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Rucaparib in ovarian cancer: an update on safety efficacy and place in therapy

机译:rucaparib在卵巢癌中的应用:安全性功效和治疗方法的最新进展

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摘要

Rucaparib is a poly (ADP-ribose) polymerase (PARP) inhibitor and potent inhibitor of PARP1, PARP2 and PARP3 enzymes. Phase II and III trials have documented that rucaparib has single-agent antitumor activity in patients with high-grade ovarian carcinoma, with both BRCA-mutated (germline and somatic) and with homologous recombination deficiency (HRD). Rucaparib as a maintenance treatment showed increased progression-free survival in patients with ovarian carcinoma who achieved a response to platinum-based chemotherapy, with an acceptable safety profile. The approval of this drug, along with the companion diagnostic FoundationFocus CDxBRCA test represents an important new therapeutic option in the treatment of ovarian cancer. This article reviews the mechanisms of action, safety, pharmacokinetics and pharmacodynamics and indications for use of rucaparib as well as future trials.
机译:Rucaparib是一种聚(ADP-核糖)聚合酶(PARP)抑制剂,是PARP1,PARP2和PARP3酶的有效抑制剂。 II和III期试验已证明,rucaparib对BRCA突变型(种系和体细胞型)和同源重组缺陷型(HRD)的晚期卵巢癌患者具有单药抗肿瘤活性。 Rucaparib作为维持治疗方法显示,对铂类化学疗法有反应的卵巢癌患者,其无进展生存期增加,并且具有可接受的安全性。该药物的批准以及伴随的诊断性FoundationFocus CDxBRCA测试代表了卵巢癌治疗中的重要新治疗选择。本文回顾了作用机理,安全性,药代动力学和药效学以及使用rucaparib的适应症以及未来的试验。

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