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Colorectal cancer is the second most common cause of cancer
and cancer death in American men and women. Approximately one out of every 18
people will develop colorectal cancer in their lifetime.
Is colorectal cancer preventable?
Unfortunately, half of people who get colon cancer
will have disease that is at an advanced stage. When colorectal cancer is found
at an advanced stage, the chance of cure is much less than when it is detected
early. Fortunately, colorectal cancer is preventable by having regular checks of
the colon called screenings. Colorectal cancer forms from polyps, called
adenomas. If adenomas are found and removed before they grow large and turn into
cancer, cancer is prevented. Even if cancer is found, it is curable in over 90%
of patients if caught early. Most polyps and curable cancers do not produce
symptoms. Therefore, do not wait for symptoms to develop, see your doctor for
colon checks on a regular basis while you are feeling well.
Who is at risk of colorectal cancer?
We are all at risk of developing colorectal cancer.
Over 75% of patients who get colorectal cancer have no identifiable risk
factors. They are a group of patients called average risk. The remainder of
patients either has a personal history of colorectal polyps or cancer,
ulcerative or Crohn's colitis, or a strong family history of colorectal cancer.
These patients are at moderate to high risk. When we say a strong family history
we mean a family that contains multiple relatives or first-degree relatives
(parent, brother/sister, or child) with colorectal cancer. The risk is
particularly strong if the first degree relative with cancer was less than age
50.
Colorectal cancer screening to detect cancers and precancerous
adenomatous polyps in average risk patients is encouraged by at least three
expert groups. All screening options are not acceptable for patients
with symptoms that could be consistent with colorectal cancer or patients at
moderate or high risk. Symptoms of colorectal cancer include a change in bowel
habits, abdominal pain, rectal bleeding or anemia. Patients with symptoms or at
moderate to high risk should have an examination of the whole colon called
colonoscopy.
Average risk:
People with no symptoms or any of the risk factors in
moderate or high-risk group are considered average risk at developing colorectal
cancer. These people should be screened for colorectal cancer starting at age
50.
Recommendations: (Options include either)
Fecal blood testing (FOBT) every year
This is a test on smears of stool. It can detect
microscopic blood by a chemical reaction. Patients should be on a specialized
diet before this test is performed to try to minimize falsely positive or
negative tests. The restrictions include:
- No red meat, poultry,
certain raw vegetables and melons
- No anti-inflammatory
medications or aspirin for 7 days
- No vitamin C (or
multivitamins with vitamin C)
The test is positive if any of six windows change to a blue
color. If it is positive, a colonoscopy should be performed.
Flexible sigmoidoscopy every 5 years
This is a test where a physician passes a thin,
flexible tube into the lower colon and examines the lining. It is done in
addition to the yearly fecal occult blood testing. If an adenoma is found during
the flexible sigmoidoscopy, a colonoscopy should be performed to remove the
polyp and search for polyps higher in the colon. It is recommended that flexible
sigmoidoscopy be combined with an annual FOBT.
Barium enema plus sigmoidoscopy
A barium enema is an x-ray. It is not accurate enough
to check for colorectal polyps and can even miss cancers. It should not be used
for colorectal cancer screening unless a colonoscopy cannot be performed. If it
is used, it should be coupled with a flexible sigmoidoscopy to see the part of
the lower colon that is not well seen on x-ray.
Colonoscopy every 10 years
Colonoscopy is a test where the doctor inserts a thin
flexible tube into the complete colon. If the examination is normal, this test
is done every 10 years. Colonoscopy is the preferred colorectal cancer screening
test. It is also the test of choice if patients have any symptoms that could be
suggestive of colorectal cancer such as intestinal bleeding, unexplained
abdominal pain or change in bowel habits. No additional FOBT or sigmoidoscopy
should be done between colonoscopy examinations. If any polyps are seen during
the exam, they should be removed and sent to the laboratory for analysis. If
adenomas are found, generally follow up colonoscopy is performed in 3 to 5
years. Many patients with adenomas require lifelong colonoscopy at 3 to 5 year
intervals.
Moderate risk:
Those people at moderate risk of developing colorectal
cancer have a personal history of adenomatous polyps or colorectal cancer; one
first degree relative (parent, child or sibling) with colorectal cancer or
adenoma < 50 years of age; or more than 1 first degree relative with
colorectal cancer at any age.
Recommendation:
- Colonoscopy every 5
years
- Start at age 40, or 10
years before the youngest case in the family, whichever is earlier
High risk:
Those people with an inherited predisposition to
colorectal cancer such as familial adenomatous polyposis (FAP) or Hereditary
Nonpolyposis Colorectal Cancer (HNPCC) are considered at high risk for
developing colorectal cancer. They and their family members should be seen by
a team of experts familiar with the diagnosis and treatment of these
disorders.
Familial adenomatous polyposis (FAP)
Recommendation:
- Flexible sigmoidoscopy or
colonoscopy every 6-12 months. Start in puberty
- Refer to Medical Genetics at
(216) 445 5686, the High Risk Clinic and Inherited Colorectal Cancer
Registry at (216) 444-6470
Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
These are families with colorectal cancer in at least
three relatives, one first-degree relative of other two, and occurring over two
generations. At least one relative must be diagnosed with colorectal cancer <
50 years of age. These families may also have uterine, ovarian or other
gastrointestinal or urinary cancers.
Recommendation:
- Colonoscopy every 2 years
until age 40; then every year.
- Start at age 25 or 10 years
younger than the youngest case in the family.
- Pelvic Ultrasound and
endometrial biopsy every year beginning at age 25.
- Refer to Medical Genetics at
(216) 445 5686, the High Risk Clinic and Inherited Colorectal Cancer
Registry at (216) 444-6470
Inflammatory bowel disease (Crohn's or ulcerative colitis)
People with inflammatory bowel disease (IBD) should
have a colonoscopy with biopsy for dysplasia every 1-2 years. Colonoscopies
should start 8 years after the onset of symptoms if the whole colon has been
inflamed (pancolitis) and 12 years after the onset of symptoms if only the
left-side of the colon has been inflamed.
Report of the U.S. Preventive Services Task Force.
Guide to Clinical Preventive Services. Baltimore, MD: Williams &
Wilkins, 1996.
Winawer S, Fletcher R, Rex D, et al. Gastrointestinal
Consortium Panel. Colorectal Cancer Screening and Surveillance: Clinical
Guidelines and Rationale—Update based on new evidence. Gastroenterology
2003;124:544-60.
Smith RA, Cokkinides V, Eyre HJ. American Cancer
Society Guidelines for the Early Detection of Cancer, 2004. Ca: a Cancer
Journal for Clinicians 2004;54(Jan-Feb):41-52.
Ransohoff, DF, Lang CA. Clinical Guideline: Part I and
Part II. Ann Intern Med 1997;126:808-822.
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