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ID 65974
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Author
Horiguchi, Shigeru Department of Gastroenterology and Hepatology, Okayama University Hospital
Matsumoto, Kazuyuki Department of Gastroenterology and Hepatology, Okayama University Hospital ORCID Kaken ID publons
Morimoto, Kosaku Department of Gastroenterology and Hepatology, Okayama University Hospital
Matsumi, Akihiro Department of Gastroenterology and Hepatology, Okayama University Hospital
Terasawa, Hiroyuki Department of Gastroenterology and Hepatology, Okayama University Hospital
Fujii, Yuki Department of Gastroenterology and Hepatology, Okayama University Hospital
Yamazaki, Tatsuhiro Department of Gastroenterology and Hepatology, Okayama University Hospital
Tsutsumi, Koichiro Department of Gastroenterology and Hepatology, Okayama University Hospital ORCID Kaken ID researchmap
Kato, Hironari Department of Gastroenterology and Hepatology, Okayama University Hospital ORCID Kaken ID researchmap
Abstract
We investigated the effect of modified FOLFIRINOX (mFFX) in unresectable pancreatic cancer by retrospectively analyzing the cases of 43 patients who underwent BRCA testing (germline, n=11; somatic, n=26; both germline and somatic, n=6). The association between BRCA mutations and therapeutic effect was clarified. Six patients tested positive for germline pathogenic variants. Familial pancreatic cancer (33% vs. 3%, p=0.006) and peritoneal disseminated lesions (66% vs. 8%, p<0.001) were significantly more common in patients with germline pathogenic variants. The partial response (PR) rate was 100% in the germline BRCA-positive patients, and 27% in the germline BRCA-negative patients (p<0.001). The median progression-free survival (PFS) was not reached for any germline BRCA-positive patients but was 9.0 months for the germline BRCA-negative patients (p=0.042). Patients with stage IV BRCA-associated pancreatic cancer had better overall survival than those with non-BRCA-associated pancreatic cancer, although the difference was nonsignificant (not reached vs. 655 days, p=0.061). Our results demonstrate that a PR and prolonged PFS can be expected in germline BRCA-positive patients after treatment with mFFX. Our findings also suggest that germline BRCA pathogenic variants may be useful as biomarkers for the therapeutic effect of mFFX in patients with pancreatic cancer.
Keywords
BRCA
FOLFIRINOX
pancreatic cancer
progression-free survival
pathogenic variant
Amo Type
Original Article
Publication Title
Acta Medica Okayama
Published Date
2023-10
Volume
volume77
Issue
issue5
Publisher
Okayama University Medical School
Start Page
517
End Page
525
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
Copyright Ⓒ 2023 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT