Universal Genetic Testing vs. Guideline-Directed Testing for Hereditary Cancer Syndromes Among Traditionally Underrepresented Patients in a Community Oncology Program

Background Detection of pathogenic germline variants (PGVs) has implications for cancer screening, prognosis, treatment selection, clinical trial enrollment, and family testing. Published guidelines provide indications for PGV testing, determined by clinical and demographic factors, but their applic...

Descripción completa

Detalles Bibliográficos
Autores principales: Jones, Jeremy C, Golafshar, Michael A, Coston, Tucker W, Rao, Rohit, Wysokinska, Ewa, Johnson, Elizabeth, Esplin, Edward D, Nussbaum, Robert L, Heald, Brandie, Klint, Margaret, Barrus, Kathleen, Uson Jr., Pedro L, Nguyen, Cuong C, Colon-Otero, Gerald, Bekaii-Saab, Tanios S, Dronca, Roxana, Kunze, Katie L, Samadder, N. Jewel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173369/
https://www.ncbi.nlm.nih.gov/pubmed/37181954
http://dx.doi.org/10.7759/cureus.37428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173369/
https://www.ncbi.nlm.nih.gov/pubmed/37181954
http://dx.doi.org/10.7759/cureus.37428

Ejemplares similares