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  1. 原著論文

Mutation profiling of uterine cervical cancer patients treated with definitive radiotherapy

https://repo.qst.go.jp/records/81479
https://repo.qst.go.jp/records/81479
a41a4fc8-e81b-4f81-b2be-1b62a49f02fd
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-12-28
タイトル
タイトル Mutation profiling of uterine cervical cancer patients treated with definitive radiotherapy
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Yoshimoto, Yuya

× Yoshimoto, Yuya

WEKO 1013641

Yoshimoto, Yuya

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Sasaki, Yasushi

× Sasaki, Yasushi

WEKO 1013642

Sasaki, Yasushi

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Murata, Kazutoshi

× Murata, Kazutoshi

WEKO 1013643

Murata, Kazutoshi

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Shin-ei, Noda

× Shin-ei, Noda

WEKO 1013644

Shin-ei, Noda

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Miyasaka, Yuhei

× Miyasaka, Yuhei

WEKO 1013645

Miyasaka, Yuhei

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Hamamoto, Junko

× Hamamoto, Junko

WEKO 1013646

Hamamoto, Junko

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Furuya, Mio

× Furuya, Mio

WEKO 1013647

Furuya, Mio

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Hirato, Junko

× Hirato, Junko

WEKO 1013648

Hirato, Junko

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Suzuki, Yoshiyuki

× Suzuki, Yoshiyuki

WEKO 1013649

Suzuki, Yoshiyuki

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Ohno, Tatsuya

× Ohno, Tatsuya

WEKO 1013650

Ohno, Tatsuya

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Tokino, Takashi

× Tokino, Takashi

WEKO 1013651

Tokino, Takashi

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Oike, Takahiro

× Oike, Takahiro

WEKO 1013652

Oike, Takahiro

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Nakano, Takashi

× Nakano, Takashi

WEKO 1013653

Nakano, Takashi

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Tatsuya, Ohno

× Tatsuya, Ohno

WEKO 1013654

en Tatsuya, Ohno

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Takashi, Nakano

× Takashi, Nakano

WEKO 1013655

en Takashi, Nakano

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抄録
内容記述タイプ Abstract
内容記述 Objective
To elucidate tumor mutation profiles associated with outcomes of uterine cervical cancer (UCC) patients treated with definitive radiotherapy.

Methods
Ninety-eight patients with newly diagnosed and pathologically confirmed UCC (82 squamous cell carcinomas, 12 adenocarcinomas, and four adenosquamous carcinomas) who were treated with definitive radiotherapy were analyzed. DNA was extracted from pre-treatment tumor biopsy specimens. The exons of 409 cancer-related genes were sequenced using a next-generation sequencer. Genetic mutations were identified and analyzed for correlations with clinical outcome.

Results
Recurrent mutations were observed in PIK3CA (35.7%), ARID1A (25.5%), NOTCH1 (19.4%), FGFR3 (16.3%), FBXW7 (19.4%), TP53 (13.3%), EP300 (12.2%), and FGFR4 (10.2%). The prevalence of mutations in FGFR family genes (i.e., FGFR1–4) was almost as high (24.5%) as that in PIK3CA and ARID1A, both of which are well-studied drivers of UCC. Fifty-five percent (21 of 38) of the identified FGFR mutations were located in the FGFR protein tyrosine kinase domain. Five-year progression-free survival (PFS) rates for FGFR mutation-positive patients (n = 24) were significantly worse than those for FGFR mutation-negative patients (n = 74) (43.9% vs. 68.5%, respectively; P = 0.010). Multivariate analysis identified FGFR mutations as significant predictors of worse 5 year PFS (P = 0.005), independent of clinicopathological variables.

Conclusions
FGFR mutations are associated with worse PFS in UCC patients treated with definitive radiotherapy. These results warrant further validation in prospective studies.
書誌情報 Gynecologic Oncology

巻 159, 号 2, p. 546-553, 発行日 2020-12
出版者
出版者 Elsevier
ISSN
収録物識別子タイプ ISSN
収録物識別子 0090-8258
DOI
識別子タイプ DOI
関連識別子 10.1016/j.ygyno.2020.08.020
関連サイト
識別子タイプ URI
関連識別子 https://www.sciencedirect.com/science/article/pii/S009082582033821X?via%3Dihub
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