論文種別 原著(症例報告除く)
言語種別 英語
査読の有無 その他(不明)
表題 Clinical utility and characteristics of comprehensive genomic profiling tests in patients with gynecologic cancer: a multi-institutional survey in Kinki District, Japan.
掲載誌名 正式名:International journal of clinical oncology
略  称:Int J Clin Oncol
ISSNコード:14377772/13419625
掲載区分国外
巻・号・頁 30(10),pp.2128-2137
著者・共著者 Shinichi Terada, Tomohito Tanaka, Yoji Hisamatsu, Masato Kita, Mana Taki, Koji Yamanoi, Hiroyuki Fujita, Seiko Kato, Hisashi Kataoka, Taisuke Mori, Hidekatsu Nakai, Noriomi Matsumura, Hiroki Nishimura, Tsukuru Amano, Naohisa Masuko, Yoshito Terai, Madoka Suruga, Makoto Murakami, Mariya Kobayashi, Satoshi Nakagawa, Hisanori Matsumoto, Yusuke Fujikami, Michihide Maeda, Shoji Kamiura, Kyohei Nishikawa, Yosuke Fukui, Tomoko Ueda, Hiroshi Tsubamoto, Sayaka Ueno, Takashi Shibutani, Ayame Teramoto, Yasushi Mabuchi, Kazuhiko Ino, Takahito Motoyama, Takuya Aoki, Ryo Nakazawa, Fuminori Ito, Nao Terayama, Masanori Kanemura, Azusa Sakurai, Yumi Takao, Masahide Ohmichi
発行年月 2025/10
概要 BACKGROUND:Comprehensive genomic profiling (CGP) has been used to identify mutations in several hundred cancer-related genes. Patients may receive treatment that targets specific genetic mutations revealed by CGP. This study aimed to investigate the usefulness of CGP in gynecologic malignancies.METHODS:Hospital records including CGP and clinical information were reviewed from 20 institutions in the Kinki District of Japan for patients with gynecological malignancies who underwent CGP.RESULTS:A total of 724 patients were included, of whom 162 had cervical cancer, 157 had endometrial cancer, 327 had ovarian cancer, 29 had other cancers, and 49 had sarcomas. Actionable gene alterations were identified in 370 (51.1%). The most commonly altered genes were PIK3CA (14.4%), high loss of heterozygosity (12.4%), and high tumor mutation burden (10.9%). Matched therapy, based on actionable gene alterations, was administered to 73 patients (10.1%). Of these, 23 patients received matched therapy for a high tumor mutation burden, 10 for high microsatellite instability and BRCA1/2, six for ERBB2, and five for PIK3CA. Twenty-five patients died before receiving their CGP results. The objective response and disease control rates were 23.6% and 41.8%, respectively. Of the 122 patients to whom genetic counseling was recommended, 68 accepted.CONCLUSIONS:CGP testing for gynecological malignancies in Japan may improve therapeutic efficacy. However, several issues remain to be addressed, including the low matched therapy rate and death prior to availability of CGP test results.
DOI 10.1007/s10147-025-02835-w
PMID 40694280