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PARP inhibitors alone and in combination with other biological agents in homologous recombination deficient epithelial ovarian cancer: From the basic research to the clinic

机译:单独的PARP抑制剂并与其他生物剂组合在同源重组缺乏上皮卵巢癌中:从基本研究到诊所

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Hereditary epithelial ovarian cancer [EOC] in germline BRCA mutation (gBRCAm) carriers has a distinct clinical behavior characterized by younger age, high- grade serous histology, advanced stage, visceral distribution of disease, high response to platinum and other non-platinum agents and better clinical outcome. Sporadic EOC with homologous recombination deficiency [HDR] but no gBRCAm has the same biological and clinical behavior as EOC in gBRCAm carriers ("BRCAness"phenotype). Biomarkers are in development to enable an accurate definition of molecular features of BRCAness phenotype, and trials are warranted to determine whether such HDR signature will predict sensitivity to PARP inhibitors in sporadic EOC. Moreover, the link between PARP inhibition and angiogenesis suppression, the immunologic properties of EOC in gBRCAm carriers, the HRD induced by PI3K( inhibition in EOC cells in vitro strongly support novel clinical trials testing the combination of PARP inhibitors with other biological agents. (C) 2017 Elsevier B.V. All rights reserved.
机译:种系卵巢癌症癌症(Gbrcam)突变(GbrCam)载体具有明显的临床行为,其特征是较年轻的年龄,高级浆液组织学,晚期疾病,疾病的高度反应,对铂和其他非铂族的高度反应更好的临床结果。具有同源重组缺陷的零星EOC [HDR]但没有GBRCAM在GBRCAM载体中具有与EOC相同的生物和临床行为(“BRCANESS”表型)。生物标志物在开发中,能够准确定义Brcaness表型的分子特征,并保证试验以确定这些HDR签名是否将预测零星EOC中对PARP抑制剂的敏感性。此外,PARP抑制和血管生成抑制之间的链接,GBRCAM载体中EOC的免疫特性,PI3K诱导的HRD(在体外抑制EC细胞强烈支持新的临床试验,测试PARP抑制剂与其他生物剂的组合。(C )2017年Elsevier BV保留所有权利。

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