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