Pharmalytics Group, Vancouver, British Columbia, Canada.
Curr Med Res Opin. 2024 Oct;40(10):1741-1752. doi: 10.1080/03007995.2024.2395435. Epub 2024 Aug 27.
To review the literature to outline findings from clinical trials assessing interventions for metastatic castration-resistant prostate cancer (mCRPC) in patients who have progressed on androgen receptor-axis-targeted (ARAT) therapies.
A systematic literature review was performed to identify trials that assessed the efficacy and safety of interventions used in patients that progressed on prior ARAT therapies. A literature search was conducted using the OVID platform that searched the EMBASE, MEDLINE, and CENTRAL bibliographic databases.
Of the 10,114 citations identified, a total of 36 studies representing 33 unique trials were included in the review. Of the 33 trials, 21 were randomized controlled trials and 12 were single-arm trials. A total of 11 were phase III trials, 13 were phase II trials, and 2 were phase I trials. The majority of included trials were open-label ( = 29) and the remaining were double-blind ( = 4). A total of 16 trials evaluated ARAT based therapies, 7 trials evaluated taxane-based treatments, 10 trials evaluated PARP inhibitors, 8 trials evaluated immunotherapies, and 8 trials evaluated other therapies (i.e. cabozantinib, mitoxantrone, radium-223,[Lu-177]-PNT2002,Lu-PSMA-617, samotolisib).
This systematic review demonstrated there are limited effective treatment options in this patient population. Unlike other cancer types, immunotherapy agents appear to provide little to no benefit. Conversely, agents such as taxane-based chemotherapy (e.g. cabazitaxel) and radionuclide therapy provide the most value in this patient population. Further research is needed to explore new therapies in this disease area and to optimize existing treatment strategies with more effective combination therapies.
本文系统地回顾了评估转移性去势抵抗性前列腺癌(mCRPC)患者在接受雄激素受体轴靶向(ARAT)治疗后进展时干预措施的临床试验结果。
通过使用 OVID 平台检索 EMBASE、MEDLINE 和 CENTRAL 书目数据库,进行了系统的文献检索,以确定评估在接受先前 ARAT 治疗后进展的患者中使用干预措施的疗效和安全性的试验。
在确定的 10,114 条引文,共有 36 项研究(代表 33 项独特的试验)纳入本综述。在 33 项试验中,21 项为随机对照试验,12 项为单臂试验。其中,11 项为 III 期试验,13 项为 II 期试验,2 项为 I 期试验。大多数纳入的试验为开放性( = 29),其余为双盲( = 4)。共有 16 项试验评估了基于 ARAT 的治疗,7 项试验评估了紫杉烷类治疗,10 项试验评估了 PARP 抑制剂,8 项试验评估了免疫疗法,8 项试验评估了其他疗法(即卡博替尼、米托蒽醌、镭-223,[Lu-177]-PNT2002,Lu-PSMA-617,samatolisib)。
本系统评价表明,在该患者群体中,有效的治疗选择有限。与其他癌症类型不同,免疫治疗药物似乎几乎没有获益。相反,紫杉烷类化疗(如卡巴他赛)和放射性核素治疗等药物在该患者群体中提供了最大的价值。需要进一步研究探索该疾病领域的新疗法,并通过更有效的联合治疗方案优化现有治疗策略。