4.3 Review

Evaluation of progression-free survival as a surrogate endpoint for overall survival in locally advanced or metastatic differentiated thyroid cancer: a systematic review

期刊

ENDOCRINE
卷 -, 期 -, 页码 -

出版社

SPRINGER
DOI: 10.1007/s12020-023-03507-3

关键词

Differentiated thyroid cancer; Radioactive iodine refractory; Surrogate endpoint; Progression-free survival; Overall survival

向作者/读者索取更多资源

This study aimed to investigate whether progression-free survival (PFS) could be used as a surrogate endpoint for overall survival (OS) in locally advanced or metastatic differentiated thyroid cancer (DTC) clinical trials. The results showed weak correlation between PFS benefit and OS benefit, and PFS did not meet the statistical criteria for the surrogate endpoint.
PurposePatients with locally advanced or metastatic differentiated thyroid cancer (DTC) have a variable prognosis, and the development of more effective treatment strategies is an important research topic. Overall survival (OS) is the gold standard for research endpoints in randomized controlled trials (RCTs), but observing an OS benefit requires the inclusion of a large number of patients and a long follow-up period. In this study, we aimed to investigate whether progression-free survival (PFS) could be used as a surrogate endpoint for OS in locally advanced or metastatic DTC clinical trials.Materials and methodsWe conducted a search in the PubMed and EMBASE databases to include all RCTs of locally advanced or metastatic DTC and extracted survival data. A weighted linear regression analysis was performed to explore the correlation between PFS benefit and OS benefit by taking the logarithm of the hazard ratios (HRs) of PFS and OS for each trial with a base of 10 and weighted by the number of patients in each RCT.ResultsSeven RCTs, including 1410 patients, were included. At the trial level, PFS benefit was weakly correlated with OS benefit (R2 = 0.210, 95% CI: 0.000-0.811) and did not meet the statistical criteria for the surrogate endpoint.ConclusionThis study does not support PFS as a surrogate endpoint for OS in locally advanced or metastatic DTC clinical trials.Trial registrationPROSPERO Identifier: CRD42022334898

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据