sábado, 30 de julio de 2016

Tests to Detect Colorectal Cancer and Polyps - National Cancer Institute

Tests to Detect Colorectal Cancer and Polyps - National Cancer Institute

National Cancer Institute

Updated Colorectal Cancer Screening Fact Sheet

Our fact sheet on Tests to Detect Colorectal Cancer and Polyps has been revised to reflect the latest recommendations from the U.S. Preventive Services Task Force and includes an updated list of screening tests.

National Cancer Institute

Tests to Detect Colorectal Cancer and Polyps

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What is colorectal cancer?

Colorectal cancer is a disease in which abnormal cells in the colon or rectum divide uncontrollably, ultimately forming a malignant tumor. (The colon and rectum are parts of the body’s digestive system, which takes up nutrients from food and water and stores solid waste until it passes out of the body.)
Parts of the colon; drawing shows the ascending colon, cecum, transverse colon, descending colon, sigmoid colon, and rectum.
Parts of the colon. Drawing of the front of the abdomen that shows the four sections of the colon: the ascending colon, the transverse colon, the descending colon, and the sigmoid colon. Also shown are the small intestine, the cecum, and the rectum. The cecum, colon, rectum, and anal canal make up the large intestine. The cecum, ascending colon, and transverse colon make up the upper, or proximal, colon; the descending colon and sigmoid colon make up the lower, or distal, colon.
Most colorectal cancers begin as a polyp, a growth in the tissue that lines the inner surface of the colon or rectum. Polyps may be flat, or they may be raised. Raised polyps may grow on the inner surface of the colon or rectum like mushrooms without a stalk (sessile polyps), or they may grow like a mushroom with a stalk (pedunculated polyps).  Polyps are common in people older than 50 years of age, and most are not cancer. However, a certain type of polyp known as an adenoma may have a higher risk of becoming a cancer.
Colorectal cancer is the third most common type of non-skin cancer in both men (afterprostate cancer and lung cancer) and women (after breast cancer and lung cancer). It is the second leading cause of cancer death in the United States after lung cancer. In 2016, an estimated 134,490 people in the United States will be diagnosed with colorectal cancer and 49,190 people will die from it (1).
The rates of new colorectal cancer cases and deaths among adults aged 50 years or older are decreasing in this country due to an increase in screening and to changes in some risk factors (for example, a decline in smoking). However, incidence is increasing among younger adults (1) for reasons that are not known. For example, researchers predict that by 2030, based on current U.S. trends, colon cancer incidence rates will increase by 90% for people aged 20 to 34 years and by 28% for people aged 35 to 49 years, whereas they will decrease by 38% for people aged 50 to 74 years and by 45% for those 75 years or older (2).
The major risk factors for colorectal cancer are a family history of the disease and older age, but several other factors have been associated with increased risk, including excessive alcohol use, obesity, being physically inactive, cigarette smoking, and, possibly, diet.
In addition, people with a history of inflammatory bowel disease (such as ulcerative colitisor Crohn disease) have a higher risk of colorectal cancer than people without such conditions. And people who have certain inherited conditions (such as Lynch syndromeand familial adenomatous polyposis) also have an increased risk of colorectal cancer. 
Several screening tests have been developed to help doctors find colorectal cancer early, when it may be more treatable. Some tests that detect adenomas and polyps can actually prevent the development of cancer because these tests allow growths that might otherwise become cancer to be detected and removed. That is, colorectal cancer screening may be a form of cancer prevention, not just early detection.

What methods are used to screen people for colorectal cancer?

Expert medical groups, including the U.S. Preventive Services Task Force (USPSTF; 3), strongly recommend screening for colorectal cancer. Although minor details of the recommendations may vary, these groups generally recommend that people at average risk of colorectal cancer get screened at regular intervals beginning at age 50 years (3). The USPSTF recommends that screening continue to age 75 years; after age 75, the decision to screen is based on patient’s life expectancy, health status, comorbid conditions, and prior screening results. Routine screening of people aged 86 years or older is not recommended by the USPSTF.
People at increased risk because of a family history of colorectal cancer or polyps or because they have inflammatory bowel disease or certain inherited conditions may be advised to start screening before age 50 and/or have more frequent screening.
The USPSTF considers the following methods to be acceptable screening tests for colorectal cancer:
  • High-sensitivity fecal occult blood tests (FOBT). Both polyps and colorectal cancers can bleed, and FOBT checks for tiny amounts of blood in feces (stool) that cannot be seen visually. (Blood in stool may also indicate the presence of conditions that are not cancer, such as hemorrhoids.)
    Currently, two types of FOBT are approved by the Food and Drug Administration (FDA) to screen for colorectal cancer: guaiac FOBT (gFOBT) and the fecal immunochemical (or immunohistochemical) test (FIT, also known as iFOBT). With both types of FOBT, stool samples are collected by the patient using a kit, and the samples are returned to the doctor.
    • Guaiac FOBT uses a chemical to detect heme, a component of the blood proteinhemoglobin. Because the guaiac FOBT can also detect heme in some foods (for example, red meat), people have to avoid certain foods before having this test.
    • FIT uses antibodies to detect human hemoglobin protein specifically (45). Dietary restrictions are typically not required for FIT.  
    Studies have shown that guaiac FOBT, when performed every 1 to 2 years in people aged 50 to 80 years, can help reduce the number of deaths due to colorectal cancer by 15 to 33% (45). If FOBT is the only type of colorectal cancer screening test performed, experts generally recommend yearly testing.
  • Stool DNA test (FIT-DNA). The only stool DNA test approved by the FDA to date, Cologuard®, is a multitarget test that detects tiny amounts of blood in stool (with an immunochemical test similar to FIT) as well as nine DNA biomarkers in three genes that have been found in colorectal cancer and precancerous advanced adenomas. The DNA comes from cells in the lining of the colon and rectum that are shed and collect in stool as it passes through the large intestine and rectum.  As with both types of FOBT, the stool sample for the FIT-DNA test is collected by the patient using a kit; the sample is mailed to a laboratory for testing. A computer program analyzes the results of the two tests (blood and DNA biomarkers) and provides a finding of negative or positive. People who have a positive finding with this test are advised to have a colonoscopy.
    In one study of people who were at average risk of developing colon cancer and had no symptoms of colon problems (6), this test detected more cancers and adenomas than the FIT test (that is, it was more sensitive). However, the FIT-DNA test also was more likely to identify an abnormality when none was actually present (that is, it had morefalse-positive results). 
  • Sigmoidoscopy. In this test, the rectum and sigmoid colon are examined using asigmoidoscope, a flexible lighted tube with a lens for viewing and a tool for removing tissue. This instrument is inserted through the anus into the rectum and sigmoid colon as air (or carbon dioxide) is pumped into the colon to expand it so the doctor can see the colon lining more clearly. During sigmoidoscopy, abnormal growths in the rectum and sigmoid colon can be removed for analysis (biopsied). The lower colon must be cleared of stool before sigmoidoscopy, but the preparation is less extensive than that required for colonoscopy. People are usually not sedated for this test.
    Studies have shown that people who have regular screening with sigmoidoscopy after age 50 years have a 60 to 70% lower risk of death due to cancer of the rectum and lower colon than people who do not have screening (78). One randomized controlled clinical trial found that even just one sigmoidoscopy screening between 55 and 64 years of age can substantially reduce colorectal cancer incidence and mortality (9). Experts generally recommend sigmoidoscopy every 5 years with or without gFOBT or FIT every 3 years for people at average risk who have had negative test results.
  • Standard (or optical) colonoscopy. In this test, the rectum and entire colon are examined using a colonoscope, a flexible lighted tube with a lens for viewing and a tool for removing tissue. Like the shorter sigmoidoscope, the colonoscope is inserted through the anus into the rectum and the colon as air (or carbon dioxide) is pumped into the colon to expand it so the doctor can see the colon lining more clearly. During colonoscopy, any abnormal growths in the colon and the rectum can be removed, including growths in the upper parts of the colon that are not reached by sigmoidoscopy. A thorough cleansing of the entire colon is necessary before this test. Most patients receive some form of sedation during the test.
    Studies suggest that colonoscopy reduces deaths from colorectal cancer by about 60 to 70%. Additional studies are currently being done to better evaluate how effective colonoscopy screening methods are (10). Experts recommend colonoscopy every 10 years for people at average risk as long as their test results are negative.
  • Virtual colonoscopy. This screening method, also called computed tomographic (CT) colonography, uses special x-ray equipment (a CT scanner) to produce a series of pictures of the colon and the rectum from outside the body. A computer then assembles these pictures into detailed images that can show polyps and other abnormalities. Virtual colonoscopy is less invasive than standard colonoscopy and does not require sedation. As with standard colonoscopy, a thorough cleansing of the colon is necessary before this test, and air (or carbon dioxide) is pumped into the colon to expand it for better viewing of the colon’s lining. The accuracy of virtual colonoscopy is similar to that of standard colonoscopy, and virtual colonoscopy has a lower risk ofcomplications. However, if polyps or other abnormal growths are found during a virtual colonoscopy, a standard colonoscopy is usually performed to remove them.
    Whether virtual colonoscopy can help reduce deaths from colorectal cancer is not yet known, and Medicare and some insurance companies currently do not pay for the costs of this procedure. Studies are ongoing to compare virtual colonoscopy with other screening methods.
  • Other methods. Several other tests to screen for colorectal cancer exist, although these are not generally recommended.
    Double-contrast barium enema. This test, also called DCBE, is another method of visualizing the colon from outside the body. In DCBE, a series of x-ray images of the entire colon and rectum is taken after the patient is given an enema with a barium solution. The barium helps to outline the colon and the rectum on the images. DCBE is rarely used for screening because it is less sensitive than colonoscopy in detecting small polyps and cancers. However, it may be used for people who cannot undergo standard colonoscopy—for example, because they are at particular risk for complications.
    Single-specimen guaiac FOBT done in a doctor's office. Doctors sometimes perform a single-specimen guaiac FOBT on a stool sample collected during a digital rectal examination as part of a routine physical examination. However, this approach has not been shown to be an effective way to screen for colorectal cancer (11).

How can people and their health care providers decide which colorectal cancer screening test(s) to use? 

People should talk with their health care provider about when to begin screening forcolorectal cancer, what test(s) to have, the advantages and disadvantages of each test, how often to undergo screening, and when to stop.
The decision about which test to have usually takes into account several factors, including:
  • The person’s age, medical historyfamily history, and general health
  • The potential harms of the test
  • The preparation required for the test
  • Whether sedation may be needed for the test
  • The follow-up care needed after the test
  • The convenience of the test
  • The cost of the test and the availability of insurance coverage
Colorectal cancer screening tests all have advantages and disadvantages:
  • No cleansing of the colon is necessary.
  • No dietary restrictions are needed before FIT.
  • Samples can be collected at home.
  • Cost is low compared with other colorectal cancer screening tests.
  • There is no risk of damage to the lining of the colon.
  • No sedation is needed.
  • The test does not detect some polyps and cancers.
  • False-positive test results are possible (that is, the test may suggest an abnormality when none is present).
  • Dietary restrictions are needed before guaiac FOBT.
  • Additional procedures, such as colonoscopy, may be needed if the test result shows blood in the stool.
Stool DNA Test (FIT-DNA)
  • No cleansing of the colon is necessary.
  • No dietary restrictions are needed before the test.
  • Samples can be collected at home.
  • There is no risk of damage to the lining of the colon.
  • No sedation is needed.
  • Cost may be higher than that of gFOBT or FIT.
  • Test sensitivity for adenomas is low.
  • False-positive test results are possible (that is, the test may suggest an abnormality when none is present).
  • Additional procedures, such as colonoscopy, may be needed if the test result is positive for blood or abnormal DNA.
  • For most patients, discomfort is minimal, and complications are rare.
  • The doctor can perform a biopsy or polypectomy (removal of a polyp or adenoma) during the test, if necessary.
  • Less extensive cleansing of the colon is necessary for this test than for a colonoscopy.
  • Sedation is often not required.
  • Abnormal growths in the upper part of the colon will be missed because the test allows the doctor to view only the rectum and the lower part of the colon.
  • Bowel cleansing is needed before the test.
  • Medication and diet changes may be needed before the test.
  • There is a very small risk of bleeding or of tearing or perforation of the lining of the colon.
  • Additional procedures, such as colonoscopy, may be needed if the test finds an abnormality.
  • The availability of sigmoidoscopy has decreased substantially in the United States in recent years (12).
Standard Colonoscopy
  • This test is one of the most sensitive currently available.
  • It allows the doctor to view the rectum and the entire colon.
  • The doctor can perform a biopsy or polypectomy during the test if necessary.
  • Even though this test is highly sensitive, it still may not detect all small polyps, flat or depressed (nonpolypoid) lesions, or cancers.
  • A thorough cleansing of the colon is required before the test.
  • Diet changes are needed before the test, and medications may need to be adjusted.
  • Some form of sedation is almost always used. As a result, the patient must have someone accompany them to the procedure and drive them home afterward, and they may not be able to work the day of the procedure.
  • There is a small risk of bleeding or of tearing or perforation of the lining of the colon; this risk increases with age, with the presence of other health problems, and when polyps are removed.
  • With this minimally invasive procedure there is little risk of damage to the lining of the colon.
  • No sedation is needed.
  • A thorough cleansing of the colon is required before the test.
  • Can miss small polyps.
  • Additional procedures, such as colonoscopy, may be needed if the test finds an abnormality.
  • Patient is exposed to small amounts of ionizing radiation.
  • Not covered by all health insurance plans or Medicare.
  • Can unintentionally discover medical results outside the colon that may trigger unnecessary procedures or follow-up.

Does health insurance pay for colorectal cancer screening?

The Affordable Care Act requires coverage of colorectal cancer screening tests by health plans that started on or after September 23, 2010. (For health plans that started before September 23, 2010, the rules about insurance coverage are covered by state laws, which vary, and by other federal laws.) People should check with their health insurance provider to determine their colorectal cancer screening coverage. Medicare covers several colorectal cancer screening tests for its beneficiaries. Specific information about Medicare benefits for colorectal cancer screening is available on the Medicare website.

What happens if a colorectal cancer screening test finds an abnormality?

If a screening test finds an abnormality, additional tests may be recommended. These tests may include x-rays of the gastrointestinal tract, a sigmoidoscopy, or, most often, acolonoscopy if it has not already been done.  If a polyp or tumor is found during a sigmoidoscopy, a biopsy or polypectomy may be performed during the test, and a colonoscopy may be recommended. If a polyp or tumor is found during a standard colonoscopy, a biopsy or polypectomy may be performed during the test to determine whether cancer is present. If a polyp or tumor is detected during virtual colonoscopy, the patient will be referred for a standard colonoscopy.

What new tests are being developed for colorectal cancer screening?

Colorectal polyps and tumors can release cells and DNA into the bloodstream as well as into stool (13). Researchers have found that the presence of an altered gene called SEPT9 in blood can be used to screen for early-stage colorectal cancer and advanced adenomas(14). In clinical studies, a biomarker test that detects altered SEPT9 DNA in blood was no less sensitive than FIT, but it was less specific (15). In April 2016, the FDA approved this as the first blood-based test to screen for colorectal cancer based on its test characteristics. There is no evidence yet that this test can reduce deaths from colorectal cancer.
New approaches to visualize the colon that avoid the need for thorough cleansing of the colon that is currently required for virtual colonoscopy are being studied and refined. One approach is "fecal tagging" with a contrast agent that is ingested over several days before the procedure. This technique allows fecal material in the colon to be differentiated from colon tissue (16); computer software can be used to electronically remove the tagged fecal material from images (17).
Information about ongoing clinical trials that are studying methods for colorectal cancer screening can be found in NCI's clinical trials database. You may also contact NCI’s Cancer Information Service at 1–800–4–CANCER (1–800–422–6237) for assistance with searching the clinical trials database or for other cancer information needs.
Selected References
  1. Howlader N, Noone AM, Krapcho M, et al (eds). SEER Cancer Statistics Review, 1975-2013, National Cancer Institute. Bethesda, MD, http://seer.cancer.gov/csr/1975_2013/, based on November 2015 SEER data submission, posted to the SEER web site, April 2016.
  2. Bailey CE, Hu CY, You YN, et al. Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010. JAMA Surgery 2015; 150(1):17-22.
     [PubMed Abstract]
  3. US Preventive Services Task Force. Screening for colorectal cancer: US Preventive Services Task Force Recommendation Statement. JAMA 2016; 315(23):2564-75.
    [PubMed Abstract]
  4. Burch JA, Soares-Weiser K, St John DJ, et al. Diagnostic accuracy of faecal occult blood tests used in screening for colorectal cancer: A systematic review. Journal of Medical Screening 2007; 14(3):132-137.
     [PubMed Abstract]
  5. Ouyang DL, Chen JJ, Getzenberg RH, Schoen RE. Noninvasive testing for colorectal cancer: A review. American Journal of Gastroenterology 2005; 100(6):1393-1403.
    [PubMed Abstract]
  6. Imperiale TF, Ransohoff DF, Itzkowitz SH, et al. Fecal DNA versus fecal occult blood for colorectal-cancer screening in an average-risk population. New England Journal of Medicine 2004; 351(26):2704-2714.
     [PubMed Abstract]
  7. Elmunzer BJ, Hayward RA, Schoenfeld PS, et al. Effect of flexible sigmoidoscopy-based screening on incidence and mortality of colorectal cancer: A systematic review and meta-analysis of randomized controlled trials. PLoS Medicine 2012; 9(12):e1001352.
    [PubMed Abstract]
  8. Schoen RE, Pinsky PF, Weissfeld JL, et al. Colorectal-cancer incidence and mortality with screening flexible sigmoidoscopy. New England Journal of Medicine 2012; 366(25):2345-2357.
     [PubMed Abstract]
  9. Atkin WS, Edwards R, Kralj-Hans I, et al. Once-only flexible sigmoidoscopy screening in prevention of colorectal cancer: a multicentre randomised controlled trial. Lancet2010; 375(9726):1624-1633.
     [PubMed Abstract]
  10. Ransohoff DF. How much does colonoscopy reduce colon cancer mortality? Annals of Internal Medicine 2009; 150(1):50-52.
  11. Collins JF, Lieberman DA, Durbin TE, Weiss DG; Veterans Affairs Cooperative Study #380 Group. Accuracy of screening for fecal occult blood on a single stool sample obtained by digital rectal examination: A comparison with recommended sampling practice. Annals of Internal Medicine 2005; 142(2):81-85.
     [PubMed Abstract]
  12. Zapka J, Klabunde CN, Taplin S, et al. Screening colonoscopy in the US: Attitudes and practices of primary care physicians. Journal of General Internal Medicine 2012; 27(9):1150-1158.
     [PubMed Abstract]
  13. Mead R, Duku M, Bhandari P, Cree IA. Circulating tumour markers can define patients with normal colons, benign polyps, and cancers. British Journal of Cancer 2011; 105(2):239-245.
     [PubMed Abstract]
  14. Church TR, Wandell M, Lofton-Day C, et al. Prospective evaluation of methylated SEPT9 in plasma for detection of asymptomatic colorectal cancer. Gut 2014; 63(2):317-325.
    [PubMed Abstract]
  15. Johnson DA, Barclay RL, Mergener K, et al. Plasma Septin9 versus fecal immunochemical testing for colorectal cancer screening: a prospective multicenter study. PLoS One 2014; 9(6):e98238.
     [PubMed Abstract]
  16. Iannaccone R, Laghi A, Catalano C, et al. Computed tomographic colonography without cathartic preparation for the detection of colorectal polyps. Gastroenterology2004; 127(5):1300-1311.
     [PubMed Abstract]
  17. Zalis ME, Blake MA, Cai W, et al. Diagnostic accuracy of laxative-free computed tomographic colonography for detection of adenomatous polyps in asymptomatic adults: A prospective evaluation. Annals of Internal Medicine 2012; 156(10):692-702.
    [PubMed Abstract]
  • Reviewed: July 7, 2016

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