Genitourinary Malignancy Branch, National Cancer Institute, Bethesda, MD, USA.
GU Medical Oncology, Inova Schar Cancer Institute, Fairfax, VA, USA.
Expert Rev Anticancer Ther. 2023 Jun;23(6):625-631. doi: 10.1080/14737140.2023.2208352. Epub 2023 May 2.
Prostate cancer treatment has rapidly evolved in the past few years. Androgen deprivation therapy has been the backbone of treatment for locally advanced and metastatic prostate cancer, but incremental benefits in survival have been shown by adding androgen-receptor pathway inhibitors (ARPI) across various spectrums of disease state. In addition, docetaxel chemotherapy remains the first-line chemotherapy regimen available with survival benefits shown with triplet therapy in those who are chemotherapy eligible. However, disease progression remains inevitable and novel agents such as radioligand therapy with lutetium have shown improvement in survival.
This review discusses the pivotal trials that led to the U.S. FDA approval of agents utilized in metastatic prostate cancer and explores the use of novel agents including prostate-specific membrane antigen-targeting agents, radioligands, cell-based therapy, chimeric antigen receptor T-cell, BiTE, and antibody drug conjugates.
Treatment landscape for metastatic castrate-resistant prostate cancer (mCRPC) has evolved beyond additional agents with ARPI and/or docetaxel, including other treatments with sipuleucel-T, radium, cabazitaxel, PARP inhibitors, and lutetium, which have specific indications and roles in sequencing. Novel therapies remain critically needed after progression from lutetium.
在过去的几年中,前列腺癌的治疗方法迅速发展。去势治疗一直是局部晚期和转移性前列腺癌治疗的基础,但在各种疾病状态下,添加雄激素受体通路抑制剂(ARPI)已显示出生存获益的递增。此外,多西他赛化疗仍然是可用的一线化疗方案,在有化疗适应证的患者中,三联疗法显示出生存获益。然而,疾病进展仍然不可避免,新型药物如镥放射性配体治疗在生存方面显示出改善。
本文综述了导致美国 FDA 批准用于转移性前列腺癌的药物的关键试验,并探讨了新型药物的使用,包括前列腺特异性膜抗原靶向药物、放射性配体、基于细胞的治疗、嵌合抗原受体 T 细胞、BiTE 和抗体药物偶联物。
去势抵抗性转移性前列腺癌(mCRPC)的治疗领域已经超越了 ARPI 和/或多西他赛的附加药物,包括其他治疗方法如 sipuleucel-T、镭、卡巴他赛、PARP 抑制剂和镥,这些药物在特定情况下具有特定的适应证和作用。在使用镥治疗后,仍然迫切需要新的治疗方法。