Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study

To report the prevalence and outcomes of unselected pancreatic cancer (PC) patients with pathogenic/likely pathogenic germline variants (PGVs) detected using a universal testing approach. METHODS: We undertook a prospective, multisite study of germline sequencing using a >80 gene next-generation...

Descripción completa

Detalles Bibliográficos
Autores principales: Uson, Pedro L. S., Samadder, N. Jewel, Riegert-Johnson, Douglas, Boardman, Lisa, Borad, Mitesh J., Ahn, Daniel, Sonbol, Mohamad B., Faigel, Douglas O., Fukami, Norio, Pannala, Rahul, Kunze, Katie, Golafshar, Michael, Klint, Margaret, Esplin, Edward D., Nussbaum, Robert L., Stewart, A. Keith, Bekaii-Saab, Tanios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500569/
https://www.ncbi.nlm.nih.gov/pubmed/34620795
http://dx.doi.org/10.14309/ctg.0000000000000414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500569/
https://www.ncbi.nlm.nih.gov/pubmed/34620795
http://dx.doi.org/10.14309/ctg.0000000000000414

Ejemplares similares