PD-1/PD-L1 inhibitors in endometrial cancer with high microsatellite instability: a Kaplan-Meier-derived patient data meta-analysis.
[INTRODUCTION] Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of solid tumors.
- 95% CI 0.28-0.44
- 연구 설계 meta-analysis
APA
de Moraes FCA, Cavalcanti Souza ME, et al. (2026). PD-1/PD-L1 inhibitors in endometrial cancer with high microsatellite instability: a Kaplan-Meier-derived patient data meta-analysis.. Expert review of anticancer therapy, 26(2), 243-252. https://doi.org/10.1080/14737140.2025.2576617
MLA
de Moraes FCA, et al.. "PD-1/PD-L1 inhibitors in endometrial cancer with high microsatellite instability: a Kaplan-Meier-derived patient data meta-analysis.." Expert review of anticancer therapy, vol. 26, no. 2, 2026, pp. 243-252.
PMID
41093910
Abstract
[INTRODUCTION] Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of solid tumors. This meta-analysis of randomized controlled trials aimed to assess the survival benefit of anti-PD-1/PD-L1 therapies in women with advanced or recurrent endometrial cancer (EC) and mismatch repair deficiency (dMMR).
[METHODS] A systematic search was conducted in PubMed, Scopus, Cochrane, and Web of Science databases to compare PD-1/PD-L1 inhibitors versus standard therapy in patients with advanced/recurrent EC. Studies were screened based on predefined inclusion/exclusion criteria. Risk of bias was assessed using the Cochrane Risk of Bias Tool. We used DerSimonian and Laird random-effects models to estimate hazard ratios (HRs) and risk ratios (RRs) with 95% confidence intervals (CIs).
[RESULTS] Five studies including 2,739 patients were analyzed, with 627 (22.90%) having dMMR tumors. ICIs significantly improved progression-free survival (HR 0.35; 95% CI 0.28-0.44) and overall survival (HR 0.40; 95% CI 0.28-0.57) in dMMR patients. No significant difference was found in objective response rate (RR 1.72; 95% CI 0.88-3.36).
[CONCLUSIONS] The addition of immunotherapy for treating patients with advanced or recurrent endometrial cancer with dMMR and high microsatellite instability significantly improved PFS and OS outcomes.
[REGISTRATION] PROSPERO (CRD22057890200).
[METHODS] A systematic search was conducted in PubMed, Scopus, Cochrane, and Web of Science databases to compare PD-1/PD-L1 inhibitors versus standard therapy in patients with advanced/recurrent EC. Studies were screened based on predefined inclusion/exclusion criteria. Risk of bias was assessed using the Cochrane Risk of Bias Tool. We used DerSimonian and Laird random-effects models to estimate hazard ratios (HRs) and risk ratios (RRs) with 95% confidence intervals (CIs).
[RESULTS] Five studies including 2,739 patients were analyzed, with 627 (22.90%) having dMMR tumors. ICIs significantly improved progression-free survival (HR 0.35; 95% CI 0.28-0.44) and overall survival (HR 0.40; 95% CI 0.28-0.57) in dMMR patients. No significant difference was found in objective response rate (RR 1.72; 95% CI 0.88-3.36).
[CONCLUSIONS] The addition of immunotherapy for treating patients with advanced or recurrent endometrial cancer with dMMR and high microsatellite instability significantly improved PFS and OS outcomes.
[REGISTRATION] PROSPERO (CRD22057890200).
MeSH Terms
Humans; Endometrial Neoplasms; Female; Microsatellite Instability; Immune Checkpoint Inhibitors; Randomized Controlled Trials as Topic; Programmed Cell Death 1 Receptor; DNA Mismatch Repair; Kaplan-Meier Estimate; Neoplasm Recurrence, Local; B7-H1 Antigen; Survival Rate; Progression-Free Survival; Neoplastic Syndromes, Hereditary; Brain Neoplasms; Colorectal Neoplasms
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