brand logo

Am Fam Physician. 2022;105(3):327-329

This clinical content conforms to AAFP criteria for CME.

Author disclosure: No relevant financial relationships.

Key Points for Practice

• Start CRC screening at 50 years of age, but consider offering it at 45 years of age for average-risk patients.

• CRC screening beyond age 75 should be individualized based on life expectancy and risk of adverse events.

• Colonoscopy or FIT is recommended for CRC screening because of cost and clinical effectiveness, but other screening tools can be used based on patient preference.

From the AFP Editors

Colorectal cancer (CRC) is the third most common cancer in the United States and ranks second for cancer-related deaths. Between 2011 and 2016, CRC incidence increased at a rate of 1% per year for individuals at average risk, reversing a continuous decrease between 1980 and 2010. The obesity epidemic appears to be the key driver of recent increases. Early detection through screening, removal of precancerous polyps with colonoscopy, and changes in modifiable risk factors were thought to contribute to previous reductions. The American College of Gastroenterology (ACG) released updated guidelines for CRC screening.

When to Screen

The ACG continues to strongly recommend CRC screening between 50 and 75 years of age, and starting screening at 45 years of age is conditionally recommended. Between 1974 and 2013, CRC incidence increased by 51% in people younger than 50 years. Predictive models suggest an increase of 25 life-years per 1,000 persons when screening starts at age 45, although this evidence is very low quality.

When patients are older than 75 years, the decision to screen should be individualized based on patient life expectancy and adverse outcome risk. The benefit of polyp removal is only seen after seven to 10 years, when other medical concerns may affect health more. Older patients have higher adverse event risks, including perforation during colonoscopy, false-positive results, and electrolyte disturbances and dehydration during bowel preparation.

If patients have a first-degree relative with CRC or advanced polyps before 60 years of age or two first-degree relatives with CRC or advanced polyps after age 60, consider screening at 40 years of age or 10 years younger than the youngest affected relative. Up to 10% of adults have this family history, which at least doubles CRC risk. Commencing screening 10 years before diagnosis is a conditional recommendation because of very low quality evidence. Table 1 reviews screening recommendations.

Risk levelActionAgeStrength of recommendationEvidence grade
Average riskStart screening45 yearsConditionalVery low
Screen50 to 75 yearsStrongModerate
Stop screening> 75 yearsConditionalVery low
One or more first-degree relatives with colon cancer or advanced polypsStart screening40 years or 10 years before age of youngest relative at time of diagnosisConditionalVery low

Screening Modalities and Frequency

The ACG recommends colonoscopy or fecal immunochemical testing (FIT) as the primary CRC screening method because of cost and clinical effectiveness. Several other two-step screening modalities are acceptable if patient preference increases screening.

Colonoscopy is the only one-step CRC screening modality, because it functions as a diagnostic procedure for the entire colon and a therapeutic procedure when polyps are removed. Colonoscopy has near perfect CRC detection accuracy. The use of colonoscopy for screening reduces CRC incidence by 69% and CRC mortality by 68%. Repeat screening after a normal colonoscopy is recommended every 10 years for average-risk patients and every five years for patients who have a first-degree relative with CRC.

Two-step screening methods consist of a screening modality followed by a colonoscopy for a positive test. Flexible sigmoidoscopy enables diagnostic polyp removal up to the distal colon but requires a full colonoscopy after a positive test. Two-step methods require quality assurance programs to ensure that patients with a positive test result receive a follow-up colonoscopy. CRC screening is performed by stool-based tests, blood tests, or direct visualization.

Stool- and blood-based screening does not require bowel preparation before testing. FIT detects CRC with 91% sensitivity and 90% specificity. Although outcome data are lacking, repeated annual FIT leads to an 80% overall CRC detection rate. FIT has largely replaced fecal occult blood testing (FOBT) because of higher sensitivity for detecting CRC and elimination of the dietary or medication modifications required for FOBT. Although the mortality reduction with FIT is unknown, annual FOBT reduces CRC mortality by 33% and biennial FOBT reduces CRC mortality by 18%. The multitarget stool DNA (mtsDNA) test added to FIT every three years detects CRC with 92% sensitivity and 87% specificity. The specificity of mtsDNA decreases with patient age. The reduced specificity of mtsDNA with FIT leads to more colonoscopies, and the follow-up interval after a positive mtsDNA and negative colonoscopy is uncertain. Septin 9 is a U.S. Food and Drug Administration–approved blood test for individuals 50 years and older that detects CRC with 48% sensitivity and 91% specificity. Because of the low sensitivity, the follow-up interval is unknown, and Septin 9 is not recommended by the ACG.

Two-step visualization tests require bowel preparation. Flexible sigmoidoscopy provides direct visualization of the distal colon and has a 90% to 100% sensitivity for CRC in the distal colon. Use of flexible sigmoidoscopy every five to 10 years reduces CRC mortality by 37%. Computed tomographic colonography every five years detects CRC with a sensitivity between 90% and 100%. It has lower sensitivity for polyps, especially flat and sessile serrated lesions. The colon video capsule performed every five years detects polyps of 6 mm or greater with 81% sensitivity and 93% specificity. Table 2 reviews CRC screening modalities and recommended intervals after normal screening.

Already a member/subscriber?  Log In


From $145
  • Immediate, unlimited access to all AFP content
  • More than 130 CME credits/year
  • AAFP app access
  • Print delivery available

Issue Access

  • Immediate, unlimited access to this issue's content
  • CME credits
  • AAFP app access
  • Print delivery available
Purchase Access:  Learn More

Coverage of guidelines from other organizations does not imply endorsement by AFP or the AAFP.

This series is coordinated by Michael J. Arnold, MD, associate medical editor.

A collection of Practice Guidelines published in AFP is available at

Continue Reading

More in AFP

More in Pubmed

Copyright © 2022 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP.  See permissions for copyright questions and/or permission requests.