TY - JOUR
T1 - Germline Cancer Susceptibility Gene Testing in Unselected Patients with Hepatobiliary Cancers
T2 - A Multi-Center Prospective Study
AU - Uson, Pedro L.S.
AU - Kunze, Katie L.
AU - Golafshar, Michael A.
AU - Riegert-Johnson, Douglas
AU - Boardman, Lisa
AU - Borad, Mitesh J.
AU - Ahn, Daniel
AU - Sonbol, Mohamad B.
AU - Faigel, Douglas O.
AU - Fukami, Norio
AU - Pannala, Rahul
AU - Barrus, Kathleen
AU - Mountjoy, Luke
AU - Esplin, Edward D.
AU - Nussbaum, Robert L.
AU - Stewart, A. Keith
AU - Bekaii-Saab, Tanios
AU - Samadder, N. Jewel
N1 - Funding Information:
The study was funded by Mayo Transform the Practice Grant, Mayo Clinic Center for Individualized Medicine, Desert Mountain Members' CARE Foundation, David and Twila Woods Foundation. The funding sources did not play a role in the design, conduct or reporting of the study or in the decision to submit the article for publication. Support for this project was provided by Mayo Transform the Practice Grant, Mayo Clinic Center for Individualized Medicine, Desert Mountain Members' CARE Foundation, David and Twila Woods Foundation and a Faculty Career Development Award from the Gerstner Foundation (N. Jewel Samadder). We would like to thank the following persons for their assistance with this project-Sydney Welp, Jessie Fox, Plush Gutierrez, Sara Hernandez, Sharon Levy, Eric Nelson, Rachel Colburn, Anne Bofferding, Arta Palaj, Lorelei Bandel, Megan Mulcahy, and David Upjohn.
Funding Information:
Support for this project was provided by Mayo Transform the Practice Grant, Mayo Clinic Center for Individualized Medicine, Desert Mountain Members’ CARE Foundation, David and Twila Woods Foundation and a Faculty Career Development Award from the Gerstner Foundation (N. Jewel Samadder).
Funding Information:
The study was funded by Mayo Transform the Practice Grant, Mayo Clinic Center for Individualized Medicine, Desert Mountain Members’ CARE Foundation, David and Twila Woods Foundation. The funding sources did not play a role in the design, conduct or reporting of the study or in the decision to submit the article for publication.
Publisher Copyright:
© 2021 The Authors; Published by the American Association for Cancer Research
PY - 2022/2
Y1 - 2022/2
N2 - 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 ¼ 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.
AB - 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 ¼ 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.
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U2 - 10.1158/1940-6207.CAPR-21-0189
DO - 10.1158/1940-6207.CAPR-21-0189
M3 - Article
C2 - 34782326
AN - SCOPUS:85124434489
SN - 1940-6207
VL - 15
SP - 121
EP - 128
JO - Cancer Prevention Research
JF - Cancer Prevention Research
IS - 2
ER -