Clinical characterization of patients with gBRCA1/2 mutation-positive unresectable pancreatic cancer: a multicenter prospective study

Author:

Kubo Tomohiro1,Muramatsu Joji1,Arihara Yohei1,Murota Ayako23,Ishikawa Kazuma1,Yoshida Makoto1,Nagashima Hiroyuki4,Tamura Fumito4,Ikeda Yuki5,Usami Makoto6,Ono Michihiro7,Nakamura Hajime18,Watanabe Daichi9,Shibata Takanori10,Kasahara Kaoru11,Sakurai Akihiro2,Takada Kohichi1

Affiliation:

1. Department of Medical Oncology, Sapporo Medical University School of Medicine , Sapporo , Japan

2. Department of Medical Genetics and Genomics, Sapporo Medical University School of Medicine , Sapporo , Japan

3. Department of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine , Sapporo , Japan

4. Department of Gastroenterology, Hokkaido Cancer Center , Sapporo , Japan

5. Department of Gastroenterology, Oji General Hospital , Tomakomai , Japan

6. Department of Medical Oncology, Steel Memorial Muroran Hospital , Muroran , Japan

7. Department of Gastroenterology, Steel Memorial Muroran Hospital , Muroran , Japan

8. Department of Gastroenterology, Otaru Ekisaikai Hospital , Otaru , Japan

9. Department of Gastroenterology, Japanese Red Cross Date Hospital , Date , Japan

10. Department of Gastroenterology, Rumoi City Hospital , Rumoi , Japan

11. Department of Gastroenterology, Hakodate Goryoukaku Hospital , Hakodate , Japan

Abstract

Abstract Background Accumulating evidence has demonstrated platinum-based chemotherapy followed by maintenance therapy with a poly Adenosine diphosphate (ADP)-ribose polymerase inhibitor (olaparib) show benefits in unresectable pancreatic cancer with a germline (g)BRCA1/2 mutation. Evaluation of the germline BRCA1 and BRCA2 mutation is essential for making decisions on a treatment strategy for patients with unresectable pancreatic cancer. However, the detection rates of germline BRCA1 and BRCA2 mutations and efficacy of maintenance with olaparib remain undetermined, prospectively, in Japan. Methods & Results In this prospective analysis, the rate of germline BRCA1 and BRCA2 mutations and efficacy of chemotherapy were analyzed in 136 patients with pancreatic cancer who underwent BRACAnalysis® (85 patients) or FoundationOne® CDx (51 patients) between January 2020 and July 2022. A total of six patients (4.4%) had a germline BRCA1 and BRCA2 mutation. Five patients were treated with modified FOLFIRINOX and one with fluorouracil and oxaliplatin. All patients continued platinum-based chemotherapy for ˃4 months and were subsequently treated with olaparib as a maintenance therapy. The response rate to platinum-based chemotherapy in the germline BRCA1 and BRCA2 mutation-positive group was significantly better than that of the germline BRCA1 and BRCA2 mutation-negative group (66% vs 23%, P = 0.04). All patients harbouring a germline BRCA1 and BRCA2 mutation were able to switch to olaparib. The median progression-free survival using olaparib was 5.7 months (range 3.0–9.2). Conclusions The rate of germline BRCA1 and BRCA2 mutations found in patients with unresectable pancreatic cancer was comparable to those of previous studies. An analysis of germline BRCA1 and BRCA2 mutations has benefits for all patients with unresectable pancreatic cancer with regard to decisions on therapeutic strategies in a clinical practice setting.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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