Ghali Fady, Zhao Yibai, Patel Devin, Jewell Teresa, Yu Evan Y, Grivas Petros, Montgomery R Bruce, Gore John L, Etzioni Ruth B, Wright Jonathan L
Department of Urology, University of Washington School of Medicine, Seattle, WA, USA.
Biostatistics Program, Fred Hutch Cancer Center, Seattle, WA, USA.
Eur Urol Open Sci. 2022 Dec 15;47:58-64. doi: 10.1016/j.euros.2022.11.003. eCollection 2023 Jan.
Surrogate endpoints (SEs), such as progression-free survival (PFS) and objective response rate (ORR), are frequently used in clinical trials. The relationship between SEs and overall survival (OS) has not been well described in metastatic urothelial cancer (MUC).
We evaluated trial-level data to assess the relationship between SEs and OS. We hypothesize a moderate surrogacy relationship between both PFS and ORR with OS.
We systematically reviewed phase 2/3 trials in MUC with two or more treatment arms, and report PFS and/or ORR, and OS.
Linear regression was performed, and the coefficient of determination (R) and surrogate threshold effect (STE) estimate were determined between PFS/ORR and OS.
Of 3791 search results, 59 trials and 62 comparisons met the inclusion criteria. Of the 53 trials that reported PFS, 31 (58%) reported proportional hazard regression for PFS and OS. Linear regression across trials demonstrated an R of 0.60 between hazard ratio (HR) for PFS (HR) and HR for OS (HR), and an STE of 0.41. Linear regression of ΔPFS (median PFS in months of the treatment arm - that of the control arm) and ΔOS demonstrated an R of 0.12 and an STE of 14.1 mo. Thirty trials reported ORRs. Linear regression for ORR and HR among all trials found an R of 0.08; an STE of 95% was not reached at any value and ΔORR and HR similarly demonstrated a poor correlation with an R value of 0.03.
PFS provides only a moderate level of surrogacy for OS; An HR of ≤0.41 provides 95% confidence of OS improvement. ORR is weakly correlated with OS and should be de-emphasized in MUC clinical trials. When PFS is discussed, proportional hazard regression should be reported.
We examined the relationship between surrogate endpoints, common outcomes in clinical trials, with survival in urothelial cancer trials. Progression-free survival is moderately correlated, while objective response rate had a poor correlation with survival and should be de-emphasized as a primary endpoint.
替代终点(SEs),如无进展生存期(PFS)和客观缓解率(ORR),在临床试验中经常被使用。在转移性尿路上皮癌(MUC)中,SEs与总生存期(OS)之间的关系尚未得到充分描述。
我们评估了试验水平的数据,以评估SEs与OS之间的关系。我们假设PFS和ORR与OS之间存在中等程度的替代关系。
设计、设置和参与者:我们系统回顾了MUC中具有两个或更多治疗组的2/3期试验,并报告了PFS和/或ORR以及OS。
进行线性回归,并确定PFS/ORR与OS之间的决定系数(R)和替代阈值效应(STE)估计值。
在3791个搜索结果中,59项试验和62项比较符合纳入标准。在报告PFS的53项试验中,31项(58%)报告了PFS和OS的比例风险回归。跨试验的线性回归显示,PFS的风险比(HR)与OS的HR之间的R为0.60,STE为0.41。ΔPFS(治疗组的中位PFS月数 - 对照组的中位PFS月数)与ΔOS的线性回归显示R为0.12,STE为14.1个月。30项试验报告了ORR。所有试验中ORR与HR的线性回归发现R为0.08;在任何值下均未达到95%的STE,并且ΔORR与HR同样显示出较差的相关性,R值为0.03。
PFS仅为OS提供中等程度的替代水平;HR≤0.41提供了95%的OS改善置信度。ORR与OS的相关性较弱,在MUC临床试验中应不再强调。当讨论PFS时,应报告比例风险回归。
我们研究了临床试验中常见的替代终点与尿路上皮癌试验中的生存期之间的关系。无进展生存期具有中等相关性,而客观缓解率与生存期的相关性较差,应不再强调将其作为主要终点。