Suppr超能文献

他拉唑帕利联合恩杂鲁胺治疗转移性去势抵抗性前列腺癌的评估。

An evaluation of talazoparib plus enzalutamide for the treatment of metastatic castration-resistant prostate cancer.

作者信息

Serra Riccardo, Giunta Emilio Francesco, Schepisi Giuseppe, Brighi Nicole, Montanari Daniela, Lolli Cristian, Bleve Sara, Piras Margherita, Palmieri Giuseppe, Scartozzi Mario, Paliogiannis Panagiotis, De Giorgi Ugo

机构信息

Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy.

Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.

出版信息

Expert Rev Anticancer Ther. 2024 Dec;24(12):1221-1227. doi: 10.1080/14737140.2024.2445152. Epub 2024 Dec 25.

Abstract

INTRODUCTION

Prostate cancer (PCa) is the second most common cancer diagnosis among men worldwide, with poor prognosis in its advanced stage. Treatment strategies have evolved, including the use of androgen receptor pathway inhibitors (ARPIs) and poly (ADP-ribose) polymerase inhibitors (PARPis).

AREAS COVERED

This review evaluates the clinical efficacy, safety, and future potential of combining talazoparib, a potent PARPi, with enzalutamide, a strong androgen receptor (AR) antagonist. The combination of these two drugs was evaluated by the TALAPRO-2 trial, demonstrating significant improvement in radiographic progression-free survival (rPFS) in metastatic castration-resistant prostate cancer (mCRPC) patients, particularly those with Homologous Recombination Repair (HRR) gene mutations such as BRCA1/2.

EXPERT OPINION

Emerging biomarkers like TMPRSS2-ERG and RB1 gene mutations have been recently reported as potential predictors of clinical outcome in the TALAPRO-2 all-comers population. Genomic markers for homologous recombination deficiency (HRD) are other potential drivers of response to PARPi/ARPI combination. Further investigation is needed to refine treatment strategies, including targeting non-HRR mutations, and to expand the role of this combination therapy in earlier stages of prostate cancer.

摘要

引言

前列腺癌(PCa)是全球男性中第二常见的癌症诊断类型,晚期预后较差。治疗策略不断发展,包括使用雄激素受体途径抑制剂(ARPIs)和聚(ADP-核糖)聚合酶抑制剂(PARPis)。

涵盖领域

本综述评估了强效PARPi他拉唑帕尼与强效雄激素受体(AR)拮抗剂恩杂鲁胺联合使用的临床疗效、安全性和未来潜力。这两种药物的联合使用通过TALAPRO-2试验进行了评估,结果表明转移性去势抵抗性前列腺癌(mCRPC)患者,尤其是那些具有同源重组修复(HRR)基因突变如BRCA1/2的患者,在影像学无进展生存期(rPFS)方面有显著改善。

专家意见

最近有报道称,新兴生物标志物如TMPRSS2-ERG和RB1基因突变是TALAPRO-2所有受试者群体临床结果的潜在预测指标。同源重组缺陷(HRD)的基因组标志物是对PARPi/ARPI联合治疗反应的其他潜在驱动因素。需要进一步研究以完善治疗策略,包括针对非HRR突变,并扩大这种联合治疗在前列腺癌早期阶段的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验