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决策:何时、针对谁使用哪种 PARP 抑制剂。

The DecisionWhich PARP Inhibitor to Use for Whom and When.

机构信息

National Cancer Institute, Bethesda, Maryland.

出版信息

Clin Cancer Res. 2017 Dec 1;23(23):7155-7157. doi: 10.1158/1078-0432.CCR-17-2186. Epub 2017 Oct 3.

DOI:10.1158/1078-0432.CCR-17-2186
PMID:28974545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5712252/
Abstract

Rucaparib, a polyADPribose polymerase inhibitor (PARPi), was approved recently for use in women with high-grade serous ovarian cancer (HGSOC). It is now one of three approved PARPi for use in recurrent ovarian cancer, a family of agents that has changed the HGSOC treatment landscape and outcome. .

摘要

鲁卡帕利,一种聚 ADP 核糖聚合酶抑制剂(PARPi),最近被批准用于治疗高级别浆液性卵巢癌(HGSOC)。它现在是三种已批准用于复发性卵巢癌的 PARPi 之一,这一类药物改变了 HGSOC 的治疗格局和结果。

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本文引用的文献

1
Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial.奥拉帕利片作为 BRCA1/2 突变的铂敏感复发性卵巢癌患者的维持治疗(SOLO2/ENGOT-Ov21):一项双盲、随机、安慰剂对照、III 期临床试验。
Lancet Oncol. 2017 Sep;18(9):1274-1284. doi: 10.1016/S1470-2045(17)30469-2. Epub 2017 Jul 25.
2
FDA Approval Summary: Rucaparib for the Treatment of Patients with Deleterious Mutation-Associated Advanced Ovarian Cancer.美国食品药品监督管理局批准概要:芦卡帕利治疗携带有害突变相关的晚期卵巢癌患者。
Clin Cancer Res. 2017 Dec 1;23(23):7165-7170. doi: 10.1158/1078-0432.CCR-17-1337. Epub 2017 Jul 27.
3
The 'Pushmi-Pullyu' of DNA REPAIR: Clinical Synthetic Lethality.DNA修复中的“双头怪”:临床合成致死性
Trends Cancer. 2016 Nov;2(11):646-656. doi: 10.1016/j.trecan.2016.10.014. Epub 2016 Nov 23.
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PARP inhibitors: Synthetic lethality in the clinic.聚(ADP-核糖)聚合酶抑制剂:临床中的合成致死性
Science. 2017 Mar 17;355(6330):1152-1158. doi: 10.1126/science.aam7344. Epub 2017 Mar 16.
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Rucaparib in relapsed, platinum-sensitive high-grade ovarian carcinoma (ARIEL2 Part 1): an international, multicentre, open-label, phase 2 trial.鲁卡帕利治疗复发铂类敏感型高级别卵巢癌(ARIEL2 研究第 1 部分):一项国际多中心、开放标签、2 期临床试验。
Lancet Oncol. 2017 Jan;18(1):75-87. doi: 10.1016/S1470-2045(16)30559-9. Epub 2016 Nov 29.
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Targeting the DNA Damage Response in Cancer.靶向癌症的 DNA 损伤反应。
Mol Cell. 2015 Nov 19;60(4):547-60. doi: 10.1016/j.molcel.2015.10.040.
7
Combination cediranib and olaparib versus olaparib alone for women with recurrent platinum-sensitive ovarian cancer: a randomised phase 2 study.联合 Cediranib 和奥拉帕利对比奥拉帕利单药治疗铂类敏感复发性卵巢癌患者的随机 2 期研究。
Lancet Oncol. 2014 Oct;15(11):1207-14. doi: 10.1016/S1470-2045(14)70391-2. Epub 2014 Sep 10.
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Ovarian cancer.卵巢癌。
Lancet. 2014 Oct 11;384(9951):1376-88. doi: 10.1016/S0140-6736(13)62146-7. Epub 2014 Apr 21.
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Efficacy of chemotherapy in BRCA1/2 mutation carrier ovarian cancer in the setting of PARP inhibitor resistance: a multi-institutional study.BRCA1/2 突变携带者卵巢癌中 PARP 抑制剂耐药后的化疗疗效:一项多机构研究。
Clin Cancer Res. 2013 Oct 1;19(19):5485-93. doi: 10.1158/1078-0432.CCR-13-1262. Epub 2013 Aug 6.
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Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors.临床 PARP 抑制剂对 PARP1 和 PARP2 的捕获。
Cancer Res. 2012 Nov 1;72(21):5588-99. doi: 10.1158/0008-5472.CAN-12-2753.