Medical Oncology Department, Santa Chiara Hospital, Trento, Italy.
Medical Oncology Department, University Medical Centre, Leiden, the Netherlands.
Clin Genitourin Cancer. 2020 Feb;18(1):69-76.e4. doi: 10.1016/j.clgc.2019.09.010. Epub 2019 Sep 27.
The sequential use of a number of new agents (NAs) have improved the overall survival (OS) of patients with metastatic castration-resistant prostate cancer whose disease progresses after docetaxel (DOC) treatment. The aim of this study was to assess the cumulative survival outcomes of different sequencing strategies by evaluating the individual data from published studies of patients treated with a post-DOC treatment sequence of 2 NAs.
The patients' individual data were analyzed to investigate whether different sequencing strategies lead to differences in OS.
We analyzed the data of 1099 evaluable patients. Among the patients treated with a second-line new hormone agent (NHA), median OS from the start of third-line treatment was significantly longer in the patients treated with cabazitaxel (CABA) than in those treated with abiraterone acetate or enzalutamide. Median cumulative OS (cumOS) from the start of second-line treatment was 21.1 months in the patients who received NHA then NHA, 22.1 months in those who received NHA then CABA, and 21.0 months in those who received CABA then NHA. Among the patients with a second-line progression-free survival of ≥6 months, median cumOS was significantly longer in patients who received CABA-including sequences than in those treated with NHA then NHA sequences (29.5 vs. 24.8 months; P = .03).
Our findings suggest that the sequential use of NAs with different mechanisms of action improves cumOS regardless of the order in which they are administered, thus supporting the hypothesis of cross-resistance between the 2 NHAs.
在多西他赛(DOC)治疗后疾病进展的转移性去势抵抗性前列腺癌(mCRPC)患者中,一系列新型药物(NAs)的序贯使用提高了总生存期(OS)。本研究旨在通过评估接受 DOC 后治疗序贯使用 2 种 NAs 的患者的个体数据,评估不同序贯策略的累积生存结果。
分析患者的个体数据,以评估不同的序贯策略是否导致 OS 存在差异。
我们分析了 1099 例可评估患者的数据。在接受二线新型激素治疗(NHA)的患者中,从三线治疗开始的中位 OS 明显长于醋酸阿比特龙或恩扎卢胺治疗的患者。从二线治疗开始的中位累积 OS(cumOS)在接受 NHA 然后 NHA 的患者中为 21.1 个月,在接受 NHA 然后 CABA 的患者中为 22.1 个月,在接受 CABA 然后 NHA 的患者中为 21.0 个月。在二线无进展生存时间≥6 个月的患者中,接受包含 CABA 的序贯治疗的患者的中位 cumOS 明显长于接受 NHA 然后 NHA 序贯治疗的患者(29.5 比 24.8 个月;P =.03)。
我们的研究结果表明,无论顺序如何,不同作用机制的 NAs 的序贯使用都可以提高 cumOS,从而支持了两种 NHA 之间交叉耐药的假说。