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Article

Feasibility of using patient navigation to improve identification of hereditary cancer syndromes in newly diagnosed patients with colorectal cancer.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 May 2025

Sears Emma, Dahlquist Jacky, Stayman Sarah, Ko Cynthia, Konnick Eric Q, Cole Allison, Zhang Ying, Kohn Marlana, Henderson Vida, Knerr Sarah

Abstract excerpt

PURPOSE: Germline genetic testing to identify hereditary cancer syndromes in patients newly diagnosed with colorectal cancer (CRC) carries substantial benefits. We examined the feasibility of using patient navigation, an evidence-based approach to reduce structural barriers to recommended care, to improve test completion by increasing pretest counseling attendance. METHODS: We conducted key informant interviews...

Read the complete abstract on PubMed

Topics

Humans
Colorectal Neoplasms
Patient Navigation
Genetic Testing
Neoplastic Syndromes, Hereditary

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Feasibility Studies

Genetic Counseling

Genetic Predisposition to Disease

Source

Identifiers

PMID: 39927451
DOI: 10.1016/j.gim.2025.101372

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

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