Clinical Use of PARP Inhibitors in BRCA Mutant and Non-BRCA Mutant Breast Cancer.

Q2 Medicine
Filipa Lynce, Mark Robson
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引用次数: 0

Abstract

The use of poly(ADP-ribose) polymerase (PARP) inhibitors for the treatment of patients with germline BRCA mutations (gBRCAm) and breast cancer, both in the early and advanced settings, is a success of genomically-directed treatment. These agents have been shown to be associated with longer progression-free survival when compared to standard chemotherapy, with an acceptable toxicity profile. A recent randomized trial demonstrated improved survival with the use of olaparib for 2 years compared to placebo in patients with early-stage high risk gBRCAm associated breast cancer. Ongoing research efforts are focused on identifying patients beyond those with BRCA1/2 or PALB2 mutations who may benefit from PARP inhibitors, exploring the overlapping mechanisms of resistance between platinum and PARP inhibitors and developing agents with less toxicity that will allow combinational strategies.

PARP抑制剂在BRCA突变型和非BRCA突变型乳腺癌中的临床应用
使用聚(adp -核糖)聚合酶(PARP)抑制剂治疗生殖系BRCA突变(gBRCAm)和乳腺癌患者,无论是在早期还是晚期,都是基因组定向治疗的成功。与标准化疗相比,这些药物已被证明具有更长的无进展生存期,并且具有可接受的毒性。最近的一项随机试验表明,与安慰剂相比,使用奥拉帕尼可改善早期高危gBRCAm相关乳腺癌患者2年的生存率。正在进行的研究工作主要集中在鉴定可能受益于PARP抑制剂的BRCA1/2或PALB2突变以外的患者,探索铂和PARP抑制剂之间的重叠耐药机制,以及开发毒性较小的药物,从而实现联合策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer treatment and research
Cancer treatment and research Medicine-Oncology
CiteScore
1.00
自引率
0.00%
发文量
11
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