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

Filipa Lynce, Mark Robson
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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.

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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。
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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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