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Unscreened without CRC s/sx
Life expectancy <5y or with high-risk conditions (eg, neutropenia, unstable angina, or high operative risk) Life expectancy ≥5y without high-risk conditions (eg, neutropenia, unstable angina, or high operative risk) No FHx, no IBD, no confirmed/suspected genetic syndrome (average risk) Screen beginning at age 50 [A] regardless of race1 w/ any of the following strategies:2 Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA3 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography4 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 Rationale for early screening of African Americans is higher age-specific rates of CRC. However, the rationale against early screening includes: • Most CRC cases in African Americans occur after age 60
• Prevalence of polyps >9 mm similar for whites and African Americans
• No evidence supporting effectiveness of early screening
• Increasing screening rates by >10% among African Americans >50 yo more effective than early screening.
Guidelines for initiation of screening of African Americans vary:
• USPSTF, ASC-MSTF-ACR: age 50
• ACG, ASGE: age 45
• ACP: age 40
Coverage varies. Medicare and states w/ mandatory screening requirement: age 50.
2 Screening for Colorectal Cancer: U.S. Preventive Services Task Force Recommendation Statement. JAMA. 2016;315(23):2564-2575. PDF
3 Multi-targeted stool DNA testing
• Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false-positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
4 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
Consider screening on case-by-case basis [C] w/ any of the following strategies regardless of race:1 Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA2 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography3 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 Screening for Colorectal Cancer: U.S. Preventive Services Task Force Recommendation Statement. JAMA. 2016;315(23):2564-2575. PDF
2 Multi-targeted stool DNA testing
• Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false-positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
3 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
Do not screen; risks outweigh benefits [D]
(+)FHx of CRC/adenoma in 1 or more 1st-degree, or CRC in 2 or more 2nd-degree relatives without IBD/genetic syndrome (increased risk) One 1st-degree relative dx with CRC/adenoma ≥60 yo, or 2 or more 2nd-degree relatives with CRC Screen beginning @ age 40 w/ any of the following strategies:1-3 Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA4 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography5 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 Screening and Surveillance for the Early Detection of Colorectal Cancer and Adenomatous Polyps, 2008: A Joint Guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. CA Cancer J Clin. 2008;58(3);130-60. PDF
2 According to expert opinion, these recs apply to relatives w/ advanced adenomas (≥1 cm, villous, or w/ high-grade dysplasia); this info is often not available.
3 Evidence for these guidelines not strong and some aspects controversial.
4 Multi-targeted stool DNA testing
• Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false-positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
5 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
1st–degree relative dx with CRC/adenoma dx <60 yo, or 2 or more 1st-degree relatives with CRC/adenoma dx @ any age Colonoscopy screening q5y beginning @ age 40, or 10y before youngest family member dx, whichever comes first1-3 Footnotes 1 Screening and Surveillance for the Early Detection of Colorectal Cancer and Adenomatous Polyps, 2008: A Joint Guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. CA Cancer J Clin. 2008;58(3);130-60. PDF
2 According to expert opinion, these recs apply to relatives w/ advanced adenomas (≥1 cm, villous, or w/ high-grade dysplasia); this info is often not available.
3 Evidence for these guidelines not strong and some aspects controversial.
IBD without confirmed/suspected genetic syndrome (high risk) Refer to a center w/ experience in IBD surveillance/mgmt
Confirmed/suspected genetic syndrome (highest risk) Refer for genetic counseling/testing for genetic syndromes;1 may begin testing in late teens/20s2 Footnotes 1 FHx of, or suspected, Hereditary Non-Polyposis Colon Cancer (HNPCC), Familial Adenomatous Polyposis (FAP), or other syndrome.
2 FHx must be known early.
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Screened with NL results, without CRC s/sx
Life expectancy <5y or with high-risk conditions (eg, neutropenia, unstable angina, or high operative risk) Life expectancy ≥5y without high-risk conditions (eg, neutropenia, unstable angina, or high operative risk) No FHx, no IBD, no confirmed/suspected genetic syndrome (average risk) Screen w/ any of the following strategies [A] regardless of race:
Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA1 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography2 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 Multi-targeted stool DNA testing • Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false-positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
2 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
If pt has hx of adequate CRC screening, then do not routinely screen as risks may outweigh benefits If no hx of adequate CRC screening, then consider screening on case-by-case basis [C] w/ any of the following strategies: Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA1 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography2 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 Multi-targeted stool DNA testing • Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
2 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
Do not screen; risks outweigh benefits [D]
(+)FHx of CRC/adenoma in one or more 1st-degree, or CRC in 2 or more 2nd-degree relatives without IBD/genetic syndrome (increased risk) One 1st-degree relative dx with CRC/adenoma ≥60 yo, or 2 or more 2nd-degree relatives with CRC Screen w/ any of the following strategies:1 Stool-based tests - Highly sensitive guaiac FOBT (eg, Hemoccult SENSA) annually
- FIT annually
- FIT-DNA2 (Cologuard) annually or q3y
Visualization tests - Colonoscopy q10y
- CT colonography3 q5y
- Flex sig q5y
- Flex sig w/ FIT: flex sig q10y + FIT annually
Footnotes 1 According to expert opinion, these recs apply to relatives w/ advanced adenomas (≥1 cm, villous, or w/ high-grade dysplasia); this info is often not available.
2 Multi-targeted stool DNA testing
• Combines FIT w/ stool DNA test (Cologuard)
• Higher single-test CA and polyp detection vs FIT alone
• Lower specificity than FIT alone, thus more false-positives & more diagnostic colonoscopies
• Insufficient evidence on appropriate f/u of (+) findings after a negative colonoscopy; may lead to overly intense surveillance due to concerns over DNA component
• Medicare reimburse q3y
3 CT Colonography (virtual colonoscopy)
• Requires bowel prep
• Sensitive for polyps ≥6 mm and CA
• Incidental extracolonic findings (ECFs) are common, most do not require additional eval
• ECFs have potential for both benefit (eg, discovery of AAA and extracolonic CA) and harm (over-dx and over-tx), but limited evidence
• Facility should have capability for same-day colonoscopy when needed to remove polyps
• As of July 2016, not covered for screening by Medicare, but coverage being reconsidered (check ACR Website)
• Covered for screening by some private insurers
1st-degree relative dx with CRC/adenoma dx <60 yo, or 2 or more 1st-degree relatives with CRC/adenoma dx @ any age Colonoscopy screening q5y1,2 Footnotes 1 Evaluating Test Strategies for Colorectal Cancer Screening: A Decision Analysis for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;149:659-669. PDF
2 According to expert opinion, these recs apply to relatives w/ advanced adenomas (≥1 cm, villous, or w/ high-grade dysplasia); this info is often not available.
IBD without confirmed/suspected genetic syndrome (high risk) Refer to a center w/ experience in IBD surveillance/mgmt
Confirmed/suspected genetic syndrome (highest risk) Refer for genetic counseling/testing for genetic syndromes;1 may begin testing in late teens/20s2 Footnotes 1 FHx of, or suspected, Hereditary Non-Polyposis Colon Cancer (HNPCC), Familial Adenomatous Polyposis (FAP), or other syndrome.
2 FHx must be known early.
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Abnormal CRC screening results
Abnormal stool test/flex sig/CTC Adenomatous polyp(s) only on colonoscopy 1st surveillance colonoscopy timing based on adenoma size/number/type1,2 (assumes complete, nonpiecemeal excision):3 - If >10 adenomas (high risk; consider syndrome): repeat at <3y
- If <10 adenomas AND at least 3+ are <10 mm or any ≥10 mm or w/ villous features/high-grade dysplasia: repeat at 3y; however, if only 1-2 tubular (low risk) <10 mm, repeat in 5-10y4
Subsequent F/U surveillance: base interval for 2nd surveillance on results of 1st surveillance: Footnotes 1 Guidelines for Colonoscopy Surveillance After Screening and Polypectomy: A Consensus Update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology. 2012;143(3):844-857.
2 These recs assume that prior colonoscopy was complete/adequate.
3 Repeat colonoscopy in 2-6mo if any adenoma w/ piecemeal, or possibly incomplete, excision.
4 For pts w/ high-risk FHx: colonoscopy q5y, IBD and genetic syndromes are referred to a center w/ experience in IBD surveillance/mgmt.
5 Low-risk adenoma: 1-2 tubular adenomas <10 mm.
6 High-risk adenomas include:
• >10 adenomas
• <10 adenomas: if ≥3 all <10 mm or if any ≥10 mm or if any w/ villous features/high-grade dysplasia. Serrated polyp(s) only on colonoscopy 1st surveillance colonoscopy timing based on polyp type/size/location:1-3 - If serrated4 polyposis/formerly hyperplastic polyposis (per WHO definition):5 repeat in 1y
- If serrated4 polyp(s) ≥10 mm or w/ dysplasia: repeat in 3y
- If serrated4 polyp(s) <10 mm w/o dysplasia: repeat in 5y
- If only hyperplastic polyp(s) >5 mm, proximal to sigmoid: repeat in 5y
- If only hyperplastic polyp(s) ≤5 mm, proximal to sigmoid: repeat in 10y6
- If only hyperplastic polyp(s) <10 mm in rectum or sigmoid: repeat in 10y w/ any method6,7
Footnotes 1 Serrated Lesions of the Colorectum: Review and Recommendations From an Expert Panel. Am J Gastroenterol. 2012;107(9):1315-29. PDF
2 The understanding of serrated polyps is evolving; current mgmt guidelines based on weak evidence.
3 IBD and genetic syndromes are referred to a center w/ experience in IBD surveillance/mgmt.
4 Serrated lesions characterized histologically by a serrated (saw-toothed) appearance of crypt epithelium. In the past, most serrated lesions were called hyperplastic polyps and were thought to have no malignant potential. More recently, a subset of serrated lesions has been identified as the precursor of 20%–30% of CRCs, mainly in proximal colon.
5 WHO definition: 1) ≥5 hyperplastic and/or serrated polyps proximal to sigmoid ≥2 of which are >1 cm, OR 2) any # serrated proximal to sigmoid in pt w/ 1st-degree relative w/ serrated polyposis, OR 3) >20 serrated (any size) distributed throughout the colon.
6 10-yr recommendation is only for average-risk pts.
7 F/U interval screening w/ any of the following tests:
• Highly sensitive guaiac FOBT (eg, Hemoccult SENSA)
• FIT
• FIT-DNA (Cologuard)
• Colonoscopy
• CT colonography
• Flex sig
• Flex sig w/ FIT
Adenomatous + serrated polyp(s) on colonoscopy 1st surveillance colonoscopy timing based on recommended interval for most serious lesion (assumes complete, nonpiecemeal excision of adenoma):1-3 - Serrated polyposis/formerly hyperplastic polyposis (per WHO definition):4 repeat in 1y
- >10 adenomas (high risk; consider syndrome): repeat in <3y
- If serrated polyp(s) ≥10 mm or w/ dysplasia or <10 adenomas: if 3+ all <10 mm or any ≥10 mm or w/ villous features/high-grade dysplasia: repeat in 3y
- If serrated polyp(s) <10 mm w/o dysplasia or if only hyperplastic polyp(s) >5 mm, proximal to sigmoid: repeat in 5y
- If 1-2 tubular adenomas + hyperplastic polyp(s) ≤5 mm, proximal to sigmoid or hyperplastic polyp <10 mm in rectum or sigmoid, repeat in 5-10y5
Footnotes 1 Guidelines for Colonoscopy Surveillance After Screening and Polypectomy: A Consensus Update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology. 2012;143(3):844-857. PDF
2 Serrated Lesions of the Colorectum: Review and Recommendations From an Expert Panel. Am J Gastroenterol. 2012;107(9):1315-29. PDF
3 Repeat colonoscopy in 2-6mo if any adenoma w/ piecemeal, or possibly incomplete, excision.
4 WHO definition: 1) ≥5 hyperplastic and/or serrated polyps proximal to sigmoid ≥2 of which are >1 cm, OR 2) any # serrated proximal to sigmoid in pt w/ 1st-degree relative w/ serrated polyposis, OR 3) >20 serrated (any size) distributed throughout the colon.
5 For pts w/ high-risk FHx: colonoscopy q5y, IBD and genetic syndromes are referred to a center w/ experience in IBD surveillance/mgmt.
Colorectal CA, postresection Base surveillance colonoscopy timing on completeness of pre-op eval; if rectal CA, also consider additional surveillance:1 - If incomplete pre-op eval,2 colonoscopy w/in 6mo postresection
- If complete pre-op eval,2 colonoscopy w/in 1y postresection; if 1-yr exam is negative, next colonoscopy @ 3y, then q5y
- Consider additional surveillance for rectal local recurrence w/ flex sig, rigid proctoscope, or rectal U/S q3-6mo x2-3y
Footnotes 1 Colonoscopy Surveillance After Colorectal Cancer Resection: Recommendations of the US Multi-Society Task Force on Colorectal Cancer. Gastrointest Endosc. 2016;83(3)489-98. PDF
2 Every effort should be made to clear colon of synchronous lesions preoperatively using colonoscopy for nonobstructing tumors. For obstructing tumors, use CTC, or if not available, CT or Gastrografin enema.
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