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MUTYH: Options for Managing Cancer Risk

People with a mutation in both copies of their MUTYH gene have options for managing their cancer risk. Learn about the screening and prevention guidelines. Stay up to date by signing up for our community newsletter.
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Risk Management for People with Inherited MUTYH Mutations

MUTYH-associated polyposis (MAP) 

Experts guidelines on risk-management for people with MAP are listed below. Importantly, these risks and interventions do not apply to people who have a mutation in only one copy of their MUTYH gene. See below for the specific risk-management options for people with 1 MUTYH mutation. 

Risk management guidelines for people with MUTYH-associated polyposis (MAP)

Beginning Age

Recommendation

25-30

Annual physical exam.

25-30 (or earlier based on family history)

High-quality colonoscopy.

30-35

Baseline upper endoscopy (frequency of follow-up depends on number, size, and type of polyps found), typically with a specialized scope that can evaluate the ampullar of Vater.

For individuals with a personal history of cancer, and/or a high polyp burden

Consider total colectomy with ileorectal anastomosis, followed by scoping at least once yearly to screen remaining large bowel tissue. See our section on colectomy for a description of this procedure.

No specified age

Speak with your doctor about the benefits and risks of risk-reducing medications.

Source: NCCN Guidelines: Genetic/Familial High-Risk Assessment: Colorectal, Endometrial, and Gastric vs. 1 2024


Screening for people with a mutation in one of their MUTYH genes

For people with a mutation in one copy of their MUTYH gene, NCCN recommends following the same screening guidelines as people who do not have a mutation.  

Last updated January 01, 2024