Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Wahringer Gurtel 18-20, 1090, Vienna, Austria.
Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Int J Clin Oncol. 2024 Jun;29(6):716-725. doi: 10.1007/s10147-024-02485-4. Epub 2024 Apr 6.
Triplet therapy, androgen receptor signaling inhibitors (ARSIs) plus docetaxel plus androgen-deprivation therapy (ADT), is a novel guideline-recommended treatment for metastatic hormone-sensitive prostate cancer (mHSPC). However, the optimal selection of the patient most likely to benefit from triplet therapy remains unclear.
We performed a systematic review, meta-analysis, and network meta-analysis to assess the oncologic benefit of triplet therapy in mHSPC patients stratified by disease volume and compare them with doublet treatment regimens. Three databases and meeting abstracts were queried in March 2023 for randomized controlled trials (RCTs) evaluating patients treated with systemic therapy for mHSPC stratified by disease volume. Primary interests of measure were overall survival (OS). We followed the PRISMA guideline and AMSTAR2 checklist.
Overall, eight RCTs were included for meta-analyses and network meta-analyses (NMAs). Triplet therapy outperformed docetaxel plus ADT in terms of OS in both patients with high-(pooled HR: 0.73, 95%CI 0.64-0.84) and low-volume mHSPC (pooled HR: 0.71, 95%CI 0.52-0.97). There was no statistically significant difference between patients with low- vs. high-volume in terms of OS benefit from adding ARSI to docetaxel plus ADT (p = 0.9). Analysis of treatment rankings showed that darolutamide plus docetaxel plus ADT (90%) had the highest likelihood of improved OS in patients with high-volume disease, while enzalutamide plus ADT (84%) had the highest in with low-volume disease.
Triplet therapy improves OS in mHSPC patients compared to docetaxel-based doublet therapy, irrespective of disease volume. However, based on treatment ranking, triplet therapy should preferably be considered for patients with high-volume mHSPC while those with low-volume are likely to be adequately treated with ARSI + ADT.
三联疗法(雄激素受体信号抑制剂[ARSIs]联合多西他赛和雄激素剥夺治疗[ADT])是一种新的指南推荐的治疗转移性激素敏感前列腺癌(mHSPC)的方法。然而,哪种患者最有可能从三联疗法中获益仍不清楚。
我们进行了系统评价、荟萃分析和网络荟萃分析,以评估三联疗法在 mHSPC 患者中的肿瘤学获益,并按疾病体积对其与双药治疗方案进行比较。2023 年 3 月,我们检索了三个数据库和会议摘要,以评估按疾病体积分层的接受系统治疗的 mHSPC 患者的随机对照试验(RCT)。主要测量指标是总生存期(OS)。我们遵循 PRISMA 指南和 AMSTAR2 清单。
共有 8 项 RCT 被纳入进行荟萃分析和网络荟萃分析(NMA)。三联疗法在高体积(汇总 HR:0.73,95%CI 0.64-0.84)和低体积 mHSPC(汇总 HR:0.71,95%CI 0.52-0.97)患者中的 OS 均优于多西他赛加 ADT。低体积与高体积患者在添加 ARSI 至多西他赛加 ADT 后 OS 获益方面无统计学差异(p=0.9)。治疗排序分析显示,达罗他胺联合多西他赛加 ADT(90%)在高体积疾病患者中具有改善 OS 的最高可能性,而恩扎卢胺联合 ADT(84%)在低体积疾病患者中具有最高可能性。
与多西他赛为基础的双药治疗相比,三联疗法可提高 mHSPC 患者的 OS,与疾病体积无关。然而,根据治疗排序,三联疗法可能更适合高体积 mHSPC 患者,而低体积患者可能通过 ARSI+ADT 得到充分治疗。