Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; Department of Urology, Medical University of Silesia, Zabrze, Poland.
Eur Urol. 2022 Dec;82(6):584-598. doi: 10.1016/j.eururo.2022.08.002. Epub 2022 Aug 19.
Recent randomized controlled trials (RCTs) examined the role of adding androgen receptor signaling inhibitors (ARSIs), including abiraterone acetate (ABI), apalutamide, darolutamide (DAR), and enzalutamide (ENZ), to docetaxel (DOC) and androgen deprivation therapy (ADT) in patients with metastatic hormone-sensitive prostate cancer (mHSPC).
To analyze the oncologic benefit of triplet combination therapies using ARSI + DOC + ADT, and comparing them with available treatment regimens in patients with mHSPC.
Three databases and meetings abstracts were queried in April 2022 for RCTs analyzing patients treated with first-line combination systemic therapy for mHSPC. The primary interests of measure were overall survival (OS) and progression-free survival (PFS). Subgroup analyses were conducted to assess the differential outcomes in patients with low- and high-volume disease as well as de novo and metachronous metastasis.
Overall, 11 RCTs were included for meta-analyses and network meta-analyses (NMAs). We found that the triplet combinations outperformed DOC + ADT in terms of OS (pooled hazard ratio [HR]: 0.74, 95% confidence interval [CI]: 0.65-0.84) and PFS (pooled HR: 0.49, 95% CI: 0.42-0.58). There was no statistically significant difference between patients with low- and high-volume disease in terms of an OS benefit from adding an ARSI to DOC +ADT (both HR: 0.79; p = 1). Based on NMAs, triplet therapy also outperformed ARSI + ADT in terms of OS (DAR + DOC + ADT: pooled HR: 0.74, 95% CI: 0.55-0.99) and PFS (ABI + DOC + ADT: HR: 0.68, 95% CI: 0.51-0.91, and ENZ + DOC + ADT: HR: 0.70, 95% CI: 0.53-0.93). An analysis of treatment ranking among de novo mHSPC patients showed that triplet therapy had the highest likelihood of improved OS in patients with high-volume disease; however, doublet therapy using ARSI + ADT had the highest likelihood of improved OS in patients with low-volume disease.
We found that the triplet combination therapy improves survival endpoints in mHSPC patients compared with currently available doublet treatment regimens. Our findings need to be confirmed in further head-to-head trials with longer follow-up and among various patient populations.
Our study suggests that triplet therapy with androgen receptor signaling inhibitor, docetaxel, androgen deprivation therapy prolongs survival in patients with metastatic hormone-sensitive prostate cancer compared with the current standard doublet therapy.
最近的随机对照试验(RCT)研究了在转移性激素敏感前列腺癌(mHSPC)患者中添加雄激素受体信号抑制剂(ARSIs),包括醋酸阿比特龙(ABI)、阿帕鲁胺、达罗他胺(DAR)和恩扎卢胺(ENZ),联合多西他赛(DOC)和雄激素剥夺疗法(ADT)的作用。
分析使用 ARSI+DOC+ADT 的三联组合疗法的肿瘤学益处,并将其与 mHSPC 患者的现有治疗方案进行比较。
2022 年 4 月,对三个数据库和会议摘要进行了检索,以分析接受一线联合系统治疗 mHSPC 的患者的 RCT。主要的测量指标是总生存期(OS)和无进展生存期(PFS)。进行了亚组分析,以评估低容量和高容量疾病以及新发和继发转移患者的不同结局。
总体而言,有 11 项 RCT 被纳入进行荟萃分析和网络荟萃分析(NMAs)。我们发现三联组合在 OS(汇总风险比 [HR]:0.74,95%置信区间 [CI]:0.65-0.84)和 PFS(汇总 HR:0.49,95% CI:0.42-0.58)方面优于 DOC+ADT。在添加 ARSI 对 DOC+ADT 的 OS 获益方面,低容量和高容量疾病患者之间没有统计学意义的差异(两者的 HR:0.79;p=1)。基于 NMAs,三联疗法在 OS(DAR+DOC+ADT:汇总 HR:0.74,95% CI:0.55-0.99)和 PFS(ABI+DOC+ADT:HR:0.68,95% CI:0.51-0.91,和 ENZ+DOC+ADT:HR:0.70,95% CI:0.53-0.93)方面也优于 ARSI+ADT。对新发 mHSPC 患者的治疗排名分析表明,在高容量疾病患者中,三联疗法有提高 OS 的最高可能性;然而,在低容量疾病患者中,使用 ARSI+ADT 的双联疗法有提高 OS 的最高可能性。
我们发现,与目前可用的双联治疗方案相比,三联组合疗法可改善 mHSPC 患者的生存终点。我们的研究结果需要在具有更长随访时间和不同患者人群的进一步头对头试验中得到证实。
我们的研究表明,与目前的标准双联治疗相比,雄激素受体信号抑制剂、多西他赛和雄激素剥夺疗法的三联疗法可延长转移性激素敏感前列腺癌患者的生存期。