Literature DB >> 34782326

Germline Cancer Susceptibility Gene Testing in Unselected Patients with Hepatobiliary Cancers: A Multi-Center Prospective Study.

Pedro Ls Uson Junior1, Katie L Kunze2, Michael A Golafshar2, Douglas Riegert-Johnson3,4,5, Lisa Boardman6, Mitesh J Borad1, Daniel Ahn1, Mohamad B Sonbol1, Douglas O Faigel7, Norio Fukami7, Rahul Pannala7, Kathleen Barrus4, Luke Mountjoy1, Edward D Esplin8, Robert L Nussbaum8, A Keith Stewart1,4,5, Tanios Bekaii-Saab1, N Jewel Samadder9,5,7.   

Abstract

Data from germline testing in unselected patients with hepatobiliary cancers are limited. Identification of germline predisposition can have important implications on cancer treatment and family counseling. To determine prevalence of pathogenic germline variants (PGV) in patients with hepatobiliary cancer, we undertook a prospective multi-site study of germline sequencing using a >80-gene next-generation sequencing platform among patients with hepatobiliary cancers receiving care at Mayo Clinic Cancer Centers between April 1, 2018 and March 31, 2020. Patients were not selected on the basis of stage, family cancer history, ethnicity, or age. Family cascade testing was offered at no cost. Of 205 patients, the median age was 65 years, 58.5% were male, 81% were White, and 64.4% had cholangiocarcinoma, 21.5% hepatocellular carcinoma, 7.8% gallbladder cancer, and 4.3% carcinoma of ampulla of Vater. PGV were found in 15.6% (n = 32) of patients, including 23 (71%) in moderate and high penetrance cancer susceptibility genes. A total of 75% of patients with a positive result would not have been detected using guidelines for genetic evaluation. Prevalence of PGV was 15.7% in intrahepatic cholangiocarcinoma, 17% in extrahepatic cholangiocarcinoma, 15.9% in hepatocellular cancer, and 33% in carcinoma of ampulla of Vater. On the basis of these genetic findings, 55% were potentially eligible for approved precision therapy and/or clinical treatment trials. Universal multi-gene panel testing in hepatobiliary cancers was associated with detection of heritable mutations in over 15% of patients most of whom would not have been tested using current guidelines. Germline testing should be considered in all patients with hepatobiliary cancers. PREVENTION RELEVANCE: Universal multi-gene testing in hepatobiliary cancers was associated with heritable mutations in over 15% of patients, most of whom would not have been tested using current guidelines. 55% were potentially eligible for approved precision therapy and/or clinical treatment trials. Germline testing should be considered in all patients with hepatobiliary cancers. ©2021 The Authors; Published by the American Association for Cancer Research.

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Year:  2021        PMID: 34782326     DOI: 10.1158/1940-6207.CAPR-21-0189

Source DB:  PubMed          Journal:  Cancer Prev Res (Phila)        ISSN: 1940-6215


  1 in total

1.  Effect of comprehensive cancer genomic profiling on therapeutic strategies and clinical outcomes in patients with advanced biliary tract cancer: A prospective multicenter study.

Authors:  Kohichi Takada; Tomohiro Kubo; Junko Kikuchi; Makoto Yoshida; Ayako Murota; Yohei Arihara; Hajime Nakamura; Hiroyuki Nagashima; Hiroki Tanabe; Shintaro Sugita; Yumi Tanaka; Ayana Miura; Yoshihito Ohhara; Atsushi Ishiguro; Hiroshi Yokouchi; Yasuyuki Kawamoto; Yusuke Mizukami; Hirofumi Ohnishi; Ichiro Kinoshita; Akihiro Sakurai
Journal:  Front Oncol       Date:  2022-09-02       Impact factor: 5.738

  1 in total

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