Assessment of a cancer genomic profile test for patients with metastatic breast cancer

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作者
Ippei Fukada
Seiichi Mori
Naomi Hayashi
Mari Hosonaga
Masumi Yamazaki
Xiaofei Wang
Saori Kawai
Lina Inagaki
Yukinori Ozaki
Kokoro Kobayashi
Fumikata Hara
Takayuki Kobayashi
Arisa Ueki
Tomo Osako
Akiko Tonooka
Kengo Takeuchi
Takayuki Ueno
Toshimi Takano
Shinji Ohno
Shunji Takahashi
机构
[1] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,Genomic Medicine
[2] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,Breast Medical Oncology
[3] Japanese Foundation for Cancer Research,Division of Cancer Genomics
[4] Cancer Institute,Medical Oncology
[5] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,The Center for Advanced Medical Development
[6] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,Clinical Genetic Oncology
[7] Cancer Institute Hospital,Division of Pathology, Cancer Institute
[8] Japanese Foundation for Cancer Research,Department of Pathology, Cancer Institute Hospital
[9] Japanese Foundation for Cancer Research,Pathology Project for Molecular Targets, Cancer Institute
[10] Japanese Foundation for Cancer Research,Breast Surgery
[11] Japanese Foundation for Cancer Research,Breast Oncology Center
[12] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,undefined
[13] The Cancer Institute Hospital of Japanese Foundation for Cancer Research,undefined
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摘要
Comprehensive cancer genomic profile (CGP) tests are being implemented under Japanese universal health insurance system. However, the clinical usefulness of CGP test for breast cancer patients has not been evaluated. Of the 310 patients who underwent CGP testing at our institution between November 2019 and April 2021, 35 patients with metastatic breast cancer whose treatment strategy was discussed by our molecular tumor board within the study period were investigated after exclusion of 2 cases that could not be analyzed. The turn-around time, drug accessibility, and germline identification detection were evaluated. The subtype was luminal in 20 patients (57.1%), triple-negative in 12 patients (34.3%), and luminal-HER2 in 3 patients (8.6%). Actionable gene mutations were detected in 30 patients (85.7%), and 7 patients (20.0%) were recommended for clinical trial participation, with the drug administered to 2 patients (5.7%). Three patients (8.6%) died due to disease progression before the test results were disclosed. We report the results of an initial assessment of the utility of CGP testing for patients with metastatic breast cancer under Japanese universal health insurance system. Conducting CGP tests at a more appropriate time could provide patients with greater benefit from treatments based on their specific gene mutations.
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