What Is Colon Cancer Genetic Testing?
Colon cancer genetic testing is a blood test that can tell you
whether you carry rare changed, or mutated,
genes that can cause
colon cancer. Although most people who get colon
cancer do not have one of these mutated genes, having them greatly increases
your chance of getting colon cancer.
Colon cancer develops in the
large intestine
when cells change and grow out of control. Colon cancer is
also called colorectal cancer because it can occur in both the colon and in the
lowest section of the colon, which is called the rectum.
Colon
cancer almost always begins as small growths on the inner wall of the colon
called
polyps. A doctor can find and remove polyps during a
colonoscopy, a test in which a doctor uses a flexible
video camera or scope to look at the inside of the colon. If a close member of
your family, such as your brother, sister, or parent, has had colon cancer,
talk with your doctor about colonoscopy screening.
The most common
genetic changes related to colon cancer are familial adenomatous polyposis
(FAP) and hereditary nonpolyposis colorectal cancer (HNPCC). In these
conditions, screening often starts even sooner than age 40.
Familial adenomatous polyposis (FAP)
FAP develops because of a changed gene that causes
hundreds or thousands of polyps to grow in the colon. The number of polyps
increases with age. If one of your parents has FAP, you have a 50% chance of
having the changed gene and the disease.
People with FAP have an
almost 100% chance of getting colorectal cancer.1, 2 They can develop polyps in their
20s and 30s, or even earlier. People with FAP may decide to have their colons
removed to prevent colon cancer.
Hereditary nonpolyposis colorectal cancer (HNPCC) or Lynch syndrome
HNPCC can cause polyps in the colon, but not as many
as FAP. Changes in any of four or more different genes can cause HNPCC. These
changes also increase the risk for other cancers, including cancer of the
endometrium, ovaries, and other organs.
Having HNPCC does not mean
you definitely will develop colon cancer, but it does increase your chances. If
you have one parent who has HNPCC, you have a 50% chance of having one or more
of these gene changes. If both parents have it, your chances of getting it are
about 80%. (Not every person with the genes will get the condition, and not
everyone with the condition will have the abnormal gene.)
If you have a strong family history of colon cancer,
you may want to have a blood test to look for changed genes. You have a strong
family history if:
- You have at least three relatives who have had
colon cancer, and at least one of them is a parent, brother, or sister.
- Those relatives are spread over two generations in a row (for
example, a grandparent and a parent).
- One of those relatives got
cancer before age 50.
Testing is more reliable when the family member who has
colon cancer, FAP, or HNPCC also tests positive for the abnormal gene.
What Do the Results Mean?
Colon cancer genetic
testing is a blood test that looks for the changed (mutated) genes that cause
colon cancer. Although most people who get colon cancer do not have one of
these mutated genes, having them greatly increases your chance of getting colon
cancer.
A positive result means that you may have one of the
changed genes that causes FAP or HNPCC. It also means that your chances of
getting colon cancer are very high. A negative result means that none of these
genes were found in your blood sample.
How Accurate Is the Test?
Although these blood tests
are highly reliable, no test is 100% accurate. The test cannot tell you when or
whether you will develop colon cancer. Testing negative for an inherited colon
cancer gene does not mean you will never get colon cancer. It means your risk
of colon cancer is about the same as that of the average person.
There are many different genetic mutations that can lead to FAP or HNPCC.
Genetic testing does not find all of them. Because of this, a person may have a
normal genetic test but still have an increased chance of having an inherited
colon cancer.
Should I Be Tested?
The decision to be tested for
genetic colon cancer is personal. You may have emotional, financial, and family
reasons for taking or not taking the test.
You might choose to be
tested because:
- You have received
genetic counseling, understand the risks and benefits
of testing, and feel that the benefits outweigh the risks. A
genetic counselor can help you make well-informed
decisions.
- You have a personal history of more than 20 colon
polyps, especially at a young age.
- You have a parent, brother, or
sister who has colon cancer, FAP, or HNPCC and they have tested positive for
the abnormal gene.
- You would be worried not knowing whether you
have an increased chance of getting cancer.
- You plan to make
different medical decisions if you find out your test is positive.
- You would change your decision about having children because of
test results.
Why Would I Not Be Tested?
You might choose not to
be tested because:
- No one in your family has had colon cancer,
FAP, or HNPCC.
- Other people in your family have had colon cancer
but you have regular screening.
- You would worry too much if you
knew you had an increased chance of getting colon cancer.
- You would
not change your decision about having children because of test
results.
- Your health insurance would not pay for the test.
What Is Genetic Counseling?
Information from genetic
testing can have a profound impact on your life. Genetic counselors are trained
to explain the test and its results, but you make the decision about whether to
have the test. A genetic counselor can help you make well informed decisions.
Ask to have genetic counseling before making a decision about testing. Genetic
counseling can help you and your family:
- Understand medical facts, including what causes diseases, how a
diagnosis is made, and what you may be able to do to help you manage a
disease.
- Understand how your family history contributes to the
development of a disease.
- Understand what you can do to help
prevent colon cancer or a recurrence.
- Learn about caring for a
family member with a genetic disease, including getting referrals to
specialists or joining support groups.
Genetic counselors are trained to help you and your family
make informed decisions. They are sensitive to the physical and emotional
aspects of these decisions. Your privacy and confidentiality are carefully
protected.
References
Citations
National Cancer Institute (2006). Genetics of Colorectal Cancer. Available online: http://www.cancer.gov/cancertopics/pdq/genetics/colorectal/healthprofessional.
Winawer S, et al. (2003).
Colorectal cancer screening and surveillance: Clinical guidelines and
rationale-Update based on new evidence. Gastroenterology, 124(2): 544-560.
Other Works Consulted
Chaganti RSK (2008). Genetics of cancer. In L Goldman,
D Ausiello, eds., Cecil Medicine, 23rd ed., pp.
1340-1344. Philadelphia: Saunders Elsevier.
National Cancer Institute (2006). Genetics of Colorectal Cancer. Available online: http://www.cancer.gov/cancertopics/pdq/genetics/colorectal/healthprofessional.
Schroy PC (2006). Screening and surveillance
guidelines for individuals at increased risk section of Neoplastic diseases of
the small and large bowel. In MM Wolfe et al., eds., Therapy of Digestive Disorders, 2nd ed., pp. 890-910. Philadelphia: Saunders
Elsevier.
Seashore MR (2008). Genetic risk assessment. In L
Goldman, D Ausiello, eds., Cecil Medicine, 23rd ed., pp.
216-223. Philadelphia: Saunders Elsevier.
Credits
| Author | Bets Davis, MFA |
| Editor | Maria Essig |
| Associate Editor | Tracy Landauer |
| Primary Medical Reviewer | Anne C. Poinier, MD - Internal Medicine |
| Specialist Medical Reviewer | Siobhan M. Dolan, MD, MPH - Reproductive Genetics |
| Last Updated | May 28, 2008 |