Event‐free survival and complete response rate as surrogate endpoints for overall survival in high‐risk non–muscle‐invasive bladder cancer: A meta‐analysis of bacillus Calmette‐Guérin—naive or —remote cases

Read full text
Authors: Rituparna Bhattacharya, Kalé Kponee‐Shovein, Yipeng Gao, Yan Song, Jingyi Liu, Katherine Wei, Ekta Kapadia, Haojie Li, Ashish M. Kamat
Cited by: 1
References: 23

Abstract

Abstract Background Event‐free survival (EFS) and complete response rate (CRR) are recommended as primary endpoints in bladder cancer trials to enable timely assessment of therapeutic benefit. However, their surrogacy relationship with overall survival (OS) in high‐risk non–muscle‐invasive bladder cancer (HR NMIBC) remains unclear. This meta‐analysis evaluated EFS and CRR as surrogate endpoints for OS in bacillus Calmette‐Guérin (BCG)–naive or –remote HR NMIBC. Methods A systematic literature review identified trials enrolling BCG‐naive or ‐remote HR NMIBC patients and reporting EFS, CRR, and OS. Weighted linear regression models estimated trial‐level associations between the hazard ratio (HR) for EFS and HR for OS, odds ratio for CRR and HR for OS, and arm‐level association between median EFS and median OS. Strength of association was quantified using the correlation coefficient ( R ) and coefficient of determination ( R 2 ). Sensitivity analyses evaluated consistency across EFS definitions, publication year, and BCG treatment history. Results Ten eligible trials were identified for surrogacy analyses of EFS and CRR. Strong correlations were observed between EFS and OS at the trial level ( R = 0.85; R 2 = 0.72) and arm level ( R = 0.90; R 2 = 0.82). Trial‐level associations between CRR and OS were weaker ( R 2 = 0.36 for 3‐month CRR; R 2 = 0.30 for 6‐month CRR). Sensitivity analyses confirmed robustness of the primary results. Conclusion In BCG‐naive or ‐remote HR NMIBC, EFS shows strong correlation with OS at the trial and arm levels, supporting its potential as a surrogate endpoint. Further validation incorporating additional trials across varied therapeutic modalities is warranted.

Fields of Study & Subjects

Bladder and Urothelial Cancer Treatments Immune responses and vaccinations Infectious Disease Case Reports and Treatments

Publication details

Journal / source
Cancer
Publisher
Wiley
Volume
132
Issue
3
Pages
e70220–e70220
Publication date
24 January 2026
Language
EN