Royal Free London NHS Foundation Trust and UCL Division of Surgery and Interventional Science, London, UK.
Netherlands Cancer Institute, Amsterdam, the Netherlands.
BJU Int. 2022 Jul;130(1):68-75. doi: 10.1111/bju.15625. Epub 2021 Nov 24.
To analyse if exposure to sunitinib in the Immediate Surgery or Surgery After Sunitinib Malate in Treating Patients With Metastatic Kidney Cancer (SURTIME) trial, which investigated opposite sequences of cytoreductive nephrectomy (CN) and systemic therapy, is associated with the overall survival (OS) benefit observed in the deferred CN arm.
A post hoc analysis of SURTIME trial data. Variables analysed included number of patients receiving sunitinib, time from randomisation to start sunitinib, overall response rate by Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1, and duration of drug exposure and dose in the intention-to-treat population of the immediate and deferred arm. Descriptive methods and 95% confidence-intervals (CI) were used.
In the deferred arm, 97.7% (95% CI 89.3-99.6%; n = 48) received sunitinib vs 80% (95% CI 66.9-88.7%, n = 40) in the immediate arm. Following immediate CN, 19.6% progressed 4 weeks after CN and the median time to start sunitinib was 39.5 vs 4.5 days in the deferred arm. At week 16, 46.0% had progressed at metastatic sites in the immediate CN arm vs 32.7% in the deferred arm. Sunitinib dose reductions, escalations and interruptions were not statistically significantly different between arms. Among patients who received sunitinib in the immediate or deferred arm the median total sunitinib treatment duration was 172.5 vs 248 days. Reduction of target lesions was more profound in the deferred arm.
In comparison to the deferred CN approach, immediate CN impairs administration, onset, and duration of sunitinib. Starting with systemic therapy leads to early and more profound disease control and identification of progression prior to planned CN, which may have contributed to the observed OS benefit.
分析在 SURTIME 试验中,接受舒尼替尼治疗的患者是否与延迟肾切除术(CN)组观察到的总生存期(OS)获益相关,该试验研究了相反的细胞减灭性肾切除术(CN)和系统治疗顺序。
对 SURTIME 试验数据进行事后分析。分析的变量包括接受舒尼替尼治疗的患者数量、从随机分组到开始舒尼替尼治疗的时间、根据实体瘤反应评估标准 1.1(RECIST)版评估的总体缓解率以及意向治疗人群中直接和延迟臂的药物暴露时间和剂量。使用描述性方法和 95%置信区间(CI)。
在延迟臂,97.7%(95%CI 89.3-99.6%;n=48)接受了舒尼替尼治疗,而直接臂为 80%(95%CI 66.9-88.7%,n=40)。在直接 CN 后,19.6%的患者在 CN 后 4 周进展,延迟臂开始舒尼替尼治疗的中位时间为 39.5 天,而直接臂为 4.5 天。在第 16 周,直接 CN 组中有 46.0%的转移性部位进展,而延迟臂为 32.7%。直接和延迟臂之间的舒尼替尼剂量减少、增加和中断没有统计学上的显著差异。在接受舒尼替尼治疗的直接或延迟臂患者中,中位总舒尼替尼治疗持续时间分别为 172.5 天和 248 天。延迟臂的靶病灶缩小更为明显。
与延迟 CN 方法相比,直接 CN 会影响舒尼替尼的给药、开始和持续时间。首先进行系统治疗可更早、更深入地控制疾病,并在计划进行 CN 之前确定进展,这可能促成了观察到的 OS 获益。