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Olaparib Monotherapy for -Mutated High-Grade Serous Endometrial Cancer.

作者信息

Nakamura Kohei, Aimono Eriko, Tanishima Shigeki, Imai Mitsuho, Nagatsuma Akiko Kawano, Hayashi Hideyuki, Yoshimura Yuki, Nakayama Kentaro, Kyo Satoru, Nishihara Hiroshi

机构信息

Genomics Unit, Keio Cancer Center, Keio University School of Medicine, Tokyo, Japan.

Department of Biomedical Informatics, Kansai Division, Mitsubishi Space Software, Tokyo, Japan.

出版信息

JCO Precis Oncol. 2020 Apr 9;4. doi: 10.1200/PO.19.00368. eCollection 2020.

DOI:10.1200/PO.19.00368
PMID:32923896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7446499/
Abstract
摘要

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Mutations in homologous recombination repair genes in patients with metastatic endometrial cancer: association with clinical characteristics and prognosis.

本文引用的文献

1
Prevalence of Homologous Recombination-Related Gene Mutations Across Multiple Cancer Types.多种癌症类型中同源重组相关基因突变的患病率。
JCO Precis Oncol. 2018;2018. doi: 10.1200/PO.17.00286. Epub 2018 Jul 23.
2
Mutation status of RAD51C, PALB2 and BRIP1 in 100 Japanese familial breast cancer cases without BRCA1 and BRCA2 mutations.100例无BRCA1和BRCA2突变的日本家族性乳腺癌病例中RAD51C、PALB2和BRIP1的突变状态
Cancer Sci. 2017 Nov;108(11):2287-2294. doi: 10.1111/cas.13350. Epub 2017 Sep 18.
3
Homologous Recombination Deficiency: Exploiting the Fundamental Vulnerability of Ovarian Cancer.
转移性子宫内膜癌患者同源重组修复基因的突变:与临床特征及预后的关联
J Gynecol Oncol. 2025 Jul;36(4):e62. doi: 10.3802/jgo.2025.36.e62. Epub 2025 Jan 26.
4
Clinical application of whole-genome sequencing of solid tumors for precision oncology.实体瘤全基因组测序在精准肿瘤学中的临床应用。
Exp Mol Med. 2024 Aug;56(8):1856-1868. doi: 10.1038/s12276-024-01288-x. Epub 2024 Aug 13.
5
Homologous Recombination Deficiency Across Subtypes of Primary Breast Cancer.原发性乳腺癌各亚型的同源重组缺陷。
JCO Precis Oncol. 2023 Sep;7:e2300338. doi: 10.1200/PO.23.00338.
6
Complete Pathologic Response to PARP Inhibitor Olaparib in a Patient with Stage IVB Recurrent Endometrioid Endometrial Adenocarcinoma.一名IVB期复发性子宫内膜样腺癌患者对PARP抑制剂奥拉帕尼的完全病理反应
J Clin Med. 2023 Jun 4;12(11):3839. doi: 10.3390/jcm12113839.
7
Targeting homologous recombination deficiency in uterine leiomyosarcoma.针对子宫平滑肌肉瘤的同源重组缺陷。
J Exp Clin Cancer Res. 2023 May 4;42(1):112. doi: 10.1186/s13046-023-02687-0.
8
Spectrum of BRCA1 interacting helicase 1 aberrations and potential prognostic and therapeutic implication: a pan cancer analysis.BRCA1 相互作用解旋酶 1 异常的谱及其潜在的预后和治疗意义:泛癌分析。
Sci Rep. 2023 Mar 17;13(1):4435. doi: 10.1038/s41598-023-31109-6.
9
Estimating copy number to determine BRCA2 deletion status and to expect prognosis in localized prostate cancer.评估拷贝数以确定 BRCA2 缺失状态并预测局限性前列腺癌的预后。
Cancer Med. 2023 Apr;12(7):8154-8165. doi: 10.1002/cam4.5617. Epub 2023 Jan 16.
10
Therapeutic implications of germline vulnerabilities in DNA repair for precision oncology.胚系 DNA 修复缺陷与精准肿瘤学的治疗相关性
Cancer Treat Rev. 2022 Mar;104:102337. doi: 10.1016/j.ctrv.2021.102337. Epub 2022 Jan 5.
同源重组缺陷:利用卵巢癌的根本脆弱性
Cancer Discov. 2015 Nov;5(11):1137-54. doi: 10.1158/2159-8290.CD-15-0714. Epub 2015 Oct 13.
4
Endometrial cancer.子宫内膜癌。
Lancet. 2016 Mar 12;387(10023):1094-1108. doi: 10.1016/S0140-6736(15)00130-0. Epub 2015 Sep 6.
5
Review of poly (ADP-ribose) polymerase (PARP) mechanisms of action and rationale for targeting in cancer and other diseases.聚(ADP - 核糖)聚合酶(PARP)作用机制综述以及在癌症和其他疾病中作为靶向治疗的理论依据。
Crit Rev Eukaryot Gene Expr. 2014;24(1):15-28. doi: 10.1615/critreveukaryotgeneexpr.2013006875.
6
Integrated genomic characterization of endometrial carcinoma.子宫内膜癌的综合基因组特征分析。
Nature. 2013 May 2;497(7447):67-73. doi: 10.1038/nature12113.
7
Patterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancer.基因组杂合性丢失模式预测上皮性卵巢癌同源重组修复缺陷。
Br J Cancer. 2012 Nov 6;107(10):1776-82. doi: 10.1038/bjc.2012.451. Epub 2012 Oct 9.
8
Ploidy and large-scale genomic instability consistently identify basal-like breast carcinomas with BRCA1/2 inactivation.倍性和大规模基因组不稳定性一致鉴定出具有 BRCA1/2 失活的基底样乳腺癌。
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Molecular targets and targeted therapeutics in endometrial cancer.子宫内膜癌的分子靶点和靶向治疗。
Curr Opin Oncol. 2012 Sep;24(5):554-63. doi: 10.1097/CCO.0b013e328354e585.
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Telomeric allelic imbalance indicates defective DNA repair and sensitivity to DNA-damaging agents.端粒等位基因不平衡表明DNA修复缺陷以及对DNA损伤剂敏感。
Cancer Discov. 2012 Apr;2(4):366-375. doi: 10.1158/2159-8290.CD-11-0206. Epub 2012 Mar 22.