Esophagus Cancer

What Is Cancer of the Esophagus?

The esophagus is a muscular tube that connects the mouth to the stomach. It carries food and liquids to the stomach. It is about 10-13 inches long. At its smallest point, it is a little less than
one inch wide.

The wall of the esophagus has several layers. Cancer of the esophagus starts from the inner layer and grows outward.

At the top of the esophagus is a special muscle that relaxes to let food or liquid enter. This muscle is called a sphincter. The lower part of the esophagus connects to the stomach. Another muscle here opens to allow food to enter the stomach. This muscle also keeps stomach acid and juices out of the esophagus. When stomach juices escape into the esophagus, we feel heartburn. The medical term for heartburn is reflux.

Long-term reflux of stomach acid into the esophagus sets up a special problem. It can change the cells in the lower end of the esophagus. They become more like the cells that line the stomach. These changed cells produce a condition called Barrett esophagus. The altered cells can change into cancer, so they should be closely watched by a doctor.

There are 2 main types of cancer of the esophagus. One type grows in the cells that form the top layer of the lining of the esophagus. These are called squamous cells, and cancer that starts there is known as squamous cell carcinoma. Squamous cell cancer can grow anywhere along the length of the esophagus. It accounts for about half of all cancers of the esophagus.

The other type usually starts near the opening to the stomach. It is called adenocarcinoma. This type of cancer cannot start unless squamous cells have been changed by acid reflux.

What Causes Cancer of the Esophagus?

While we don't know the exact cause of esophageal cancer, we do know some of the risk factors that make this cancer more likely. A risk factor is something that increases a person's chance of getting cancer. Some risk factors, such as smoking, can be controlled. Others, like a person's age or race, can't be changed.

Risk Factors for Cancer of the Esophagus

Age: The risk of this cancer goes up with age. It is rarely found in people under 40.

Sex: Men are 3 times more likely to get this cancer than women.

Race: African Americans are 50% more likely to develop cancer of the esophagus than whites.

Barrett esophagus: This occurs because of long-term reflux of fluid from the stomach into the lower esophagus. Some people feel heartburn from this reflux and others do not. Over time this reflux can change the cells at the end of the esophagus. This raises the risk of adenocarcinoma of the esophagus. But not everyone with Barrett esophagus will get cancer of the esophagus.

Heartburn: Long-standing heartburn, also called reflux (or GERD: gastroesophageal reflux disease), increases the risk of this cancer even if it hasn�t progressed to Barrett esophagus.

Tobacco: Using any form of tobacco raises the risk of this cancer. The longer a person uses tobacco, the greater the risk. More than half of all squamous cell esophageal cancer is linked to smoking.

Alcohol: Long-term heavy drinking is a major risk factor for cancer of the esophagus. For people who both smoke and drink, the risk is further increased.

Overweight: The risk of this cancer is higher for people who are overweight or obese.

Diet: Diets that don�t include enough fruits or vegetables and certain minerals and vitamins can raise the risk of this cancer. Overeating, which leads to being overweight, also raises the risk of this cancer.

Very hot liquids: Drinking lots of very hot liquids might increase the risk of this cancer.

Chemicals: Working with a chemical used in dry cleaning may lead to a greater risk of this cancer. Dry cleaning workers have a higher rate of cancer of the esophagus. Also, breathing in many other chemical fumes may also increase the risk.

Lye: Lye is found in strong cleaners like drain cleaners. It can burn and destroy cells. If a child accidentally drinks one of these cleaning liquids, the lining of the esophagus will scar. A child who has swallowed lye has a higher risk of squamous cell cancer as an adult.

Achalasia: In this disease, the muscle at the bottom of the esophagus does not open to release food into the stomach. So the lower end of the esophagus expands. Food collects there instead of moving into the stomach. This raises the risk for squamous cell cancer.

Tylosis: This is a rare, inherited disease. Extra skin grows on the palms of the hands and soles of the feet. People with tylosis are at a very high risk for esophageal cancer. They should be seen by a doctor regularly.

Esophageal webs: These are abnormal pieces of tissue that extend into the esophagus. They can make it hard to swallow. People who have these usually have other symptoms as well. They can have problems with the tongue, fingernails, spleen, and other organs. About 1 in 10 people with this problem will get cancer of the esophagus.

How Is Cancer of the Esophagus Found?

People with Barrett esophagus and others at high risk should have exams to look for cancer of the esophagus. The doctor might recommend surgery (or other methods) if certain abnormal cells (dysplasia) are found.

In most cases, this type of cancer is found because of the symptoms it causes. But often these symptoms don't appear until the cancer is advanced, making a cure less likely. If the cancer is found early, it is often a result of tests done for other reasons.

Below are the most common symptoms of this type of cancer:

Trouble with swallowing (dysphagia: dis-FAY-jee-uh): This is the most common symptom of cancer of the esophagus. It means that you feel as if food is lodged in the chest. By this time, if cancer is present it has grown to fill about half the opening of the esophagus. Solid foods like bread and meat often get stuck. People with dysphagia often switch to softer foods or even liquids to help with swallowing. To help the food go down, the body makes more saliva. This causes some people to bring up lots of thick mucus or saliva.

Pain: Rarely, pain in the mid-chest, or a feeling of pressure or burning, can be a sign of cancer. But these symptoms can also be caused by something else, such as heartburn. Pain while swallowing is usually a late sign of a large cancer.

Weight loss: About half of people with esophageal cancer lose weight without trying. This is because they are not getting enough food since they have trouble swallowing. Also, they may find they have less appetite.

Other symptoms: Hoarseness, hiccups, pneumonia, and high calcium levels are usually signs of more advanced cancer. Of course, these symptoms can be caused by other diseases as well.

How Is Cancer of the Esophagus 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 to you about a treatment plan. There is a lot for you to think about when choosing the best way to treat or manage your cancer. There may be more than one treatment to choose from. You may feel that you need to make a decision quickly. But give yourself time to absorb the information you have learned. Talk to your doctor. Look at the list of questions at the end of this piece to get some ideas. Then add your own.

You may want to get a second opinion. A second opinion can provide more information and help you feel good about the treatment you choose. Some insurance companies require you to get a second opinion before they will agree to pay for treatments.

Surgery, chemotherapy, and radiation are used to treat early cancer of the esophagus. There are also treatments to help relieve pain and help with symptoms.

The best choice for you will depend on the stage of the cancer as well as your general health. Each kind of treatment might have side effects. Your cancer care team will be glad to discuss the side effects with you.

Surgery

How much surgery is done depends on the stage of the cancer. Surgery can also be used along with other treatments such as chemotherapy and radiation treatment.

There are 2 common types of operations for this cancer. In one, esophagectomy (ee-sof-uh-JEK-tuh-me), the part of the esophagus with cancer and nearby lymph nodes are removed. The esophagus is attached either to the stomach or the surgeon may replace the removed part of the esophagus with a piece of the small or large intestine.

The other surgery, esophagogastrectomy (ee-sof-uh-go-gas-TREK-tuh-me), is done to remove part of the lower esophagus, nearby lymph nodes, and the upper part of the stomach. The esophagus is again connected to the remaining part of the stomach.

While surgery can cure some patients whose cancer has not spread beyond the esophagus, often these cancers are not found early enough. So it�s important to know the goal of surgery: is it to try to cure the cancer or to ease symptoms?

Both of these operations are complex. Some surgeons are able to do the operation using a laparoscopic approach. This means that small cuts are made through which the doctor uses a tiny instrument something like a telescope to look inside the body. The surgery itself is done through even smaller incisions.

Surgeons who do this surgery must be quite expert. You should feel free to ask your surgeon about his or her experience with these operations and what percent were successful. The success rate is greater when the surgery is done in a hospital where it is done more often.

Most people stay in the hospital for 2 weeks after surgery. And there can be risks and side effects. For example, after the operation the stomach may empty very slowly, causing nausea and vomiting. The place where the esophagus connects to the stomach can become more narrow, making it hard for the person to swallow. Also, acid from the stomach can enter the esophagus causing heartburn. Anyone who has problems with side effects should talk with their doctor or nurse as there are often ways to help.

Some complications from surgery can be very serious, even fatal. It is important to have a surgeon with experience in a hospital where these operations are done more often. Don�t be afraid to ask the surgeon about his or her experience and about the survival rates at the hospital.

Radiation Therapy

Radiation therapy is treatment with high energy rays (such as x-rays) to kill or shrink cancer cells. External radiation uses a beam from outside the body. This is the kind most often used for cancer of the esophagus. For internal or implant radiation, radioactive �seeds� are placed directly inside the body near the cancer.

Radiation therapy by itself will not cure esophageal cancer. Often it is combined with surgery and/or chemotherapy. It is also used to relieve problems with swallowing, pain, or other symptoms of this cancer.

Side effects of radiation treatment may include skin problems, upset stomach, diarrhea, and fatigue. Often these side effects go away when treatment ends. Radiation to the chest may cause lung damage and lead to trouble breathing and shortness of breath. If you have these or other side effects, talk with your doctor since there are often ways to relieve them.

Chemotherapy

Chemotherapy 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.

Chemotherapy alone cannot cure cancer of the esophagus unless radiation treatment (and in some cases surgery) are also used. Chemotherapy is used in 3 ways:

  • It can be used to ease the symptoms of advanced cancer.
  • It can be given along with radiation to shrink the cancer.
  • It can be used before surgery to shrink a tumor. This use is still being studied.

Chemotherapy can have some side effects. These side effects will depend on the type of drugs given, the amount taken, and how long treatment lasts. The most common side effects can include:

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

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

PDT (photodynamic therapy): This method may be used when the cancer has been found very early or has come back after other treatment. First, a harmless chemical is injected into the bloodstream. It collects in the tumor for a few days. Then a special type of laser light is focused on the cancer through an endoscope. The light changes the chemical into a new chemical that can kill cancer cells.

PDT is useful because it can kill cancer cells with very little harm to normal cells. But because the light must be used, it can reach only cancers near the surface of the esophagus. It doesn�t work for cancers that have spread deeper or into other organs.

Side effects of PDT include redness or discoloration of the skin and sensitivity to the sun or other light sources. Because of this, people having this treatment may be told to stay indoors for 6 weeks.

At this time, the main use of PDT is to relieve symptoms of advanced cancer that are blocking the esophagus. It is also being used to treat Barrett esophagus and very early cancers found in Barrett esophagus. Researchers are looking at the use of PDT in comparison to other treatments such as surgery or the use of lasers.

Survival Rates by Stage (from the National Cancer Data Base; based on 11,154 patients diagnosed in 1998)

Because this cancer is usually found at an advanced stage, many people will die of the disease. But survival rates have been getting better. 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.

The 5-year survival rate is the percentage of patients who are alive 5 years after diagnosis (leaving out those who die of other causes). Of course, patients might live more than 5 years after diagnosis.

Stage 5-year relative survival rate
0 52%
I 41%
II 26%
III 13%
IV 3%

Endometrial Cancer

What Is Endometrial Cancer?

Endometrial cancer is a cancer that starts in the inner lining of the womb (uterus). This lining is called the endometrium. The pictures below show where the uterus is found and then a closer look at the uterus.

diagram of the ovaries

diagram of the uterus

The uterus is a hollow organ, about the size and shape of a medium-sized pear. It has 2 main parts. The lower part, which extends into the vagina, is called the cervix. The upper part is the body of the uterus, also known as the corpus. The body of the uterus has 2 layers. The inner layer is called the endometrium.

During a woman's menstrual cycle this inner layer changes. In the early part of the cycle it gets thicker in case the woman becomes pregnant. If she does not become pregnant, the tissue is shed from the uterus and becomes the menstrual flow. This cycle repeats throughout a woman's life until change of life (menopause).

Types of cancers of the uterus and endometrium

Nearly all cancers of the uterus start in the endometrium. They are called endometrial carcinomas. Cancers can also start in the muscle layer of the uterus. These cancers belong to the group of cancers called sarcomas.

Carcinomas

Most carcinomas are cancers that start in the cells that form glands in the lining of the uterus. They are called adenocarcinomas. Among these there are 2 types. In the first and most common type, the cancer cells look a lot like normal cells. This is called endometrioid adenocarcinoma. This type can be less likely to spread, which makes it less dangerous. The other type of endometrial cancer is less common and more likely to grow and spread quickly.

Uterine sarcomas

Less common uterine cancers that do not come from glandular tissue of the endometrium are called uterine sarcomas. These can involve the endometrium. These types of cancer are not covered here because their treatment and outlook for survival are different from the most common cancers of the endometrium. If you would like to know more about this type of cancer you can get our document called Uterine Sarcoma.

Cervical cancers

Cancers of the cervix are different from cancers of the body of the uterus and are described in our document, Cervical Cancer.

What Causes Endometrial Cancer?


We do not yet know what causes most cases of endometrial cancer. But we do know that certain risk factors are linked to this disease. A risk factor is anything that changes a person's chance of getting a disease such as cancer. Different cancers have different risk factors. For example, being in strong sunlight without protection is a risk factor for skin cancer. Smoking is a risk factor for many cancers. But risk factors don't tell us everything. Someone can have several risk factors and still not get a disease. Also, not having any risk factors doesn't mean that you won't get the disease.

Risk factors for endometrial cancer

Hormone levels

A woman's hormone balance plays a part in most endometrial cancers. Many of the risk factors for endometrial cancer affect estrogen levels. Before change of life, the ovaries are the main source of the 2 main types of female hormones -- estrogen and progesterone. The balance between these hormones changes during a woman's menstrual cycle each month. A shift in the balance of these 2 hormones toward more estrogen increases a woman's risk for getting endometrial cancer.

After change of life, the ovaries stop making these hormones, but a small amount of estrogen is still made in fat tissue. Female hormones can also be taken as birth control pills to prevent pregnancy and as hormone therapy to treat symptoms of menopause.

Estrogen therapy: Using estrogen to treat symptoms of change of life is known as estrogen therapy or menopausal hormone therapy. Estrogen treatment can reduce hot flashes, improve vaginal dryness, and help prevent the weakening of the bones (osteoporosis) that can happen with menopause. But the use of estrogen alone increases a woman's risk of getting endometrial cancer. Studies show that giving progesterone-type drugs along with the estrogens helps lower this risk. But studies also show that giving this combination of the hormones increases a woman's chance of getting breast cancer and blood clots.

It is important to discuss the pros and cons of estrogen therapy with your doctor. If you choose to take it, you should use the lowest dose that is needed for the shortest period of time. You should also have follow-up exams for cancer at least every year. Let your doctor know right away if you have any vaginal bleeding or discharge that isn't normal.

Birth control pills: Using birth control pills lowers the risk of endometrial cancer. The risk is lowest in women who take the pill for a long time. And this protection continues for at least 10 years after a woman stops taking this form of birth control. But you need to look at all of the pros and cons when choosing a birth control method -- endometrial cancer risk is only one factor to think about. It's a good idea to talk to your doctor about the different methods of birth control to find the one that is best for you.

Total number of menstrual cycles (periods): Having more periods during a woman's lifetime raises her risk of endometrial cancer. Starting periods before age 12 or going through change of life late raises the risk. Starting periods early is less a risk factor for women with early change of life. Likewise, late change of life may not lead to a higher risk in women whose periods began later in their teens.

Pregnancy: During pregnancy, the hormonal balance shifts toward more progesterone. So having many pregnancies reduces endometrial cancer risk. Women who have not been pregnant have a higher risk.

Obesity (being very overweight): Most of a woman's estrogen is made by her ovaries, but fat tissue can change some other hormones into estrogens. Having more fat tissue can increase a woman's estrogen levels and, as a result, increase her endometrial cancer risk.

Tamoxifen: Tamoxifen is a drug that is used to treat women with breast cancer. It is also used to reduce the risk in women who are at a high risk of getting breast cancer. The drug acts like estrogen in the uterus. It can cause the uterine lining to grow and increase the risk of endometrial cancer in women who take this drug.

The risk of getting endometrial cancer in women taking tamoxifen is fairly small (about 1 in 500). It must be balanced against the value of this drug in treating breast cancer and reducing the chances of the woman getting cancer in the other breast. This is something women may want to talk about with their doctors. If you decide to take tamoxifen, you should have yearly pelvic exams. You should also be sure to tell your doctor if you have any endometrial cancer symptoms, such as discharge or bleeding that isn't normal.

Ovarian tumors: Certain ovarian tumors make estrogen. Women who have these tumors have higher than normal estrogen levels and lower levels of progesterone. The increase in estrogen compared to progesterone can increase a woman's chance of getting endometrial cancer.

Polycystic ovarian syndrome: Women with polycystic ovarian syndrome (PCOS) have hormone levels that are not normal, such as higher estrogen levels and lower levels of progesterone. The increase in estrogen compared to progesterone can increase a woman's chance of getting endometrial cancer.

Age

The risk of endometrial cancer goes up as a woman gets older.

A diet high in animal fat

A high-fat diet can increase the risk of several cancers, including endometrial cancer. Because fatty foods are also high-calorie foods, a high-fat diet can lead to obesity, which is an endometrial cancer risk factor. Some doctors think that fatty foods may also have a direct effect on estrogen levels, which can also increase risk.

Diabetes

Diabetes is more common in people who are overweight. This could be why diabetes is a risk factor for endometrial cancer. But some studies suggest that diabetes by itself could be a risk factor.

Family history

This cancer appears to run in some families who also tend to get a certain type of colon cancer. A small number of endometrial cancers may be due to this inherited factor. Women who have had several family members with colon cancer or endometrial cancer might think about having genetic counseling and testing. This kind of testing can help show if you (or members of your family) are at high risk. If you are, your doctor may suggest a hysterectomy once you are through having your children. Your doctor may also recommend endometrial sampling (biopsy) every year for women age 35 or older.

Breast or ovarian cancer

Women who have had breast cancer or ovarian cancer may have a higher risk of getting endometrial cancer. Some of the risk factors for breast and ovarian cancer also increase endometrial cancer risk.

Earlier pelvic radiation therapy

Radiation used to treat some other cancers can damage the DNA of cells. This could increase the risk of getting a second type of cancer, such as endometrial cancer.

Endometrial hyperplasia

Endometrial hyperplasia is an increased growth of the endometrium. The most common type has a very small risk of becoming cancer. It may go away on its own or after treatment with hormones. If the hyperplasia is called "atypical," it has a higher chance of becoming a cancer.

It is important to keep in mind that although these factors may increase a woman's risk for getting endometrial cancer, they do not always cause the disease. Many women with one or more of these risk factors never get endometrial cancer, and some women with endometrial cancer do not have any of these risk factors.

How Is Endometrial Cancer Found?

Most women are diagnosed because they have symptoms. Watching for any signs and symptoms of this cancer and telling your doctor about them right away allows the cancer to be found at an early stage. Finding it early improves the chances that it will be treated with success. But sometimes this cancer can reach an advanced stage before it causes any symptoms.

Early detection tests

Early detection refers to testing to find a disease such as cancer in people who do not have symptoms of that disease.

Women at average endometrial cancer risk

Women should talk to their doctors about getting regular pelvic exams, including Pap tests. Although the Pap test can find some female cancers early, most cases of endometrial cancer are not found by this test. But the Pap test is very good at finding early cancer of the cervix (the lower part of the uterus).

After menopause you should tell your doctor if you have any discharge or bleeding that is not normal. This could be a sign of endometrial cancer.

Women who have a higher risk of endometrial cancer

Women at high risk for this cancer should see their doctor whenever they have any vaginal bleeding that is not normal. This includes women who:

  • are older
  • had late menopause
  • never had children
  • are unable to get pregnant (infertile)
  • are obese
  • have diabetes
  • have high blood pressure
  • are using estrogen treatment
  • are taking tamoxifen therapy

Women who have (or are at risk for) a certain type of colon cancer (hereditary nonpolyposis colon cancer, or HNPCC), should have yearly testing with an endometrial biopsy beginning at age 35. Another option would be for the woman to have a hysterectomy once she is finished having children.

Signs and symptoms of endometrial cancer

Unusual bleeding, spotting, or other discharge

If you have gone through change of life (menopause) it is very important to tell your doctor about any bleeding or spotting that is not normal. About 9 out of 10 women with endometrial cancer have some type of abnormal vaginal bleeding, but some have discharge that does not look like blood. Abnormal discharge also can be caused by something other than cancer.

Pelvic pain or a mass and weight loss

These symptoms usually happen in the later stages of the disease. Still, you should see the doctor right away because a delay in getting treatment can allow the cancer to get worse. This lowers the chance for successful treatment.

What will happen next?

History and physical exam

The doctor will ask about your symptoms, risk factors, and family medical history. The doctor will also do a physical and a pelvic exam.

Seeing a specialist

If the doctor thinks you might have endometrial cancer, you should see a gynecologist--a doctor with special training in finding and treating diseases of the female reproductive system.

Getting a sample of endometrial tissue

To find out whether the problem is endometrial hyperplasia or endometrial cancer, the doctor must remove some tissue so that it can be looked at under the microscope. Tissue can be taken out by doing an endometrial biopsy or by a D & C (this stands for dilation and curettage). These are described below.

Endometrial biopsy

This kind of biopsy can be done in a doctor's office. A very thin flexible tube is placed into the uterus through the cervix. Then suction is used to remove a small amount of endometrium. The suction usually takes less than a minute. The discomfort is much thing like menstrual cramps and can be helped by taking a drug like ibuprofen before the test.

Hysteroscopy

This is a way that doctors can look inside the uterus. The doctor puts a tiny telescope into the uterus through the cervix. The uterus is then filled with salt water (saline). This lets the doctor see and take a sample of anything that might be causing a problem, such as a cancer or a polyp. You stay awake for this, and the biopsy is done after the area is numbed with medicine.

Dilation and curettage (D & C)

If the biopsy sample doesn't get enough tissue, or if the doctor can't tell for sure whether it is cancer, a D & C must be done. To do this, the cervix is opened (dilated) and a special instrument is used to scrape tissue from inside the uterus. The test takes about an hour and you may need medicine to make you sleep (general anesthesia). D & C is most often done in an outpatient surgery area of a clinic or hospital. Most women have little pain after this procedure.

Testing the tissue

Tissue that has been removed is looked at under a microscope to see whether there are cancer cells in it. If cancer is found, the cells will be studied to learn more about the cancer. The lab report will give these details.

The lab will also assign a grade to the cancer. If most of the cancer cells look like normal tissue, it’s given a grade 1. If most of the cells look very different from normal cells, it's given a grade of 3. Grade 2 tumors fall somewhere in between. The grade is important because women with lower grade cancers are less likely to have advanced disease or to have the cancer come back after treatment.

Imaging tests for endometrial cancer

Ultrasound

Ultrasound is the use of sound waves to take pictures of the inside of the body. For this test, a probe is placed into the vagina. It gives off sound waves that echo off the tissue of the pelvic organs to create a picture on a video screen. This test can be used to see if there is a tumor. It could also show whether the tumor is growing into the outer muscle layer of the uterus. Salt water (saline) might be put into the uterus before the test to give a clearer picture.

Cystoscopy and proctoscopy

If a woman has signs that suggest the cancer may have spread, the doctor can use a lighted tube to look at the inside of the bladder or rectum. Small pieces of tissue can be removed to be looked at under a microscope.

CT scan

This is a special type of x-ray that creates detailed pictures of the inside of the body. CT scans are rarely used to find endometrial cancer. But they may be helpful if it looks as if the cancer has come back or has spread into the liver or other organs. CT scans can also be used to guide a biopsy needle into the area that could be cancer.

CT scans take longer than regular x-rays. You will need to lie still on a table while the scans are done. You may also have an IV (intravenous) line through which a contrast "dye" is injected. Some people are allergic to the dye and get hives or, rarely, problems like trouble breathing and low blood pressure. Be sure to tell the doctor if you have ever had a problem from any dye used for x-rays. You may also be asked to drink 1 to 2 pints of a liquid that helps outline the intestine so that it is not mistaken for tumors.

MRI scan (magnetic resonance imaging)

MRI scans use radio waves and strong magnets instead of x-rays. MRI scans are helpful in looking at the brain and spinal cord. They take longer than CT scans, and you may have to be placed inside a tube-like machine. This can be upsetting for some people. Sometimes newer "open MRI" machines are used. The machine makes thumping or buzzing noises that you may find disturbing. Many places will give you headphones with music to block this out. A contrast dye might be used, just as with CT scans.

PET scan (positron emission tomography)

In this test, a type of radioactive sugar is given to look for cancer cells. The cancer cells take in large amounts of the sugar. A special camera can then detect where it goes in the body. PET is sometimes useful in finding small collections of cancer cells. But PET is not often used for endometrial cancer.

Chest x-ray

This can show if the cancer has spread to the lungs. It may also be used to look for serious lung or heart problems.

IVP (intravenous pyelogram)

An IVP may be done if the doctor thinks the cancer might have spread to the urinary tract or nearby tissues. An IVP is an x-ray that outlines the urinary system. But CT scans are used more often than IVP.

Blood tests

Complete blood count (CBC)

This test measures the different cells in the blood, such as the red blood cells, white cells, and platelets. Many times women who have lost blood from the uterus will have low red blood cell counts. This is called anemia.

CA 125 blood test

CA 125 is a substance that many endometrial and ovarian cancers release into the bloodstream. Very high blood CA 125 levels are a sign that the cancer has likely spread beyond the uterus. If CA 125 levels are high before surgery, some doctors will track this number to find out how well the treatment is working. The levels will go down after surgery if treatment is killing the cancer cells. CA 125 levels may also be watched to see if the cancer has come back after treatment is done.

How Is Endometrial 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 going over your test results, your doctor will recommend one or more treatment options. Don't feel rushed about making a decision. If there is anything you do not understand, ask to have it explained again. The choice of treatment mostly depends on the type of cancer and stage of the disease when it is found. Other factors that could play a part might include your age, your overall health, whether you plan to have children, and other personal matters. Be sure you understand all the risks and side effects of the different treatments before making a decision.

You may want to get a second opinion. This can give you more information and help you feel more certain about the treatment plan you choose. Some insurance companies say you must get a second opinion before they will pay for some treatments, but most of the time a second opinion is not needed for routine cancer treatments.

There are 4 basic types of treatment for women with endometrial cancer: surgery, radiation therapy, hormone therapy, and chemotherapy (chemo). Surgery is the main treatment for most women with endometrial cancer. But sometimes one or more of these treatments is combined.

Surgery

Hysterectomy

The main treatment for endometrial cancer is an operation to remove the uterus and cervix. This is called a hysterectomy. Most often, the ovaries and fallopian tubes are also removed. If both ovaries are removed, you will go into menopause (change of life) if you have not done so already.

To decide what stage the cancer is in, lymph nodes in the pelvis and around the aorta will also need to be removed (see below). This can be done at the same time as the hysterectomy or as a separate procedure.

Lymph node surgery

Lymph node removal: When lymph nodes are taken out it is called "lymph node dissection." In this operation, lymph nodes from the pelvis and the area around the main artery that carries blood from the heart (the aorta) are removed. They are looked at to see if they contain cancer cells. This can be done at the same time as the hysterectomy or with a laparoscope (explained below).

Laparoscopic lymph node sampling: When only a few of the lymph nodes are removed, it is called "lymph node sampling." Thin tubes are put into the belly (abdomen) through very small incisions. Small tools can be controlled through the tubes and the doctor can take out some lymph nodes. Studies are going on to find out whether this method is as good as removing all the lymph nodes to treat endometrial cancer.

Pelvic washings

To do a pelvic washing, the surgeon "washes" the abdominal and pelvic areas with salt water (saline) and then sends the fluid to the lab to see if it contains cancer cells.

Other tests that may be used for staging

Omentectomy: The omentum is a layer of fatty tissue that covers the abdominal contents like an apron. Cancer sometimes spreads to this tissue. When this tissue is removed, it is called an omentectomy. Sometimes the omentum is removed during a hysterectomy to see if cancer has spread there.

Peritoneal biopsies: The tissue lining the pelvis and abdomen is called the peritoneum. Peritoneal biopsies remove small pieces of this lining to check for cancer cells.

Tumor debulking

If cancer has spread throughout the abdomen, the surgeon may try to remove as much of the tumor as possible. This is called debulking. Debulking a cancer can help other treatments work better. Tumor debulking is helpful for other types of cancer, but it isn't clear yet if it will help women with endometrial cancer live longer.

Recovery after surgery

For an abdominal hysterectomy, the hospital stay is usually 3 to 7 days. Complete recovery takes about 4 to 6 weeks.

Side effects

A woman cannot become pregnant after a hysterectomy. If change of life had not happened before surgery, removing the ovaries will cause it to happen. Problems from surgery are rare but could include too much bleeding, wound infection, and damage to the urinary or intestinal systems.

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 it can come from radioactive materials placed near the tumor. This is called brachytherapy. In some cases, both types of radiation treatment are used.

How much of the pelvis needs to have radiation treatment depends on how far the cancer has spread.

Brachytherapy

In cases where only the upper third of the vagina needs to be treated after surgery, radioactive pellets or seeds can be put into place for a short time. They are put in through the vagina. With brachytherapy there is little effect on nearby structures, such as the bladder or rectum.

This treatment is given in the radiation suite of the hospital or care center. About 4 to 6 weeks after surgery, the doctor puts the pellets of radioactive material into the vagina. More than one treatment may be needed. The number of treatments depends on the strength of the dose. For endometrial cancer, high dose radiation is often given weekly or even daily for at least 3 doses.

External radiation

This method of giving radiation is like a regular x-ray but it takes longer. It is most often given 5 times a week, for 4 to 6 weeks. While treatment itself takes less than a half-hour, the daily trips may hard to manage.

Side effects of radiation therapy

  • tiredness (fatigue)
  • upset stomach
  • loose bowels (diarrhea)
  • nausea and vomiting
  • skin changes like redness and soreness
  • problems passing urine
  • the vagina may become dry, or shorter, or more narrow (this is called vaginal stenosis), causing pain during sex
  • early menopause
  • weakened bones in the pelvis

Radiation can also lead to low blood counts, causing low red blood cells and low white blood cells. The blood counts usually return to normal after radiation is stopped.

If you are having side effects from radiation, talk to your doctor. There are things you can do to get relief from these problems or to prevent them from happening.

Chemotherapy

Chemotherapy (often called "chemo") is the use of cancer-fighting drugs to kill cancer cells. Usually these 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. One or more drugs may be used.

While these drugs kill cancer cells, they can also damage some normal cells. This can cause side effects. Which side effects happen will depend on the type of drugs given, the amount or dose, how often treatment is done, and how long treatment lasts. Common side effects are:

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

Most side effects go away after treatment ends. If you have problems with side effects, talk with your doctor or nurse, as there are often ways to help.

Hormone therapy

Hormone therapy is the use of hormones or hormone-blocking drugs to fight cancer. Below are some of the types of hormone therapy that might be used.

Progestins: Progesterone-like drugs can be used to slow the growth of cancer cells. The drugs are usually taken as pills or injections.

Tamoxifen: Tamoxifen is a drug often used to treat breast cancer. It may also be used to treat advanced endometrial cancer or endometrial cancer that has returned (recurrent endometrial cancer).

GNRH (Gonadotropin-releasing hormone): These drugs switch off the estrogen made by the ovaries in women who have not gone through change of life. The drugs are injected every 1 to 3 months.

Aromatase inhibitors: After the ovaries are removed (or if they are not working), estrogen is still made in fat tissue. This becomes the body's main source of estrogen. Drugs called aromatase inhibitors can stop this estrogen from being formed and lower estrogen levels even further. These drugs are still being studied, and their role in endometrial cancer treatment is not clear.

Endometrial cancer survival by stage

The 5-year relative survival rate is the percentage of patients who have not died from endometrial cancer at least 5 years after the cancer is found. Those who die of other causes are not counted. Of course, patients might live more than 5 years after diagnosis.

When all cases of endometrial cancer are looked at together, the 5-year relative survival rate is about 88%. Most of these cancers are found at an early stage, which has a 5-year survival rate of over 95%. But the outlook (prognosis) for any one woman depends on the stage of her cancer as well as several other factors.

These numbers give you an overall picture, but keep in mind that every woman's situation is unique and the statistics can't predict exactly what will happen in your case. Talk with your cancer care team if you have questions about your personal chances of a cure, or how long you might survive your cancer. They know your situation best.

Colon and Rectum Cancer

What Is Colorectal Cancer?
Colorectal cancer is a term used to refer to cancer that starts in either the colon or the rectum. Colon cancer and rectal cancer have many features in common. They are discussed together here except for the section about treatment, where they are discussed separately.

The normal digestive system

Colon and rectal cancers begin in the digestive system, also called the GI (gastrointestinal) system (see the picture below). This is where food is processed to create energy and rid the body of solid waste matter (stool). In order to understand colorectal cancer, it helps to know some basics about the normal structure and function of the digestive system.

After food is chewed and swallowed, it travels down to the stomach. There it is partly broken down and sent to the small intestine. The word "small" refers to the width of the small intestine. In fact, the small intestine is the longest part of the digestive system -- about 20 feet.

The small intestine also breaks down the food and absorbs most of the nutrients. The small intestine leads to the large intestine (also called the large bowel or colon), a muscular tube about 5 feet long. The colon absorbs water and nutrients from the food and also serves as a storage place for waste matter. The waste matter moves from the colon into the rectum, the last 6 inches of the digestive system. From there the waste passes out of the body through the opening called the anus.






The wall of the colon and rectum has several layers of tissues. Colorectal cancer starts in the inner layer and can grow through some or all of the other layers. Knowing a little about these layers is helpful because the stage (extent of spread) of a cancer depends to a great degree on how deep the cancer goes into these layers.

Abnormal growths in the colon or rectum

Cancer that starts in these different areas may cause different symptoms. But colon cancer and rectal cancer have many things in common. In most cases, colorectal cancers develop slowly over many years. We now know that most of these cancers begin as a polyp--a growth of tissue that starts in the lining and grows into the center of the colon or rectum. This tissue may or may not be cancer. A type of polyp known as an adenoma can become cancerous. Removing a polyp early may prevent it from becoming cancer.

Over 95% of colon and rectal cancers are adenocarcinomas. These are cancers that start in the cells that line the inside of the colon and rectum. There are some other, more rare, types of tumors of the colon and rectum, but the facts given here refer only to adenocarcinomas.

What Causes Colorectal Cancer?
While we do not know the exact cause of most colorectal cancers, there are certain known risk factors. A risk factor is something that affects a person's chance of getting a disease. Some risk factors, like smoking, can be controlled. Others, such as a person's age, can't be changed.

But risk factors don't tell us everything. Having a risk factor, or even several risk factors, does not mean that you will get the disease. And some people who get the disease may not have any known risk factors. Even if a person with colorectal cancer has a risk factor, it is often very hard to know what part that risk factor may have contributed to the cancer.

Researchers have found several risk factors that may increase a person's chance of getting polyps or colorectal cancer.

Risk factors you cannot change

Age: The chances of having colorectal cancer go up after age 50. More than 9 out of 10 people found to have colorectal cancer are older than 50.

Having had polyps or colorectal cancer before: Some types of polyps increase the risk of colorectal cancer, especially if they are large or if there are many of them. If you have had colorectal cancer (even if it has been completely removed), you are more likely to have new cancers start in other areas of your colon and rectum. The chances of this happening are greater if you had your first colorectal cancer when you were younger than age 60.

Having a history of bowel disease: Two bowel diseases, called ulcerative colitis and Crohn�s disease, increase the risk of colon cancer. In these diseases, the colon is inflamed over a long period of time. If you have either of these diseases your doctor may want you to have colon screening testing more often. (These diseases are different than irritable bowel syndrome (IBS), which does not carry an increased risk for colorectal cancer.)

Family history of colorectal cancer: If you have close relatives who have had this cancer, your risk might be increased. This is especially true if the family member got the cancer before age 60. People with a family history of colorectal cancer should talk to their doctors about when and how often to have screening tests.

Certain family syndromes: A syndrome is a group of symptoms. For example, in some families members tend to get a type of syndrome called FAP that involves having hundreds of polyps in their colon or rectum. Cancer often develops in 1 or more of these polyps.

If your doctor tells you that you have a condition that makes you or your family members more likely to get colorectal cancer, you will probably need to begin colon cancer testing at a younger age and you might want to talk about genetic counseling.

Race or ethnic background: Some racial and ethnic groups such as African Americans and Jews of Eastern European descent (Ashkenazi Jews) have a higher colorectal cancer risk. All of the reasons for this are not yet understood.

Risk factors linked to things you do

Several lifestyle-related factors have been linked to colorectal cancer. In fact, the links between diet, weight, and exercise and colorectal cancer risk are some of the strongest for any type of cancer.

Certain types of diets: A diet that is high in red meats (beef, lamb, or liver) and processed meats such as hot dogs, bologna, and lunch meat can increase your colorectal cancer risk. Cooking meats at very high heat (frying, broiling, or grilling) can create chemicals that might increase cancer risk. Diets high in vegetables and fruits have been linked with a lower risk of colorectal cancer.

Lack of exercise: Getting more exercise may help reduce your risk.

Overweight: Being very overweight increases a person's risk of dying from colorectal cancer.

Smoking: Most people know that smoking causes lung cancer, but long-time smokers are more likely than non-smokers to die of colorectal cancer. Smoking increases the risk of many other cancers, too.

Alcohol: Heavy use of alcohol has been linked to colorectal cancer.

Diabetes: People with type 2 diabetes have an increased chance of getting colorectal cancer. They also tend to have a higher death rate from this cancer.

Risk factors that are less certain

Night-shift work: One study suggests that working a night shift at least 3 nights a month for at least 15 years might increase the risk of colorectal cancer in women. More research is needed to check out this finding.

Other cancers and their treatment: A recent report on testicular cancer survivors found that these men had a higher rate of colorectal cancer. Men who receive radiation therapy for prostate cancer have been reported to have a higher risk of rectal cancer, too.

The American Cancer Society and several other medical organizations recommend earlier testing for people with increased colorectal cancer risk. These recommendations differ from those for people at average risk. For more information, talk with your doctor.

How Is Colorectal Cancer Found?
Colorectal cancer screening tests

Screening tests are used to look for disease in people who do not have any symptoms. In many cases, these tests can find colorectal cancers at an early stage and greatly improve the chances of successful treatment. Screening tests can also help prevent some cancers by allowing doctors to find and remove polyps that might become cancer. The tests used to screen for polyps and colorectal cancer can be divided into 2 broad groups:

  • Tests that can find both colorectal polyps and cancer: These tests are done either with a scope inserted into the rectum or with special x-ray tests. Polyps found before they turn into cancer can be removed, so these tests may prevent colorectal cancer. Because of this, they are preferred if they are available and you are willing to have them.
  • Tests that mainly find cancer: These involve testing the stool (feces) for signs of cancer. These tests are easier to have done, but they are less likely to find polyps.

Tests that can find both colorectal polyps and cancer

Flexible sigmoidoscopy (flex-sig): A sigmoidoscope is a thin, flexible, lighted tube about the thickness of a finger. It is placed into the lower part of the colon through the rectum. This allows the doctor to look at the inside of the rectum and part of the colon for cancer or polyps. Because the tube is only about 2 feet long, the doctor is only able to see about half of the colon. The test can be uncomfortable, but it should not be painful. Before the test, you will need to take some medicine to clean out your colon. If a small polyp is found your doctor may remove it during this test. If an adenoma polyp or colorectal cancer is found during the flex-sig, you will need to have a colonoscopy to look for polyps or cancer in the rest of the colon.

Colonoscopy: A colonoscope is a longer version of the sigmoidoscope. It is used the same way but allows the doctor to see the entire colon. If a polyp is found, the doctor may remove it. If anything else looks abnormal, a biopsy might be done. To do this, a small piece of tissue is taken out through the colonoscope. The tissue is sent to the lab to see if cancer cells are present.

Before the test: The colon and rectum must be empty and clean. You will need to some medicine to clean out your colon the day before the test and maybe an enema that morning. Your doctor will give you exact instructions. Be sure to read these carefully a few days ahead of time, since you may need to shop for special supplies and get laxatives from a drug store. If you are not sure about anything, call the doctor's office and go over them step by step with the nurse. Many people find the bowel preparation to be the most unpleasant part of the test, as you will most likely be in the bathroom quite a bit. You may be given other instructions, too, such as foods to avoid for a certain amount of time before the test.

During the test: The test itself usually takes about 30 minutes, but it may take longer if a polyp is found and removed. Before the test begins, you will be given medicine through your vein to make you feel comfortable and sleepy. You may be awake, but you may not be aware of what is going on and may not remember the test afterward. Most people will be fully awake by the time they get home from the test.

You may need to have someone drive you home from the test because the medicine used can affect your ability to drive. Some doctors require that someone drive you home.

Double contrast barium enema (DCBE): To do this test a chalky substance is used to partly fill and open up the colon. Air is then pumped in to cause the colon to expand. This allows good x-ray pictures to be taken. If an area does not look normal you will need to have a colonoscopy.

The preparation for this test is similar to that for the colonoscopy (above), although for the DCBE you will not be given drugs to make you sleepy.

Virtual colonoscopy: You might think of this as a super x-ray or CT scan of the colon. The CT scanner takes many pictures as it rotates around you while you lie on a table. A computer then combines these pictures into images of slices of the part of your body being studied. Virtual colonoscopy ( also calledCT colonography) involves the use of special computer programs to create both 2 dimensional x-ray pictures and a 3-D "fly-through" view of the inside of the colon and rectum, which allows the doctor to look for polyps or cancer.

This test may be useful for some people who can't have or don't want to have tests such as colonoscopy. It can be done fairly quickly and you do not need sedation. But while this test is not invasive like colonoscopy, it still requires the same type of bowel preparation. If polyps or other problems are seen on this test, a colonoscopy will likely be needed to remove them or to explore them fully.

Tests that mainly find colorectal cancer

These tests are used to find small amounts of hidden (occult) blood in the stool. Most people find these tests to be easier because they can often be done at home. But they are not as good at finding polyps as the tests described above, and a positive result on one of these screening tests will likely mean you will need a test such as colonoscopy.

These tests have different names such as FOBT, FIT, and iFIT. They are all alike in that you will need to collect samples of your stool (bowel movement) to be sent to a lab for testing. They differ in the exact way in which you collect the samples and in how the samples are studied in the lab.

If you are having one of these tests, the doctor or nurse will give you a kit with exact instructions on what to do ahead of time (there may be some limits on what you can eat or drink or medicines that you take) and how to collect the samples.

Some people who are given the kits never do the test or don't give it to their doctor because they worry that they might not have followed the instructions right. Be sure to talk to your doctor or nurse if you have any questions about what you should do or how to collect the samples. The most important thing is to get the test done.

Most of these tests need to be done every year, and, as mentioned before, if the lab spots any problems, you will need to have more tests, such as a colonoscopy.

Preventing colorectal cancer or finding it early

Colon cancer begins with a growth (a polyp) that is not yet cancer. Testing can help your doctor tell whether there is a problem, and some tests can find polyps before they become cancer. Most people who have polyps removed never get colon cancer. If colon cancer is found, you have a good chance of beating it with treatment if it is found early. Testing can find it early.

The American Cancer Society believes that preventing colorectal cancer (and not just finding it early) should be a major reason for getting tested. Finding and removing polyps keeps some people from getting colorectal cancer. Tests that have the best chance of finding both polyps and cancer should be your first choice if these tests are available to you and you are willing to have them.

Doctors will take into account a number of factors when they recommend the tests you should have, how often you should have them, and when you should begin testing. These factors include the following:

  • Whether you are at average, increased, or high risk for colorectal cancer
  • If you are at increased or high risk, the type of test used and how often it is done will further depend on whether you have had polyps, cancer, or certain other diseases, as well as aspects of your family history.

In general, both men and women at average risk of colorectal cancer should begin screening tests at age 50. But you should talk with your doctor about your own health and your family history so that you can choose the best screening plan for you.

Insurance coverage for colorectal cancer screening

Although there are good colorectal cancer screening tests, not enough people have them done. Some of the reasons could include the lack of awareness of screening tests, costs, and lack of health insurance coverage and/or benefits.

Laws regarding insurance coverage for colorectal cancer screening tests vary by state. The same is true of state Medicaid programs. For people with Medicare, coverage begins at age 50 for the most common colorectal cancer screening tests.

For more information on insurance coverage for colorectal cancer screening tests, please see the separate American Cancer Society document, Colorectal Cancer: Early Detection.

How is colorectal cancer diagnosed?

Most people with early colon cancer don�t have symptoms. Symptoms usually appear with more advanced disease. If something suspicious turns up as a result of screening or if you have symptoms, you will need further tests.

Signs and symptoms of colorectal cancer

  • a change in bowel habits such as diarrhea, constipation, or narrowing of the stool that lasts for more than a few days
  • a feeling that you need to have a bowel movement that doesn't go away after doing so
  • rectal bleeding, dark stools, or blood in the stool (often, though, the stool will look normal)
  • cramping or stomach pain
  • weakness and tiredness.

Most of these symptoms are more likely to be caused by something other than colorectal cancer. Still, if you have any of these problems, it's important to see your doctor right away so the cause can be found and treated, if needed.

If there is any reason to suspect colon or rectal cancer you will need to have more tests to find out if the disease is really present and, if so, to see how far it has spread. Some of these tests are the same ones that are used for screening people who do not have symptoms. (See the section below, "Tests to look for colorectal polyps and cancer.")

Medical history and physical exam: Your doctor will ask you questions about your health, your family history, and she will also do a complete physical exam.

Blood tests

Your doctor may order certain blood tests to help find out if you have colorectal cancer. People with colorectal cancer often become anemic because of bleeding from the tumor. You might also have blood tests to check your liver function because colorectal cancer can spread to the liver. There are other substances (tumor markers) in the blood that can help tell how well treatment is working. But these tumor markers are not used to find cancer in people who have not had cancer and who appear to be healthy. They are most often used for follow-up of people who have already been treated for colorectal cancer.

Tests to look for colorectal polyps or cancer

If symptoms or the results of the physical exam or blood tests suggest that you might have colorectal cancer, your doctor may want to do some more tests.

Biopsy: In a biopsy, the doctor removes a small piece of the tissue that does not look normal. This is done during a colonoscopy. The tissue is sent to the lab where it is looked at under a microscope to see if cancer is present. While other tests may suggest colorectal cancer, a biopsy is the only way to know this for sure.

Imaging tests

These tests, described below, make pictures of the inside of your body. Imaging tests may be done for a number of reasons, such as to help find out whether a suspicious area might be cancer, to learn how far cancer may have spread, and to help learn if treatment is working.

Computed tomography (CT or CAT) scan

A CT scan uses x-rays to take many pictures of the body that are then combined by a computer to give a detailed picture. A CT scan can often show whether the cancer has spread to the liver, lungs, or other organs. CT scans take longer than regular x-rays. The patient has to lie still on a table while the CT scan is being done. A contrast "dye" may be injected or a special drink used to help outline the area being viewed.

CT scans can also be used to guide a biopsy needle into a tumor or metastasis. For this to be done, the patient remains on the CT table, while a radiologist moves a biopsy needle through the skin and toward the mass. A tiny fragment of tissue or a thin cylinder of tissue about ½ inch long and less than 1/8 inch wide is then removed and looked at under a microscope.

A new way to use a CT scan is to do a "virtual colonoscopy." After stool is cleaned from the colon and the colon is filled with air, a computer can then put together a picture of the inside of the colon. This method requires the same preparation as for a colonoscopy and there is some discomfort from the bowel being filled with air. If anything not normal is seen, a follow-up colonoscopy will be needed.

Ultrasound

Ultrasound uses sound waves to produce a picture of the inside of the body. Most people know about ultrasound because it is often used to look at a baby during pregnancy. This is an easy test to have. You simply lie on a table while a kind of wand is moved over your skin.

Two special types of ultrasound might be used for people with colon or rectal cancer. In one, the wand that gives off sound waves is placed into the rectum to look for cancer there and to see if it has spread to nearby organs or tissues. In the other test, used during surgery, the wand is placed against the surface of the liver to see if the cancer has spread there.

Magnetic resonance imaging (MRI) scan

Like CT scans, MRIs show a cross-section of the body. But, MRI uses radio waves and strong magnets instead of radiation to take pictures. As with CT scans, a contrast dye may be injected, although this is used less often. MRI scans are helpful in looking at the brain and spinal cord. They take longer than CT scans and you may have to be placed inside a narrow tube for the test. This can feel confining and upset people with a fear of closed spaces. The machine also makes a thumping noise, but some places will provide headphones with music to block this out.

Chest X-ray

This test may be done to see whether colorectal cancer has spread to the lungs.

Positron emission tomography (PET) scan

In this test, a type of radioactive sugar is injected into a vein. Then you are put into the PET machine where a special camera can detect the radioactivity. The cancer cells absorb high amounts of the sugar and show up on the pictures as dark "hot spots." PET is useful when your doctor thinks the cancer has spread, but doesn't know where. PET scans are now more accurate because they can be combined with a CT scan.

Angiography

For this test, a tube (called a catheter) is placed into a blood vessel and moved until it reaches the area to be studied. Then a dye is injected and a series of x-ray pictures is taken. When the pictures are done, the catheter is taken out. Surgeons sometimes use this to find blood vessels next to cancer that has spread to the liver. The cancer can then be removed without causing a lot of bleeding.

How Is Colorectal 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.

The 4 main types of treatment for colorectal cancer are

  • surgery
  • radiation therapy
  • chemotherapy (often called just "chemo")
  • targeted therapies (called monoclonal antibodies)

Depending on the stage of your cancer, 2 or more types of treatment may be used at the same time, or used one after the other.

Take your time and think about all of your treatment choices. You may want to get a second opinion. This can give you more information and help you feel better about the treatment plan you choose. Your chances of having a good outcome are highest in the hands of a medical team that has experience in treating colorectal cancer.

Surgery

The types of surgery used to treat colon and rectal cancers are slightly different and are described separately.

Colon surgery

Surgery is often the main treatment for earlier stage colon cancer. The surgery is called a colectomy or a segmental resection. Usually the cancer and a length of normal colon on either side of the cancer (as well as nearby lymph nodes) are removed. The 2 ends of the colon are then sewn back together. For colon cancer, a colostomy (an opening in the abdomen for getting rid of body wastes) is not usually needed, although sometimes a short-term colostomy may be done to allow the colon to heal.

Most often, surgery is done through an incision in the abdomen, but for some earlier stage cancers a different approach might be an option. In laparoscopic-assisted colectomy, instead of 1 long incision in the abdomen, the surgeon makes several small ones. Special long instruments are put into these small openings and used to remove part of the colon and lymph nodes. This method appears to be about as likely to cure the cancer as the standard approach for earlier stage cancers and patients usually recover faster than they do after the usual operations. But the surgery calls for special skill. If you are thinking about this approach, be sure to look for a skilled surgeon who has done a lot of these operations.

Some very early colon cancers (stage 0 and some early stage I tumors) or polyps can be removed using a colonoscope. When this is done, the surgeon does not have to cut into the abdomen. Early stage cancers that are only on the surface of the colon lining can be removed along with a small amount of nearby tissue. For a polypectomy, the cancer is cut out across the base of the polyp's stalk, the area that looks like the stem of a mushroom.

Rectal surgery

Surgery is usually the main treatment for rectal cancer, too, although radiation and chemotherapy will often be given before surgery. There are several types of surgery for rectal cancer.

Some operations (such as polypectomy, local excision, and local transanal resection) can be done with instruments placed into the anus, without having to cut through the skin. One of these methods might be used to remove some stage I cancers that are fairly small and not too far from the anus.

For some stage I, and most stage II or III rectal cancers, other types of surgery may be done. These are described here:

Low anterior resection: This approach is used for cancers near the upper part of the rectum, close to where it connects with the colon. The surgeon makes the incision only in the abdomen. Then he removes the cancer and a small amount of normal tissue on either side of the cancer, along with nearby lymph nodes and a large amount of fatty and fibrous tissue around the rectum. The anus is not affected. After the surgery, the colon is reattached to the anus and waste leaves the body in the usual way.

Abdominoperineal (AP) resection: For cancers in the lower part of the rectum, close to its outer connection to the anus, an abdominoperineal (AP) resection is done. For this the surgeon makes 1 incision in the abdomen, and another in the area around the anus. Because the anus is removed, a colostomy is needed. A colostomy is an opening of the colon in the front of the abdomen. It is used for the body to get rid of solid body waste (feces or stool).

Pelvic exenteration: If the rectal cancer is growing into nearby organs, more extensive surgery is needed. In a pelvic exenteration the surgeon removes the rectum as well as nearby organs such as the bladder, prostate, or uterus if the cancer has spread to these organs. A colostomy is needed after this operation. If the bladder is removed, a urostomy (an opening to collect urine) is also needed.

Side effects of colorectal surgery

Side effects of surgery depend on several things, such as the extent of the operation and a person's general health before surgery. Most people will have at least some pain after the operation, but this can usually be controlled with medicines if needed. Eating problems usually inprove within a few days of surgery.

Possible side effects of surgery include bleeding from the surgery, blood clots in the legs, and damage to nearby organs during the operation. Rarely, the connections between the ends of the intestine may not hold together completely and leak. If an infection occurs, it is possible that the incision might open up, causing an open wound. Later, after the surgery, you might develop scar tissue in your abdomen (called adhesions) that could cause the bowel to become blocked.

If you have a colostomy or a urostomy, you will need help in learning how to manage it. This can be done by specially trained nurses. They will usually see you before your operation and again afterwards for more training.

Colorectal surgery and sex

If you are a man, an AP resection can cause you to have "dry" orgasms. That is, the feeling of pleasure will most likely still be there, but no semen comes out. In some cases an AP resection may make you unable to have erections or reach orgasm. In other cases your pleasure at orgasm may become less intense. Normal aging may cause some of these changes, but surgery can increase them.

For some men, the surgery causes the semen to go backward into the bladder. This is not harmful. But if you still want to father a child, you should talk to your doctor about how the surgery will affect you and what might be done to achieve a pregnancy.

If you are a woman having colorectal surgery, you should not normally find any loss of sexual function. Scar tissue may sometimes cause pain or discomfort during intercourse. And if the uterus is removed, pregnancy will not be possible.

For men and women, a colostomy can affect your body image and your sexual comfort level. While you may need to make some adjustments, it should not keep you from having an enjoyable sex life.

The American Cancer Society has more information for both men and women about sexuality and cancer. Please see the list of booklets at the end of this article.

Surgery for colorectal cancer that has spread

Sometimes, surgery for cancer that has spread to other organs can help you to live longer or, depending on the extent of the disease, may even cure you. If the colorectal cancer has spread to a few areas in liver or lungs (and nowhere else), the cancer can sometimes be removed by surgery.

For spread to the liver, there are other methods besides surgery which might be used to destroy the cancer. These include methods to block the blood supply to the tumor or to destroy the cancer through freezing or by heating with microwaves. These methods are not meant to cure the cancer.

Radiation therapy for colon and rectal cancer

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 (brachytherapy or internal or implant radiation).

After surgery, radiation can kill small areas of cancer that may not be removed during surgery. If the size or location of a tumor makes surgery hard, radiation may be used before the surgery to shrink the tumor. Radiation can also be used to ease symptoms of advanced cancer such as intestinal blockage, bleeding, or pain.

The main use for radiation therapy in people with colon cancer is when the cancer has attached to an internal organ or the lining of the abdomen. If this happens, the doctor can't be sure that all the cancer has been removed, and radiation therapy is used to kill the cancer cells left behind after surgery. For rectal cancer, radiation is also given to prevent the cancer from coming back in the place where it started and to treat local recurrences that are causing symptoms such as pain. Radiation is seldom used to treat metastatic colon cancer.

External-beam radiation therapy: In this method, radiation is focused on the cancer from a machine outside the body. This approach is most often used for people with colon or rectal cancer. Treatments are given 5 days a week for several weeks. Each treatment lasts only a few minutes although the setup time -- getting you into place for treatment -- usually takes longer.

A different approach may be used for some cases of rectal cancer with small tumors. The radiation can be aimed through the anus and reaches the rectum without passing through the skin of the abdomen. This means it is less likely to damage nearby tissues and cause side effects.

Brachytherapy (internal radiation therapy): In this method, small pellets or seeds of radioactive material are placed next to or directly into the cancer. The radiation travels only a short distance, limiting the effects on nearby healthy tissues. This method is sometimes used in treating people with rectal cancer, particularly sick or older people who would not be able to withstand surgery.

Side effects of radiation therapy

Side effects of radiation therapy for colon or rectal cancer include mild skin irritation, nausea, diarrhea, trouble controlling your bowel, rectal or bladder irritation, or tiredness. Sexual problems may also occur. Side effects often go away after treatment is over. If you have these or other side effects, talk to your doctor. There are often ways to reduce or relieve many of these problems.

Chemotherapy

Chemotherapy (often called simply "chemo") is the use of drugs to fight cancer. The drugs may be injected into a vein or given by mouth. These drugs enter the bloodstream and spread throughout the body, making the treatment useful for cancers that have spread to distant organs.

Chemo after surgery can increase the survival rate for patients with some stages of colorectal cancer. Chemo can also help relieve symptoms of advanced cancer.

In some cases, chemo drugs can be injected into an artery leading to the part of the body with the tumor. This approach is called regional chemotherapy. Since the drugs go straight to the cancer cells, there may be fewer side effects.

Side effects of chemotherapy

While chemo kills cancer cells, it also damages some normal cells and this can cause side effects. These side effects will depend on the type of drugs given, the amount given, and how long treatment lasts. Side effects could include the following:

  • diarrhea
  • nausea and vomiting
  • loss of appetite
  • hair loss
  • hand and foot rashes and swelling
  • mouth sores
  • increased chance of infection
  • easy bleeding or bruising after minor cuts or injuries
  • severe tiredness (fatigue)

Most of the side effects go away when treatment is over. For example, hair will grow back after treatment ends, though it may look different. Anyone who has problems with side effects should talk with their doctor or nurse, as there are often ways to help.

Targeted therapies

Targeted therapies are drugs that attack a part of cancer cells that makes them different from normal cells. Because these drugs affect only cancer cells, they often cause fewer side effects than chemo. Man-made proteins called monoclonal antibodies have been approved for use, along with chemo, against colorectal cancer.

Colorectal cancer survival rates

The 5-year survival rate is the percentage of patients who are alive 5 years after their cancer is found (leaving out those who die of other causes). Many of these patients live much longer than 5 years. While the numbers below are among the most current we have, they are from people who were first treated many years ago. Because cancer treatment continues to improve, the survival rates for people now may be higher.

Survival rates for colon cancer by stage

Stage I 93%
Stage IIA 72%
Stage IIB 72%
Stage IIIA 83%*
Stage IIIB 64%
Stage IIIC 44%
Stage IV 8%

*In this study, survival was better for stage IIIA than for stage IIB. The reasons for this are not clear, and it is not known if this is still the case.

Relative survival rates for rectal cancer by stage

Stage Relative 5-year Survival Rate
Stage I 92%
Stage II 73%
Stage III 56%
Stage IV 8%


These numbers provide an overall picture, but keep in mind that every person is unique and statistics can’t predict exactly 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.

Childhood Non-Hodgkin's Lymphoma

What Is Childhood Non-Hodgkin Lymphoma?

Lymphoma is the third most common childhood cancer. There are 2 main types of lymphomas. The first is called Hodgkin (Hodgkins) lymphoma or Hodgkin disease. It is named after Dr. Hodgkin, who first described it in 1832. All other types of lymphoma are called non-Hodgkin lymphoma (non-Hodgkins lymphoma), or NHL. These 2 types of lymphoma are very different. They behave differently and they need different treatments. The information here covers only NHL in children.

Lymphoma is a type of cancer that starts in lymphoid tissue. Other types of cancer can start in other organs and then spread to lymphoid tissue, but these cancers are not lymphomas.

What Is Lymphoid Tissue?

Lymphoid (sometimes called lymphatic) tissue includes the lymph nodes and other organs that are part of the body's system that forms blood and protects against germs. The immune system is made up mostly of lymphoid tissue. This tissue consists of several types of cells that work together to resist infections. Lymphoid tissue is found in many places throughout the body.

The main cell type within lymphoid tissue is the lymphocyte. There are two major types of lymphocytes: B cells and T cells. These are the cells from which lymphomas develop. In fact, there are several sub-types of T cells and several stages of T-cell and B-cell development. Normal T cells and B cells do different jobs within the immune system. These differences play a part in helping doctors identify the different types of lymphomas.

Types of Lymphoid Tissue

Lymph nodes are small, bean-shaped organs found in many places throughout the body. The lymph nodes make and store white blood cells that fight infection. Lymph nodes get bigger when they fight infection, especially in infants and children.

Lymph vessels, narrow tubes something like blood vessels, connect the lymph nodes. These vessels carry a clear fluid that contains white blood cells. Other parts of the lymphatic system are described below. Lymphoid tissue is also found scattered within other organs such as the stomach and intestines.

The spleen is an organ found under the lower part of the rib cage, on the left side of the body. The spleen is the largest collection of lymph tissue in the body.

The thymus gland is an organ found in front of the heart. The thymus plays a vital role in the development of T cells, a kind of white blood cell. It becomes less active as a person gets older but it continues to function as part of the immune system.

Adenoids and tonsils are collections of lymph tissue found at the back of the throat. They are easy to see if they become enlarged during an infection or if they become cancerous.

The bone marrow (the soft, inner part of bones) makes red blood cells, clotting cells (platelets), and white blood cells. In infants, bone marrow is found in almost all bones of the body, but by the teenage years it is found mostly in the flat bones (skull, shoulder blade, ribs, hip bones) and in the back bones.

Types of Non-Hodgkin Lymphomas

Lymphomas are often divided into groups by how the cancer cells look under a microscope and their pattern of growth within the lymph node. The classification system is fairly complex. Size is described as large or small. Shape is described as cleaved (having folds) or non-cleaved. The growth pattern may be either diffuse (scattered) or follicular (in clusters of cells). Lymphomas of children are also high-grade, meaning they grow very quickly.

Nearly all non-Hodgkin lymphomas in children belong to 1 of these 3 types:

  • lymphoblastic lymphoma
  • small non-cleaved cell (Burkitt) lymphoma
  • large cell lymphoma

The 3 types are treated very differently.

Lymphoblastic lymphomas account for just under one third of lymphomas in children. They are most common in teenagers, and boys are affected twice as often as girls. This type of lymphoma tends to spread very quickly to the bone marrow, other lymph nodes, the surface of the brain, and membranes around the heart. Because this type of lymphoma can grow so fast, it needs to be found and treated promptly.

The cancer cells of this lymphoma are the same as those in a type of leukemia. If more than one fourth of the bone marrow is involved, the disease is then called leukemia and treated as such.

Small non-cleaved cell lymphoma accounts for about half of the cases of childhood NHL in this country. It is most often seen in boys around the ages of 5 to 10. This type of lymphoma is further divided into 2 groups: Burkitt type (also called Burkitt's lymphoma) and non-Burkitt type. Children with both types have the same treatment.

In certain areas of Africa, Burkitt type is found much more often than it is here. This lymphoma is one of the fastest growing cancers known. It may spread to many organs including the surface of the brain or the inside of the brain. Because of this, it must be found and treated quickly.

Large cell lymphoma (LCL) accounts for about one fourth of all non-Hodgkin lymphoma in children. It may develop in lymphoid tissue in the neck, the area near the thymus, throat, or abdomen. Early on it may spread to the skin or tissues under the skin. Unlike the other 2 types, it seldom spreads to the bone marrow or brain. Nor does it grow as quickly as the other types.

What Causes Childhood Non-Hodgkin Lymphoma?

While we do not yet know exactly what causes non-Hodgkin lymphoma, we do know that certain risk factors are linked to the disease. A risk factor is anything that increases 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 several, doesn�t mean that a person will get the disease.

As a rule, lifestyle-related risk factors such as diet or smoking are the least important part of childhood cancer risk. Many of the risk factors for non-Hodgkin lymphoma appear to be linked to problems with the immune system. These problems may be present at birth or they may be caused by infections or drugs used to treat other diseases.

Certain genetic diseases cause some children to be born with an immune system that doesn�t work well. Because of this, these children can develop serious infections. They have an increased risk of non-Hodgkin lymphoma as well.

Children treated with radiation for some other cancers have a slightly higher risk of getting this lymphoma later in life. Patients treated with both chemotherapy and radiation are more likely to develop leukemias or non-Hodgkin lymphoma years later as a result of this treatment.

People with transplanted organs (kidney, heart, liver) are treated with drugs that weaken their immune system. This is done to keep the immune system from attacking the new organs. But at the same time, this process can increase the risk of non-Hodgkin lymphoma. The exact risk depends on which drugs were used.

Infection with the virus that causes AIDS (HIV) also weakens the immune system and is a risk factor for this cancer.

In areas of Africa where Burkitt�s lymphoma is common, chronic infection with both malaria and the Epstein-Barr virus (EBV) is an important risk factor.

It is important to remember that most children with non-Hodgkin lymphoma have no known risk factors. There is nothing these children or their parents could have done to prevent this cancer.

How Is Childhood Non-Hodgkin Lymphoma Found?


The best course of action is to pay prompt attention to any signs or symptoms of the disease. These symptoms will vary depending on the location of the tumors.

If the lymphoma is in the lymph nodes close to the surface of the body (on the sides of the neck, in the underarm area, above the collar bone, or the groin, etc.), there will be swelling in that area. Usually the child, a parent, or the doctor will notice this.

If the cancer is in the abdomen, then that area can become very swollen. When the cancer causes the lymph tissue near the kidney to swell, passage of urine through that area can become blocked, causing low urine output, tiredness, loss of appetite, nausea, or swelling in the hands or feet. The cancer may also block feces moving through the bowel. This can cause nausea, vomiting, and severe pain in the stomach area.

If the lymphoma is in the thymus or the lymph nodes inside the upper part of the chest, it can create pressure on the windpipe. This can lead to coughing, shortness of breath, or even suffocation. The large vein (called the SVC) that carries blood from the head and arm back to the heart passes next to the thymus. Pressure on this vein from the cancer can cause the head, arm, and upper chest to turn a bluish-red color. This is known as SVC syndrome, and can affect the brain and threaten the childs life. Children with SVC syndrome need treatment right away.

In addition to the above, non-Hodgkin lymphoma can cause other more general symptoms. These symptoms include fever, chills, or sweating, especially at night. Doctors sometimes call these effects "B symptoms."

Lymphoma in children is sometimes hard to diagnose because enlarged lymph nodes caused by infections are common. Indeed, there is usually no reason to worry unless the lymph nodes are very swollen (more than 1 inch). Even in these cases, the doctor will probably give the child 2 weeks of antibiotics before deciding on further tests. But if the lymph nodes are swelling quickly or the childs health seems to be getting worse, action is needed right away.

How Is Childhood Non-Hodgkin Lymphoma 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.

Before treatment starts, it�s a good idea to talk to the cancer care team about the side effects your child might have. They can tell you about the common side effects, how long they might last, and how serious they might be.

Even if the disease appears to be confined to a single lymph node, it is likely to have spread already. There may be cancer cells in other organs, but these are too small to be felt or seen on imaging tests. This is why surgery and radiation are not commonly used to treat this disease, except to get a better biopsy sample or to relieve a blockage in the child�s intestine.

Radiation can also be used to ease symptoms such as pain caused by the disease. Side effects of radiation treatment can include mild skin problems or tiredness. Treatment to the abdomen can cause upset stomach and diarrhea. Often these effects go away after a short while.

But there can be long-term side effects. Radiation to the chest may cause lung damage and lead to breathing problems. There can also be a higher risk of getting lung cancer or breast cancer (for girls) in later years. If the brain received radiation treatment, side effects such as headaches and trouble thinking could show up 1 or 2 years later. Treatment to the chest could affect the heart and blood vessels. And there is the danger of other cancers (sarcomas) developing later.

Chemotherapy

Chemotherapy is 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. This treatment is useful for cancer that has spread to other organs. For non-Hodgkin lymphoma, a combination of several drugs is given over a period of time. All 3 types of this disease are treated with chemotherapy. The difference is in which drugs are used and for how long they are given.

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

  • hair loss (the hair grows back after treatment ends)
  • diarrhea
  • nausea
  • mouth sores
  • increased chance of infection (from low white blood cell counts)
  • bleeding or bruising after minor cuts or injuries (from a shortage of platelets, cells that help the blood form a clot)
  • fatigue (from low red blood cell counts)

Your child's doctor can often suggest ways to reduce these side effects. Drugs can be given along with chemotherapy to prevent or reduce nausea and vomiting. Drugs known as growth factors can be given to help keep the blood cell counts higher.

Tumor lysis syndrome is a side effect of chemotherapy that results from the rapid breakdown of lymphoma cells. When the cells are destroyed, they release their contents into the bloodstream. This can affect the kidneys, heart, and nervous system. The problem can be prevented by making sure the child gets lots of fluids and giving certain drugs that help the body get rid of these substances.

Organs that can be directly damaged by some chemotherapy include the kidneys, liver, testes, ovaries, brain, heart, and lungs. With careful watching, life-threatening side effects are rare. Sometimes the chemotherapy may have to be reduced or stopped for a while.

One of the most serious side effects of treatment is the possibility of your child getting a second cancer called AML (acute myeloid leukemia). This is quite rare, and the importance of chemotherapy in treating non-Hodgkin lymphoma in children far outweighs the small risk.

Monoclonal antibodies are another form of treatment. They are like antibodies that are made by the immune system, but they are made in the lab. Instead of attacking germs the way natural antibodies do, some monoclonal antibodies are designed to attack lymphoma cells.

After years of research, several monoclonal antibodies are now being used as treatments for lymphoma. In fact, more monoclonal antibodies are available to treat lymphoma than any other type of cancer.

The first monoclonal antibody approved by the FDA to treat any cancer was rituximab (Rituxan). Common side effects are usually mild but may include chills, fever, nausea, rashes, fatigue, and headaches. Even if these problems happen when rituximab is first given, it is very unusual for them to continue. Other monoclonal antibodies to treat lymphomas are also being developed.

Bone Marrow Transplantation (BMT) and Peripheral Stem Cell Transplantation (PBSCT)

These treatments are used for children who relapse during or after treatment. They allow doctors to use higher doses of chemotherapy than would normally be the case. But high doses of chemotherapy drugs destroy the bone marrow, which prevents new blood cells from being formed. This could be life-threatening.

Doctors try to avoid this problem by giving the child blood-forming stem cells after treatment. The stem cells are able to create new bone marrow cells. These stem cells can be taken either from the child and stored before treatment, or they can be donated from another person.

In the first approach (called an autologous transplant), the stem cells are removed from the child�s bone marrow or bloodstream before treatment starts. They are frozen and stored. After treatment with high doses of chemotherapy (and sometimes radiation), the cells are thawed and returned to the child through a vein. This is the most common approach.

The second method (called an allogeneic transplant) uses cells from another person. This may be done when cancer cells are found in the child�s own bone marrow in order to avoid returning cancer cells to the child after treatment.

If the child has a brother or sister who has the same tissue type, their bone marrow cells (or perhaps stem cells from the blood) can be used instead of the child�s own cells. If a parent is a close match to the child, the parent's cells can be used. A matched, unrelated donor might also be used.

These transplant treatments are complex. If the doctor thinks your child might benefit from transplantation, the best place to have it may be in a nationally recognized cancer center or in a hospital associated with a university. The staff there should have experience with the procedure. To learn more about this treatment, please see the ACS document, Bone Marrow and Peripheral Blood Stem Cell Transplants.

Childhood Non-Hodgkin Lymphoma Survival Rates

The five-year survival rate for children younger than 20 years old with non-Hodgkin lymphoma ranges from around 70% to 90%, depending on the exact type of lymphoma. This rate refers to patients who live at least 5 years after the cancer is found. Of course, many patients live much longer than 5 years.

These numbers provide an overall picture, but keep in mind that every persons situation is unique and the numbers can't predict exactly what will happen in your childs case. Talk with your cancer care team if you have questions about your childs chances of a cure. They know your child's situation best.