Relationship between Treatment Effects on Progression-Free Survival and Overall Survival in Multiple Myeloma: A Systematic Review and Meta-Analysis of Published Clinical Trial Data

被引:26
|
作者
Cartier, Shannon [1 ]
Zhang, Bin [2 ]
Rosen, Virginia M. [1 ]
Zarotsky, Victoria [1 ]
Bartlett, J. Blake [2 ]
Mukhopadhyay, Pralay [2 ]
Wagner, Samuel [2 ]
Davis, Catherine [2 ]
机构
[1] Optum, Eden Prairie, MN USA
[2] Bristol Myers Squibb Co, Princeton, NJ 08540 USA
关键词
Multiple myeloma; Progression-free survival; Overall survival; Surrogate; Correlation; SURROGATE END-POINTS; PREDNISONE PLUS THALIDOMIDE; RANDOMIZED CONTROLLED-TRIAL; PEGYLATED LIPOSOMAL DOXORUBICIN; METASTATIC COLORECTAL-CANCER; ELDERLY-PATIENTS; PHASE-III; 1ST-LINE CHEMOTHERAPY; MELPHALAN; DEXAMETHASONE;
D O I
10.1159/000375392
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Demonstrating improved overall survival (OS) with new multiple myeloma (MM) treatments is becoming difficult because of extended survival, so progression-free survival (PFS) is commonly used as a surrogate endpoint for OS. We evaluated PFS as a potential surrogate for OS by examining whether observed treatment effects on PFS are positively associated with treatment effects on OS in MM. Methods: A systematic literature review identified 21 randomized control trials reporting hazard ratios (HRs) for treatment effects on PFS and OS. Pearson's r estimated the relationship between HRs (HRpFs and HRos), and between log-transformed HRs (log(HRpFs) and log(HRos)). R2 values were estimated from linear regression models of the HR and the log(HR) relationships. Sensitivity and subgroup analyses examined the robustness of the HR findings. Results: Positive correlations were found between HRpFs and HRos (r = 0.82; p <0.0001) and between log(HRpFs) and log(HRos) (r = 0.80; p <0.0001). Linear regression models produced R2 values of 0.67 and 0.63 when regressing HRos on HRpFs, and log(HRos) on log(HRpFs), respectively. Sensitivity analyses supported the HR findings. Conclusion: This analysis provides evidence for a positive association between treatment effects on PFS and OS. Studies involving patient level data are necessary to confirm whether PFS is a valid surrogate for OS in MM.
引用
收藏
页码:88 / 94
页数:7
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