Population-Level Identification of Patients With Lynch Syndrome for Clinical Care, Quality Improvement, and Research.
Ravi N SharafNatalia UdaltsovaDan LiRish K PaiSoham SinhaZixuan LiDouglas A CorleyPublished in: JCO clinical cancer informatics (2024)
It is feasible to electronically characterize the diagnostic processes of LS. No single data source comprehensively identifies all LS carriers. There is underutilization of LS genetic testing for those eligible and underdiagnosis of LS. Our work informs similar efforts in other settings for hereditary cancer syndromes.