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PMID: 42148023 已发表 · epublish 英语

Rectifying referrals: genetics testing is underutilized in rectal cancer patient care.

Proceedings (Baylor University. Medical Center) ·第 39 卷 ·第 3 期

Yu IS, Dao D, Ogola GO, Waddimba AC, Gaidarski AA, Fleshman JW, Lichliter WE, Wells KO

摘要

The National Comprehensive Cancer Network recommends microsatellite instability (MSI)/mismatch repair (MMR) testing to guide genetic counseling referrals for Lynch syndrome (LS) in patients with colorectal cancer. Studies show poor adherence with genetic counseling referral guidelines. Colon and rectal cancers are frequently treated as one entity despite molecular, epidemiologic, and biologic differences. We investigated facility- and patient-level adherence with genetics testing/referral guidelines for LS and other germline mutations among rectal cancer patients at one institution. This is a retrospective review of patients with rectal cancer at a tertiary hospital from 2018 to 2023, excluding years 2020 to 2022 to minimize confounding factors associated with COVID-19. Indications for genetic testing/referrals were based on the Collaborative Group of the Americas on Inherited Colorectal Cancer guidelines. We sampled 177 patients, aged 27 to 96 years. A total of 149 (84.2%) underwent MMR/MSI testing; 47 (26.6%) were eligible for genetics referral. Nineteen (40.4%) were referred to genetics, and 14 (73.7%) underwent counseling/testing. One patient was diagnosed with LS, two with MUTYH-associated polyposis, and one with BRCA2. This study demonstrates poor facility-level adherence with MSI/MMR testing recommendations and poor patient-level compliance with genetic referrals in rectal cancer. When recommendations were met, patients with germline mutations benefited from adjustments to their disease management.

关键词
Colorectal cancer Lynch syndrome genetics germline mutations hereditary cancer syndrome
文献信息
期刊
Proceedings (Baylor University. Medical Center)
期刊简称
Proc (Bayl Univ Med Cent)
ISSN
1525-3252
语言
英语
国家/地区
United States
NLM ID
9302033
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