Department of Radiation Oncology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Department of Urology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Prostate Cancer Prostatic Dis. 2022 Mar;25(1):126-128. doi: 10.1038/s41391-021-00432-2. Epub 2021 Aug 16.
While multiple randomized trials have evaluated the benefit of radiation therapy (RT) dose escalation and the use and prolongation of androgen deprivation therapy (ADT) in the treatment of prostate cancer, few studies have evaluated the relative benefit of either form of treatment intensification with each other. Many trials have included treatment strategies that incorporate either high or low dose RT, or short-term or long-term ADT (STADT or LTADT), in one or more trial arms. We sought to compare different forms of treatment intensification of RT in the context of localized prostate cancer.
Using preferred reporting items for systemic reviews and meta-analyses (PRISMA) guidelines, we collected over 40 phases III clinical trials comparing different forms of RT for localized prostate cancer. We performed a meta-regression of 40 individual trials with 21,429 total patients to allow a comparison of the rates and cumulative proportions of 5-year overall survival (OS), prostate cancer-specific mortality (PCSM), and distant metastasis (DM) for each treatment arm of every trial.
Dose-escalation either in the absence or presence of STADT failed to significantly improve any 5-year outcome. In contrast, adding LTADT to low dose RT significantly improved 5-year PCSM (Odds ratio [OR] 0.34, 95% confidence interval [CI] 0.22-0.54, p < 0.001) and DM (OR 0.35, 95% CI 0.20-0.63. p < 0.001) over low dose RT alone. Adding STADT also significantly improved 5-year PCSM over low dose RT alone (OR 0.55, 95% CI 0.41-0.75, p < 0.001).
While limited by between-study heterogeneity and a lack of individual patient data, this meta-analysis suggests that adding ADT, versus increasing RT dose alone, offers a more consistent improvement in clinical endpoints.
虽然多项随机试验已经评估了放射治疗(RT)剂量递增以及雄激素剥夺治疗(ADT)的应用和延长在前列腺癌治疗中的益处,但很少有研究评估这两种治疗强化形式之间的相对益处。许多试验包括了在一个或多个试验臂中采用高剂量或低剂量 RT,或短期或长期 ADT(STADT 或 LTADT)的治疗策略。我们试图在局部前列腺癌的背景下比较 RT 的不同形式的治疗强化。
我们使用系统评价和荟萃分析的首选报告项目(PRISMA)指南,收集了 40 项比较局部前列腺癌不同形式 RT 的 III 期临床试验。我们对 40 项单独试验进行了荟萃回归分析,共有 21429 名患者,以比较每个试验的每个治疗臂的 5 年总生存率(OS)、前列腺癌特异性死亡率(PCSM)和远处转移(DM)的发生率和累积比例。
在没有或存在 STADT 的情况下,剂量递增未能显著改善任何 5 年的结果。相比之下,将 LTADT 加入低剂量 RT 显著改善了 5 年的 PCSM(比值比 [OR] 0.34,95%置信区间 [CI] 0.22-0.54,p < 0.001)和 DM(OR 0.35,95% CI 0.20-0.63,p < 0.001),而不是单独使用低剂量 RT。单独使用低剂量 RT 时,添加 STADT 也显著改善了 5 年的 PCSM(OR 0.55,95% CI 0.41-0.75,p < 0.001)。
尽管受到研究间异质性和缺乏个体患者数据的限制,但这项荟萃分析表明,与单独增加 RT 剂量相比,添加 ADT 提供了更一致的临床终点改善。