Department of Medical Oncology, Santa Chiara Hospital, Trento, Italy.
Department of Radiological, Oncological and Anatomo-Pathological Sciences, La Sapienza University, Rome, Italy.
Cancer Biother Radiopharm. 2021 Jun;36(5):391-396. doi: 10.1089/cbr.2020.4442. Epub 2021 Mar 25.
The retrospective studies that have so far described the outcomes of the sequential use of life-prolonging agents (LPAs) did not include metastatic castration-resistant prostate cancer (mCRPC) patients who received radium-223 (Ra) as part of their treatment. Consequently, it is not known whether including Ra in the therapeutic sequence has an impact on cumulative survival. The aim of this study was to evaluate this impact by comparing the cumulative overall survival (OS) in two series of mCRPC patients sequentially treated with two or three LPAs after first-line docetaxel (DOC), including Ra and not. The authors retrospectively reviewed the records of mCRPC patients with bone involvement alone who received two or three LPAs (including Ra) after first-line DOC. The control group was a contemporary series of mCRPC patients with bone involvement alone treated with sequences of two or three LPAs other than Ra after first-line DOC. Median cumulative OS was 40.6 months in the Ra group of 78 patients and 36.2 months in the non-Ra group of 186 patients ( = 0.08). OS outcomes were significantly influenced by the number of treatment lines, and baseline Eastern Cooperative Oncology Group performance status (PS) and prostate-specific antigen levels. To the best of the authors' knowledge, this is the first study designed to evaluate the impact of introducing Ra in the treatment sequences for mCRPC patients, and the results show that its use does not negatively affect cumulative OS.
迄今为止,描述序贯使用延长生命药物(LPAs)的结果的回顾性研究并未包括接受镭-223(Ra)作为治疗一部分的转移性去势抵抗性前列腺癌(mCRPC)患者。因此,尚不清楚在治疗方案中加入 Ra 是否会对累积生存率产生影响。本研究旨在通过比较接受一线多西他赛(DOC)治疗后序贯使用两种或三种 LPAs(包括 Ra)的两组 mCRPC 患者的累积总生存期(OS)来评估这种影响。作者回顾性分析了仅接受一线 DOC 治疗后接受两种或三种 LPAs(包括 Ra)治疗的 mCRPC 患者的记录。对照组为单独接受一线 DOC 治疗后接受两种或三种除 Ra 以外的 LPAs 序贯治疗的 mCRPC 患者。78 例 Ra 组患者的中位累积 OS 为 40.6 个月,186 例非 Ra 组患者的中位累积 OS 为 36.2 个月( = 0.08)。OS 结果受治疗线数、基线东部肿瘤协作组表现状态(PS)和前列腺特异性抗原水平的显著影响。据作者所知,这是第一项旨在评估在 mCRPC 患者的治疗方案中引入 Ra 的影响的研究,结果表明其使用不会对累积 OS 产生负面影响。