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| AuthorRobert H Fletcher, MD, MSc | Section EditorKenneth K Tanabe, MD | Deputy EditorsLeah K Moynihan, RNC, MSNH Nancy Sokol, MD |
Contents of this article
COLON CANCER SCREENING OVERVIEW
Colorectal cancer is a cancer that develops in the large intestine [colon] or rectum. The primary goal of colon cancer screening is to prevent deaths from colon cancer. Screening tests can help identify cancers at an early and potentially treatable stage. Some tests can also prevent the development of colorectal cancer by identifying precancerous abnormal growths called adenomatous polyps; these polyps can be removed before they become malignant.
All adults should undergo colon cancer screening beginning at age 50 or earlier, depending upon your risk of developing colorectal cancer. Several tests are currently available, each of which has advantages and disadvantages. The optimal screening test depends upon your preferences and your risk of developing colon cancer.
This article discusses colon cancer risks, available screening tests, and recommendations for screening based upon your risks. There are additional topics about the screening tests themselves (see "Patient information: Flexible sigmoidoscopy" and "Patient information: Colonoscopy") as well as about particular conditions (see "Patient information: Colon polyps" and "Patient information: Crohn's disease" and "Patient information: Ulcerative colitis".
EFFECTIVENESS OF COLON CANCER SCREENING
Most colorectal cancers develop from precancerous adenomatous polyps. A small percentage of these polyps become cancerous and spread to other areas. This progression takes at least 10 years in most people.
Colon cancer screening tests work by detecting polyps or by finding early stage cancers. Regular screening for and removal of polyps can reduce your risk of developing colorectal cancer by up to 90 percent. Early detection of cancers that are already present in the colon increases the chances of successful treatment and decreases the chance of dying as a result of the cancer.
Several factors increase an individual's risk of developing colorectal cancer. Having one or more of these factors will determine the age when you should begin screening, the frequency of screening, and the screening tests that are most appropriate.
Small increases in risk — Several characteristics increase the risk of colorectal cancer. While each individual risk factor adds some risk, risk is substantially increased if several are present together.
Factors that decrease risk — Factors that may decrease risk include:
Large increase in risk — Some conditions greatly increase the risk of colorectal cancer.
Familial adenomatous polyposis — Familial adenomatous polyposis (FAP) is an uncommon inherited condition that increases the risk of colorectal cancer. Nearly 100 percent of people with this condition will develop colorectal cancer during their lifetime, and most of these cancers occur before the age of 50 years. FAP causes hundreds of polyps to develop throughout the colon. (See "Clinical features and diagnosis of familial adenomatous polyposis".)
Hereditary nonpolyposis colon cancer — Hereditary nonpolyposis colon cancer (HNPCC, also called Lynch syndrome) is another inherited condition associated with an increased risk of colorectal cancer. It is slightly more common than FAP, but is still uncommon, accounting for about 1 in 20 cases of colorectal cancer. About 70 percent of people with HNPCC will experience colorectal cancer by the age of 65. Cancer also tends to occur at younger ages. People with HNPCC are also at risk for other types of cancer, including cancer of the uterus, stomach, bladder, kidney, and ovary. (See "Clinical features and diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer)".)
Inflammatory bowel disease — People with Crohn's disease of the colon or ulcerative colitis have an increased risk of colorectal cancer. The amount of increased risk depends upon the amount of inflamed colon and the duration of disease; pancolitis (inflammation of the entire colon) and colitis of 10 years' duration or longer are associated with the greatest risk for colorectal cancer. The risk of colon cancer is not increased in people with irritable bowel disease.
Several tests are available for colorectal cancer screening, including tests that can detect cancers at an early treatable stage (eg, stool tests), and tests that also detect pre-cancerous polyps (adenomas) and can lead to cancer prevention.
Guidelines from expert groups recommend that you and your healthcare provider discuss the available options and choose a testing strategy that makes sense for you. Tests that detect pre-cancerous polyps are generally preferred; these include colonoscopy, CT colonography, flexible sigmoidoscopy, and double contrast barium enema. Stool tests that detect blood or abnormal DNA are another option [1].
Colonoscopy — Colonoscopy allows a physician to see the lining of the rectum and the entire colon (figure 1). (See "Patient information: Colonoscopy".)
CT colonography ("virtual colonoscopy") — Computed tomography colonography (CTC, sometimes called "virtual colonoscopy") is a test that uses a CT scanner to take images of the entire bowel. These images are in two- and three-dimensions, and are reconstructed to allow a radiologist to determine if polyps or cancers are present (picture 1). The major advantages of CTC are that it does not require sedation, it is non-invasive, the entire bowel can be examined, and abnormal areas (adenomas) can be detected about as well as with traditional (optical) colonoscopy.
There are several disadvantages of CTC. Like traditional colonoscopy, CTC requires a bowel prep to clean out the colon. If an abnormal area is found with CTC, a traditional colonoscopy will be needed at a later time to see the area and take a tissue sample (biopsy). CTC may detect abnormalities other than polyps and colorectal cancer. Many of these incidental findings will require further testing. This test may not be covered by health insurance plans in the United States.
Sigmoidoscopy — Sigmoidoscopy allows a physician to directly view the lining of the rectum and the lower part of the colon (the descending colon, (figure 1). This area accounts for about one-half of the total area of the rectum and colon. (See "Patient information: Flexible sigmoidoscopy".)
Double contrast barium enema — A barium enema test provides a detailed x-ray picture of the rectum and the entire colon (figure 1). This test has largely been replaced by other options. Polyps or cancers cannot be removed during a barium enema, and CT colonography is more accurate for detecting abnormalities [4].
Stool tests — Colorectal cancers often bleed, releasing microscopic amounts of blood and abnormal DNA into the stool. Stool tests can detect blood or abnormal DNA makers.
Two types of tests, called guaiac tests (typically Hemoccult®) and immunochemical tests, evaluate the stool for blood, which may be present if there is bleeding from a colon cancer (or other source of blood).
Fecal occult blood test and sigmoidoscopy — Combined screening with a fecal occult blood test (guaiac) and sigmoidoscopy is a possible screening strategy and may be more effective than either test done alone.
The recommended colon cancer screening plan depends upon your risk of colorectal cancer.
Average risk of colorectal cancer — People with an average risk of colorectal cancer should begin screening at age 50. The following screening strategies are recommended [1]:
Stool testing is an alternate option and is recommended once per year (for guaiac and immunologic tests, less frequently for DNA-based tests). Testing should begin at age 50.
Increased risk of colorectal cancer — Screening plans for people with an increased risk may entail screening at a younger age, more frequent screening, and/or the use of more sensitive screening tests (usually colonoscopy). The optimal screening plan depends upon the reason for increased risk.
Family history of colorectal cancer
Familial adenomatous polyposis — People with a family history of familial adenomatous polyposis (FAP) should consider genetic counseling and genetic testing to determine if they carry the affected gene. People who carry the gene or do not know if they carry the gene should begin screening with sigmoidoscopy once every year, beginning at puberty. (See "Screening and management strategies for patients and families with familial colon cancer syndromes".)
Colectomy (surgical removal of the colon) should be considered if you have multiple polyps or genetic testing shows that you carry the abnormal gene; colectomy is the only way to prevent colorectal cancer in people with FAP.
Hereditary nonpolyposis colon cancer — People with a family history of hereditary nonpolyposis colon cancer (HNPCC) should consider genetic counseling and genetic testing to determine if they carry the affected gene. People who carry the gene or who do not know if they carry the gene should be screened with colonoscopy because HNPCC is associated with cancers of the right-sided colon (which cannot be seen during sigmoidoscopy).
Depending upon your family history and what is found, colonoscopy is usually repeated every one to two years between age 20 and 30 years, and every year after age 40. Because polyps can progress more rapidly to cancer in people with HNPCC, more frequent screening may be recommended. (See "Screening and management strategies for patients and families with familial colon cancer syndromes".)
Inflammatory bowel disease — In people with ulcerative colitis or Crohn's disease of the colon, the optimal screening plan depends upon the amount of colon affected and the duration of the disease. (See "Patient information: Crohn's disease" and "Patient information: Ulcerative colitis" and "Colorectal cancer surveillance in inflammatory bowel disease".)
Your healthcare provider is the best source of information for questions and concerns related to your medical problem. Because no two people are exactly alike and recommendations can vary from one person to another, it is important to seek guidance from a provider who is familiar with your individual situation.
This discussion will be updated as needed every four months on our web site (www.uptodate.com/patients). Additional topics as well as selected discussions written for healthcare professionals are also available for those who would like more detailed information.
Some of the most pertinent include:
Patient Level Information:
Patient information: Flexible sigmoidoscopy
Patient information: Colonoscopy
Patient information: Colon polyps
Patient information: Crohn's disease
Patient information: Ulcerative colitis
Patient information: Colon and rectal cancer
Professional Level Information:
Colorectal cancer surveillance in inflammatory bowel disease
Computed tomographic colonography
Gardner's syndrome
Screening for colorectal cancer: Strategies in patients at average risk
Screening for colorectal cancer: Strategies in patients with possible increased risk due to family history
Clinical features and diagnosis of familial adenomatous polyposis
Clinical features and diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer)
Screening and management strategies for patients and families with familial colon cancer syndromes
A number of web sites have information about medical problems and treatments, although it can be difficult to know which sites are reputable. Information provided by the National Institutes of Health, national medical societies and some other well-established organizations are often reliable sources of information, although the frequency with which they are updated is variable.
1-800-4-CANCER
(www.nci.nih.gov)
(www.cancer.net/portal/site/patient)
1-800-ACS-2345
(www.cancer.org)
(www.nlm.nih.gov/medlineplus/healthtopics.html)
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UpToDate performs a continuous review of over 430 journals and other resources. Updates are added as important new information is published. The literature review for version 17.3 is current through September 2009; this topic was last changed on May 22, 2008. The next version of UpToDate (18.1) will be released in March 2010.
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