Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.
Cancer. 2013 Aug 15;119(16):3020-6. doi: 10.1002/cncr.28145. Epub 2013 May 29.
Use of progression-free survival (PFS) as a clinical trial endpoint in first-line treatment of patients with metastatic urothelial carcinoma (UC) is attractive, but would be enhanced by establishing a correlation between PFS and overall survival (OS).
Data was pooled from 7 phase 2 and 3 trials evaluating cisplatin-based chemotherapy in metastatic UC. An independent cohort of patients enrolled on a phase 3 trial was used for external validation. Landmark analyses for progression at 6 and 9 months after treatment initiation were performed to minimize lead-time bias. A proportional hazards model was used to assess the utility of PFS for predicting OS.
A total of 364 patients were included in the initial cohort. The median PFS was 8.21 months (95% confidence interval = 7.43, 8.39) and the median OS was 13.50 months (95% confidence interval = 11.80, 15.67). In the landmark analysis, the median OS for patients who progressed at 6 months was 3.87 months compared with 15.06 months for those patients who did not progress (P < .0001) and the median OS for patients who progressed at 9 months was 5.65 months compared with 21.39 months for those patients who did not progress (P < .0001). A Fleischer model demonstrated a statistically significant dependent correlation between PFS and OS. The findings were externally validated in an independent cohort.
PFS at 6 and 9 months predicted OS in this analysis of patients with metastatic UC treated with first-line cisplatin-based chemotherapy and could potentially serve as endpoints in (randomized) phase 2 trials to screen the activity of novel regimens.
在转移性尿路上皮癌(UC)的一线治疗中,将无进展生存期(PFS)用作临床试验终点很有吸引力,但如果能建立 PFS 与总生存期(OS)之间的相关性,则会有所增强。
对评估转移性 UC 患者使用顺铂为基础的化疗的 7 项 2 期和 3 期临床试验的数据进行了汇总。还使用 3 期试验中入组的独立患者队列进行外部验证。进行治疗开始后 6 个月和 9 个月时的进展里程碑分析,以尽量减少领先时间偏倚。使用比例风险模型评估 PFS 预测 OS 的效用。
初始队列共纳入 364 例患者。中位 PFS 为 8.21 个月(95%置信区间=7.43,8.39),中位 OS 为 13.50 个月(95%置信区间=11.80,15.67)。在里程碑分析中,在 6 个月时进展的患者的中位 OS 为 3.87 个月,而未进展的患者为 15.06 个月(P<0.0001);在 9 个月时进展的患者的中位 OS 为 5.65 个月,而未进展的患者为 21.39 个月(P<0.0001)。弗莱舍模型显示 PFS 与 OS 之间存在统计学显著的依存相关性。这些发现在外独立队列中得到了验证。
本分析中,在接受一线以顺铂为基础的化疗治疗的转移性 UC 患者中,6 个月和 9 个月的 PFS 预测了 OS,并且有可能作为(随机)2 期试验的终点,以筛选新方案的活性。