to detect HIV antibodies in the blood.
  • viral culture methods: Viral culture tests involve growing live HIV from infected cells. Viral culture was the first method ever used to detect the HIV virus itself instead of the antibody response, but it is slow and expensive.
  • polymerase chain reaction (PCR): PCR is a very sensitive test by which the genes of a cell are increased many times to detect HIV viral DNA or RNA. This allows the PCR to look for the virus rather than the antibodies.

Types of tests for HIV

Blood test: This is the most common way to test for HIV. A blood sample is taken in a doctor's office, clinic, hospital, etc., and is tested with an ELISA test. If this is positive, a Western blot test is done on the same sample. Results usually take a few days to 2 weeks.

Oral fluid test: This test looks for HIV antibodies in fluid taken from the mouth. For this test, a special test pad is placed between the cheek and the gum for about 2 minutes. The pad absorbs fluid from the bloodstream through the membranes of the cheek. The sample is then analyzed by the ELISA test and confirmed, if needed, by the Western blot test. It may take a few days to 2 weeks to get these results.

Urine test: HIV antibodies are also present in small amounts in the urine. Thus, an ELISA-type test and Western blot test have been developed to detect HIV in the urine. Getting this test result also takes a few days to 2 weeks, depending on the lab.

Quick test: In 2004, the Food and Drug Administration (FDA) approved a faster test, the OraQuick Rapid HIV-1 Antibody Test. It is only used by trained staff, but it can detect antibodies to HIV in blood from a finger stick and provide results in less than 20 minutes. Positive results must be confirmed with a separate Western blot test, which can take several days after the second blood sample is taken. Negative results require no further testing (unless possible HIV exposure was recent and antibodies haven't had time to develop). The quick test is only offered in certain settings where specialized counseling and follow up tests can be done for people with positive results. This test can also be done on fluid taken from the mouth.

Home tests: There is also a home test approved by the FDA. There are a few HIV home test kits being advertised on the market today, but as of 2007 only the Home Access test system is FDA approved and legally marketed in the United States. The Home Access test has many pieces, including materials for specimen collection, a mailing envelope to send the specimen to a lab, and pre- and post-test counseling information.

This approved system uses a simple finger-stick process to collect blood at home. Blood is placed on a special paper in the kit and allowed to dry. The paper with the dried blood is mailed to a lab along with a personal identification number (PIN). It is tested by trained technicians in a certified medical lab the same way as samples taken in a doctor's office. The person who mailed in the test can call the toll-free number and give the PIN number to get their results and post-test counseling.

There are also home tests that are not FDA approved. These are advertised and sold in newspapers, magazines, and on the Internet, and often falsely claim that the tests are FDA approved or "manufactured in an FDA-approved facility." The advertisers of the unapproved HIV home test kits often claim that the presence of a visible sign, such as a red dot, within 5 to 15 minutes of taking the test shows a positive result for HIV infection. These unapproved test kits may use a finger-stick process to collect blood or a sponge for collecting saliva.

The blood or saliva sample is then placed in a plastic testing device containing some type of paper. A developing solution is added to find out if the sample is positive. The samples are not sent to a lab for professional testing. In 1999, the US Federal Trade Commission tested some samples of infected blood using unapproved test kits. All of the known HIV-positive blood samples tested negative. Although unapproved home tests may seem simpler and faster, they can give unreliable results. If you would like to know if a particular HIV test has been approved by the FDA, you can check their information sheet on the Internet at www.fda.gov/CbER/infosheets/hiv-home2.htm, or you can call them at 1-800-835-4709. You can also email them at octma@cber.fda.gov.

Testing newborns: Antibody tests are not helpful in newborns whose mothers are known to have HIV. Babies are born with their mothers' antibodies, which stay with them for several months. This means that any baby born to an HIV-infected mother will test positive for antibodies to HIV. This can be very confusing, because it means an infant's blood can test HIV-positive when the baby is not actually infected. Rather than wait a year or more for all of the mother's antibodies to go away, tests that detect the virus are used to find out whether an infant got HIV from its mother. It is important to find out quickly, because newborns with HIV can be treated early to help keep them from getting sick. Even with these tests, it may still take a few weeks to be certain of the infant's true HIV status.

Tests to diagnose AIDS and measure immune function

A diagnosis of AIDS is made when a person is shown to have HIV and impaired immune function. Impaired immunity is shown by certain opportunistic infections or cancers (see "The definition of AIDS" section), or when lab tests for CD4 cells show poor immune function. These kinds of tests are usually only done for those who are known to have HIV. People with HIV are tested every few months to help decide when to start treatment. They are also tested regularly after anti-HIV drugs are started, to be sure that the drugs are working as expected.

If a person has been diagnosed with AIDS based on a positive HIV test and a low CD4 count, he or she is still considered to have AIDS even if treatment later raises the CD4 count. If a person is diagnosed with AIDS based on a positive HIV test and having an AIDS-defining condition, he or she still has AIDS even if the AIDS-defining condition is later cured.

Immune profile, including CD4 counts: An immune profile, or immune panel, is a blood test that can be used to measure the loss of immunity and help decide on the best treatment. This profile usually includes counts of different types of cells in the blood (a complete blood cell count, or CBC). More important, it counts the number and percentage of CD4+ T lymphocytes. These are more commonly called CD4 cells, helper T cells, or T cells (see the section "The normal immune system").

The number of CD4 cells reflects the patient's stage of infection and is used to find out how much damage HIV has done to the immune system. It counts the number of CD4 cells in each cubic millimeter (mm3) of blood. A normal count in a healthy, HIV-negative adult can vary but is usually between 500 and 1,500 cells/mm3. (In babies and very young children the normal CD4 counts are much higher.) HIV infection lowers the CD4 count. People begin to get opportunistic infections or cancers more often as the count drops.

Viral load test (HIV-1 RNA): This test measures the amount of HIV that is found in a small amount of blood (the "viral load"). The viral load test is done after a patient has tested positive for HIV. Unlike the immune panel, this test does not show how much damage has been done to the immune system, so it cannot show whether a person has AIDS. It can show how quickly the HIV infection is likely to progress, however. A high viral load, even in a person with good T cell counts, suggests that the person may worsen quickly and become AIDS if not treated.

The viral load test is also often used to find out how well an infected person is responding to treatment. Doctors look for the viral load to go down and stay down while a person is taking anti-HIV drugs.

Viral load testing is done using polymerase chain reaction (PCR) or other lab techniques (see above). It is not normally used to find out if a person has HIV, because of its cost and other limitations. Sometimes, however, a week or two after being exposed, a person may start having symptoms that suggest early HIV (see Primary infection in the "The course of the disease" section). Because an HIV antibody test will probably not become positive for a few more weeks, a viral load is one kind of test that may be used right away in this unusual situation to find out if HIV is present. It is sometimes also used to diagnose infants who are born to HIV-infected mothers.

How Is HIV/AIDS Treated?

This information represents the views of the doctors and nurses serving on the American Cancer Society's Cancer Information Database Editorial Board. These views are based on their interpretation of studies published in medical journals, as well as their own professional experience.

The treatment information in this document is not official policy of the Society and is not intended as medical advice to replace the expertise and judgment of your cancer care team. It is intended to help you and your family make informed decisions, together with your doctor.

Your doctor may have reasons for suggesting a treatment plan different from these general treatment options. Don't hesitate to ask him or her questions about your treatment options.

First, find a doctor or clinician who has experience in treating people with HIV and AIDS. It is helpful to find someone you can talk to and feel safe with, since you will be seen fairly often. Even if you are not taking any prescribed HIV drugs, you will need to visit every 3 to 6 months for lab work and health checks.

Goals of treatment

Current treatment for HIV/AIDS has 3 main goals:

  • restore and preserve immune function
  • keep the amount of HIV in the body as low as possible for as long as possible
  • prevent, cure, or control opportunistic infections

All of these help to support quality of life by improving health and lowering the chance of serious illnesses and their long-term effects.

Restoring and preserving the immune system: This is done is by using drugs that help stop HIV growth. In slowing viral growth in the body, the drugs also greatly help restore and preserve the immune system. This helps reduce the risk of some types of AIDS-related cancers. CD4 counts are checked often to be sure the drugs are working.

Other measures that can be taken to support the immune system involve good self-care, such as better nutrition, exercise, and stress management, and stopping tobacco or illicit drug use. Vaccines are usually recommended to prevent influenza (the flu), certain types of pneumonia, and some types of hepatitis. These work better if given before the CD4 count goes very low. There are some types of vaccines that people with HIV should not take. Be sure to talk with your doctor before you or any of the people you live with are vaccinated.

Keeping HIV levels in the body as low as possible for as long as possible: This is also done by using anti-HIV drugs. This treatment is usually started after the infection has damaged the immune system to the point that that the person is about to risk having a serious illness. Many studies have shown that effective anti-HIV drugs reduce illness and prolong life.

Before starting anti-HIV treatment, the doctor checks the immune system, tests for anti-retroviral resistance (see "Treatment problems with HAART" below), tests for suspected opportunistic infections, and looks for other diseases or conditions that could change the treatment. Counseling, education, and emotional and social support are normally offered as part of HIV care.

Preventing, curing, or controlling opportunistic conditions: You may be able to prevent some infections by avoiding exposure. For instance, your doctor may suggest avoiding large crowds and close contact with people who have fevers or other signs of infection. You can avoid other infections by preparing foods in ways that kill germs or keep them from growing. The risk of some infections may be lowered by letting someone else clean your aquariums, cat litter boxes, and bird cages. As a person's CD4 count drops below certain levels, however, antibiotics may be needed to prevent certain serious illnesses such as AIDS-related pneumonia. (See the section on "Prevention and treatment of opportunistic infections," and Table 2, Preventing Exposure and Illness Due To Infection in People with HIV/AIDS, showing CD4 counts.)

Opportunistic cancers cannot be prevented by using antibiotics. However, certain types of cancer seem less likely to develop when anti-HIV drugs are used. In women, cervical cancer may be prevented by getting regular Pap tests. When cancer occurs, its treatment depends on the type of cancer (see "Cancers in HIV infection" section below).

All opportunistic conditions can be serious and many are life-threatening. If signs of an opportunistic infection develop, such as fever, weakness, cough, shortness of breath, or pain, it is important to see your doctor quickly for diagnosis and treatment. Many opportunistic infections can be cured, and others can be controlled with drugs. Again, anti-HIV drugs are usually used along with treatments for the illness, to help the immune system and speed up recovery.

Anti-retroviral therapy

The main treatment for HIV at this time uses 3 or more drugs that help block new viruses from forming. Anti-HIV drugs are often called anti-retroviral drugs or ARVs (anti-retrovirals) because HIV is a type of retrovirus.

Combinations of anti-HIV drugs that are very good at stopping HIV growth are sometimes called highly active anti-retroviral therapy (HAART). Stopping or slowing the growth of HIV with these drugs helps improve the quality and length of the person's life.

The best anti-retroviral treatment combination varies with the person, disease stage, whether the person's infection is resistant to any anti-retroviral drugs, and other factors. Study after study has shown that with effective treatment using 3 or more drugs, people live longer and the disease progresses more slowly. However, no combination of drugs available at this time can actually get rid of all the HIV in your body.

When is anti-retroviral treatment started?

Anti-retroviral treatment should be started after you and your doctor discuss the risks and benefits of the drugs you are thinking about taking. The best time to start is not clear-cut, because HIV is an infection that usually progresses slowly.

Disease progression: Most doctors agree that anti-retroviral treatment should begin when:

  • the HIV infection is causing significant symptoms (serious infections, cancers, or physical weakening), regardless of CD4 count and viral load.
  • the CD4 level is below 350, even if there are no symptoms. Some doctors wait until the CD4 level nears 200 before starting the medicines.

People with viral loads over 100,000 are at risk of losing immune function, shown by a quicker drop in CD4 counts. These people may need to see the doctor more often to closely watch CD4 counts so that medicine can be started before the counts go too low. This is especially important as the counts are dropping down near the danger zone, in which the person is at higher risk for serious HIV-related conditions. Since older people are more likely to have these conditions, the need for treatment may be higher for them.

There may be other reasons to begin or delay treatment, and these should be discussed with your doctor. For example, the potential side effects of treatment may make you want to delay it for as long as possible. Or you may want to be treated before your CD4 counts drop to help preserve immune function and further reduce the risk of AIDS-related conditions.

Pregnancy: One very good reason to take anti-HIV drugs is pregnancy. Experts recommend that pregnant women take anti-HIV drugs, whether or not they are at a stage where they would normally be treated for their infection. These drugs are taken every day during pregnancy and delivery to reduce the baby's risk of being infected with HIV. The mother's viral load is watched carefully during pregnancy and kept as low as possible. After the baby is born, the mother may stop the HIV treatment drugs, depending on her HIV stage and situation. However, the baby is treated for a few weeks. The mother is advised not to breast-feed, since she can still pass on the infection in this way.

Kidney disease due to HIV (HIV nephropathy): Experts recommend that anyone who already has kidney problems caused by HIV take anti-HIV drugs to prevent further loss of kidney function. Treatment with anti-HIV drugs also improves survival.

People who are treated for hepatitis B infection: People with the hepatitis B virus (HBV) are often given lamivudine or emtricitabine. These 2 drugs actually started out as anti-HIV drugs, and are still used for treating HIV (see section below, "Antiretroviral drugs used to treat HIV and AIDS"). Doctors later learned that they were good for treating hepatitis B as well, so now the drugs are used for both infections. Unfortunately, if one of these drugs is given to treat HBV in a person who also has HIV, the HIV in the person's body can become resistant to the drug (see "Drug resistance" section below). Any resistance to HIV medicines makes HIV much harder to treat. Because of this, anyone who is going to get one of these HBV drugs should get a full set of HIV treatment drugs at the same time to prevent HIV drug resistance.

Primary HIV infection: For those few people whose infection is found within a few days or weeks after exposure (during primary HIV), doctors are still studying whether treatment at this stage might have long-term benefits by stopping certain types of immune system damage. If you are interested in being treated for HIV during this phase, you might want to think about entering a clinical trial (see the "Clinical trials" section).

Anti-retroviral drugs used to treat HIV and AIDS

More than 20 drugs have been approved to treat HIV infections and AIDS. They fall into 6 classes:

Nucleoside or nucleotide reverse transcriptase inhibitors (NRTIs) work by blocking the enzyme reverse transcriptase, which helps the virus make DNA from its RNA. Drugs in this class include:

  • zidovudine (ZDV or AZT)
  • abacavir (Ziagen®)
  • didanosine (Videx®)
  • emtricitabine (Emtriva®)
  • lamivudine (Epivir®)
  • stavudine (Zerit®)
  • tenofovir (Viread®)
  • zalcitabine (Hivid®)

Non-nucleoside reverse transcriptase inhibitors (NNRTIs) work like the ones listed above, but they are chemically different and act on a different part of the reverse transcriptase molecule. There are 4 drugs in this class at this time:

  • nevirapine (Viramune®)
  • delavirdine (Rescriptor®)
  • efavirenz (Sustiva®)
  • etravirine (Intelence™ or TMC-125)

Protease inhibitors (PIs) work differently from the drugs listed above. HIV produces an enzyme called protease in the late stages of its reproduction. The job of protease is to cut a large viral protein into usable sections as the newly-created viruses move out of the cells. When this protein is blocked by a protease inhibitor, the virus cannot be assembled properly. Protease inhibitors include:

  • atazanavir (Reyataz®)
  • indinavir (Crixivan®)
  • nelfinavir (Viracept®)
  • ritonavir (Norvir®)
  • saquinavir (Fortovase®)
  • lopinavir (combined with ritonavir and called Kaletra® – see information below on boosting)
  • fosamprenavir (Lexiva®)
  • tipranavir (Aptivus®)
  • darunavir (Prezista®, which must be taken with ritonavir – see boosting information, below)

Ritonavir has a special use as a protease-inhibitor booster. It was approved as an HIV treatment, and is used in standard doses as part of 3-drug combination treatments for HIV. Along with helping stop the virus, ritonavir was observed to keep certain other protease inhibitors and other drugs in the body longer.

Although ritonavir is still given in standard doses as a protease inhibitor, it is also used in smaller doses along with other protease inhibitors to take advantage of this side effect. This practice is called boosting a protease inhibitor, because it helps keep the drug levels in the body higher and often allows the drug to be given less often. When ritonavir is used solely as a booster, it is given in doses that are not high enough to affect the virus, but just enough to affect the level of the other drug. In this case, it is not being used as an anti-HIV drug, but only as a booster for one of the other drugs. It is important to know that even a small dose of ritonavir can also raise the levels of many other drugs, not just HIV treatment drugs. Anyone taking any dose of ritonavir must always find out about dangerous interactions before starting any new drug.

Entry inhibitors (including fusion inhibitors) work by blocking the virus from entering the host cell. One of the approved drugs, enfuvirtide (Fuzeon®) is called a fusion inhibitor, and must be given by injection. The newer drug in this category is called maraviroc (Selzentry™). It helps to keep HIV out of individual CD4 cells by blocking the protein CCR5. This drug can only be used in patients with a strain of HIV that uses the protein CCR5 as its "door" into the CD4 cell. Before starting this drug, a person must be tested to be sure that the strain of HIV they have is the type this drug can stop.

Integrase inhibitors work by keeping the virus from putting its DNA into the host cell. This keeps the virus from being able to take over the cell to make more viruses. The only drug in this class is raltegravir (Isentress™).

Combination drugs are fixed-dose combinations of the above drugs that help to reduce the number of pills a person has to take. Some examples include:

  • Combivir® - zidovudine and lamivudine
  • Trizivir® - zidovudine, lamivudine, and abacavir
  • Epzicom® - abacavir and lamivudine
  • Truvada® - tenofovir and emtricitabine
  • Atripla® - efavirenz, emtricitabine, and tenofovir

Atripla is the first combination formula that comes in a single pill to be taken once a day. Although not everyone can take this combination, for those who can, it is a major improvement over taking several pills 3 or 4 times a day.

Treatment effectiveness

The success of any antiretroviral regimen is measured by checking the viral load a few weeks after the drugs are started, and then checking the viral load and CD4 count every 3 to 4 months as the drugs are continued. The CD4 count normally goes higher as the viral load goes down.

The goal of treatment is to get the viral load down so that the lab test cannot find any trace of virus in the blood (this is called an undetectable level). Different tests have different cutoffs for detection.

It is important to know that an undetectable virus load does not mean that there is no HIV in the person's blood, only that the test was not able to detect it. Undetectable virus levels do not mean that the person cannot infect others with HIV. Even with undetectable virus loads in the blood, it is still necessary to use safer sex practices and other precautions to avoid passing the virus on to others.

If the viral load cannot be kept down to undetectable levels with the first drug combination, others are usually tried. If no combination gets the viral load down to undetectable levels, doctors usually keep trying until they find a drug combination that will help keep it as low as possible. In such difficult cases, this may mean using more than 3 drugs.

Of the anti-retroviral drugs available today, many are used only after the preferred drugs have failed. Because researchers are still comparing treatments and new drugs are still being tested, the drugs and combinations used for HIV treatment continue to change as more research is completed.

HIV treatment issues

Drug resistance: Treating HIV infection is difficult, in part because the virus can change its proteins and become drug resistant. This means that the virus learns to multiply even when the anti-retroviral drugs are in your body. This is one reason that anti-retroviral drugs are never used alone or even in pairs – if HIV can grow even a little bit while a drug is in your system, those viruses often become more and more resistant to that drug. It usually takes the full effect of 3 drugs to stop HIV growth, so all of the anti-retroviral drugs must be taken on time in order to work properly. HIV can quickly become resistant to anti-retroviral drugs if they are not taken as prescribed.

Taking anti-HIV drugs exactly as prescribed can be hard for many people. Some drugs are taken 3 times a day, others once a day. Some don't work if they are taken with food, and others work better if they are taken with a meal. This can be confusing and complicated. It may take some time for a person to be ready for this kind of commitment. If you are not able to keep to a strict schedule, you need to discuss this with your doctor. You may be able to work out an easier regimen. Many doctors now try to start with combinations of drugs that can be taken once or twice a day. However, drug resistance testing may show that your options for effective treatment drugs are limited. If the first drug combination fails, or if you cannot take it, it becomes harder to find a second or third combination that works well. After a few drugs have failed, it may take more elaborate combinations of 4 or 5 drugs to try and keep the virus from growing.

Even when taken exactly as prescribed, people are likely to develop drug-resistant virus after years on the drugs. If the virus load begins to increase while the patient is taking anti-retroviral drugs correctly, a drug resistance test is usually done to learn which drug or drugs the virus is resistant to. Unfortunately, many of the HIV drugs are similar, and resistance to one drug may mean resistance to more drugs in the same class. This limits the number of drug combinations that a person might expect to use after one or more combinations fail. Some people have HIV that has already become resistant to all the drugs that are available today. It is also possible for a person with drug-resistant virus to transmit that virus to others. This means that an increasing number of people who get HIV find that they already have drug-resistant virus, even before they have taken any drugs to treat HIV.

Drug interactions: Another challenge of anti-retroviral drugs, especially the protease inhibitors, is that they can interact with other drugs. This means that one or more drugs might not work, or that one might build up to toxic levels in the body. For example, some anti-retroviral drugs interact with certain antibiotics, cholesterol-lowering drugs, anti-seizure drugs, birth control pills, erectile drugs, or even other anti-retrovirals. Each time a new drug is prescribed, your doctor and pharmacist should review all your drugs and supplements to be sure that no harmful interactions are likely. This can complicate treatment of many conditions.

As noted above, ritonavir interacts with many other drugs in ways that can be dangerous. However, some treatment regimens exploit this property of ritonavir by using fewer doses of certain other protease inhibitors to achieve the same effect. In cases such as this one, doses can be adjusted, but there are a few drugs that are simply not safe to use with some HIV drugs. This is one of the reasons it is important to keep a list of all your drugs, along with the dose and how often you take them, with you at all times. It also means that if you are taking one of these interacting drugs and stop taking it, you may need to have other drug doses adjusted back to the usual levels.

Side effects: Like all drugs, anti-retroviral drugs can have side effects. Short-term side effects show up within a few days or weeks, depending on the drug. They can range from nausea, vomiting, diarrhea, headaches, and rashes, to severe allergic reactions. Most of these effects only happen to a few people who take the drugs. Each drug has specific side effects, which need to be discussed with your doctor. But some side effects are typical of each class.

The NRTIs can cause acidosis of the blood, which is a serious chemical imbalance, in a few people. Acidosis can make you feel very weak and short of breath. This very rarely occurs, but if it happens, you need to see a doctor right away, preferably in an emergency room. A blood test can show if you have acidosis. NRTIs can also cause fatty changes in the liver, usually after 6 months or more. They can also cause lipodystrophy, a condition in which body fat can build up on the chest and abdomen and be lost from the arms and legs. These drugs lower blood counts and can cause fatigue, nausea, anemia, headaches, and other symptoms in some people. AZT causes the most problems with blood counts, although only in some patients.

Abacavir is also known for causing a type of allergic reaction that damages organs in certain people. Now, doctors can test for this reaction before this drug is even started. However, most side effects can be found only after a person starts taking the drug.

The NNRTIs can cause rashes and allergic reactions. They can also lead to liver damage, which is usually found through blood tests and is rarely a serious problem. The NNRTIs can also affect mood, thinking, and sleep patterns. One drug in this class, efavirenz, can cause birth defects if it is taken by pregnant women.

The PIs can also cause body fat to redistribute (lipodystrophy). Over the long term, they can raise blood levels of cholesterol and triglycerides and increase risk of heart attacks. They can raise blood sugar and even cause diabetes in some people. Cholesterol and blood sugar levels are checked regularly while a patient is on these drugs, and some people may require treatment if there are problems. It is important to reduce the risk of heart problems by avoiding tobacco, eating healthy, and staying active.

Entry inhibitors can cause serious rashes and allergic reactions with fevers, chills, trouble breathing, and faintness or dizziness. Maraviroc can cause liver damage in some people, with symptoms like jaundice (yellowing of the skin or eyes). Because enfuvirtide is injected, people can develop irritations or infections at the injection site.

Integrase inhibitors can cause milder symptoms such as nausea, headache, fever, and diarrhea. A few people develop a serious problem that shows up with muscle pain, weakness, and dark colored urine.

As part of follow-up with patients on HIV drugs, most doctors check labs often and watch for signs of diabetes, hyperlipidemia (high cholesterol and triglycerides), fat redistribution (lipodystrophy), liver damage, low blood counts, and other side effects that may worsen the longer the drugs are given. Some drugs cause very specific side effects that may go on even after the drug that caused them is stopped. In rare cases, side effects may be serious enough that the person may need some time in the hospital. Talk with your doctor or nurse about what you can do to reduce your risk of side effects. Find out which side effects need to be reported to the doctor right away and what to do if you should have these problems after office hours or on weekends.

Cost: Combination treatment can be costly (around $15,000 per person per year for the drugs alone, not including labs and doctor visits). It is important to talk with your doctor about what you can afford or what insurance will pay, as well as how likely you are to stick to the planned drug program. HIV drugs must be taken exactly as directed for them to work.

Guiding principles of treatment

In 1997, the Office of AIDS Research of the National Institutes of Health (NIH) brought together a panel of experts to discuss the advances in basic HIV research, treatment research, and testing in order to give the best information to doctors and patients. The final report presented the following principles that have guided treatment for a decade. They are summarized here because they offer some of the most important information about HIV and its treatment:

  • HIV infection is always harmful, and true long-term survival without serious loss of immune function is unusual. When HIV continues to reproduce, it damages the immune system and leads to AIDS.
  • Regular, periodic viral load tests and CD4 lymphocyte counts are necessary to find out when to start or change anti-retroviral therapy and to learn the risk of disease progression.
  • The time to start HIV treatment should be based on risk of disease progression and amount of immune deficiency, and these vary with individual patients.
  • The goal of treatment is to keep HIV from growing, so that it stays below levels that can be detected by viral load tests.
  • The anti-retroviral drugs used in combination must be carefully chosen and given together.
  • Each anti-retroviral drug in a combination treatment regimen should always be used according to the most effective schedules and dosages.
  • Any change in a person's anti-retroviral treatment reduces future treatment options.
  • Women should receive effective anti-retroviral therapy even when pregnant.
  • The principles of anti-retroviral therapy presented above apply to both HIV-positive children and adults, although the treatment of HIV-positive children involves unique considerations.
  • Persons with acute (primary) HIV infection may also benefit from combination anti-retroviral therapy to decrease the virus load to undetectable levels.
  • All HIV-infected persons, including those with viral loads below detectable levels, should be considered infectious and should avoid sexual and drug-use behaviors linked to giving or getting HIV and other infections.

Treatment follow-up

Because of side effects, many people would like to sometimes stop therapy and take a short break. Most doctors think this is risky, and will not recommend it until clinical trials show this can be done safely. It is important that people getting treatment stick closely to their regimen (drug schedule). Missing doses of drugs allows the virus to grow back very quickly, and increases the risk of drug resistance. Stopping one anti-HIV drug while continuing to take the others may allow the virus to quickly develop resistance to the remaining drugs. (See the information on "Drug resistance" above.) If you are having problems with the regimen, talk to your doctors and find out if an easier one can be worked out.

Your doctor will check your blood counts, your CD4 counts, measure the viral load in your blood, and generally watch your health while you are on anti-retroviral drugs. At some point, your viral load may begin to creep up after it has been down for a while. This can happen quickly if you miss doses. It can also mean the virus is becoming resistant to one or more of the drugs you are on, and your doctor may test your blood to see which drugs will be most effective. It is not unusual for HIV to develop resistance, especially after a couple of years, and most people will need to change drug regimens at some point.