| Literature DB >> 30792639 |
Albert Grinshpun1, Yonaton Zarbiv1, Jason Roszik2, Vivek Subbiah3, Ayala Hubert1.
Abstract
Pancreatic adenocarcinoma (PDAC) has a grim prognosis. Molecular and genomic analyses revealed that the striking majority of these tumors are driven by KRAS mutation, currently not amenable to targeted therapy. However, other driver mutations were found in a small fraction of patients. Herein we report of 3 cases of patients with metastatic PDAC and wildtype KRAS, found to harbor BRAF or RET pathogenic alterations. The patients were treated with targeted therapies with variable success. In our opinion, those proof-of-concept cases argue in favor of additional research and clinical trials' effort in this small but significant PDAC population with uncommon driver mutations.Entities:
Keywords: BRAF; KRAS; Pancreatic adenocarcinoma; RET; Targeted therapy
Year: 2019 PMID: 30792639 PMCID: PMC6381925 DOI: 10.1159/000496018
Source DB: PubMed Journal: Case Rep Oncol ISSN: 1662-6575