医学
奥拉帕尼
卡巴齐塔塞尔
前列腺癌
多西紫杉醇
肿瘤科
雄激素剥夺疗法
内科学
PARP抑制剂
化疗
恩扎鲁胺
癌症
雄激素受体
聚ADP核糖聚合酶
聚合酶
基因
生物化学
化学
作者
Andrea Marchetti,Elisa Tassinari,Matteo Rosellini,Alessandro Rizzo,Francesco Massari,Veronica Mollica
标识
DOI:10.1080/17512433.2023.2181783
摘要
Introduction Androgen deprivation therapy (ADT) plus Androgen Receptor Target Agents (ARTAs) or docetaxel are the actual standard of care in prostate cancer (PC). Several therapeutic options are available for pretreated patients: cabazitaxel, olaparib, and rucaparib for BRCA mutations, Radium-223 for selected patients with symptomatic bone metastasis, sipuleucel T, and 177 LuPSMA-617.Areas covered This review the new potential therapeutic approaches and the most impacting recent published trials to provide an overview on the future management of PC.Expert opinion Currently, there is a growing interest in the potential role of triplet therapies encompassing ADT, chemotherapy, and ARTAs. These strategies, explored in different settings, appeared to be particularly promising in metastatic hormone-sensitive PC. Recent trials investigating ARTAs plus poly(adenosine diphosphate–ribose) polymerase (PARPi) inhibitor provided helpful insights for patients with metastatic castration resistant disease, regardless of homologous recombination genes status. Otherwise, the publication of the complete data is awaited, and more evidence is required. In advanced settings, several combination approaches are under investigation, to date with contradictory results, such as immunotherapy plus PARPi or chemotherapy. The radionuclide 177Lu-PSMA-617 proved successful outcomes in pretreated mCRPC patients. Additional studies will better clarify the appropriate candidates to each strategy and the correct treatments’ sequence.
科研通智能强力驱动
Strongly Powered by AbleSci AI