ReviewJTO clinical and research reports2026
Prevalence of High Programmed Death-Ligand 1 Expression in Pulmonary Sarcomatoid Carcinoma: A Systematic Review and Meta-Analysis.
Review in JTO clinical and research reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
14 authors.
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Abstract
Pulmonary sarcomatoid carcinoma (PSC) is a rare, aggressive variant of NSCLC associated with emerging evidence of high programmed death-ligand 1 (PD-L1) expression, although its reported prevalence varies widely. We conducted a systematic review and meta-analysis to quantify the pooled prevalence of PD-L1 expression in PSC and identify factors associated with its variability. We searched PubMed, Web of Science, and the Cochrane Library up to November 2025. Studies reporting PD-L1 expression using the tumor proportion score (TPS) in confirmed PSC (≥ 10 patients) were included. A random-effects meta-analysis was performed for TPS thresholds of 50% and 1%. Subgroup analyses and meta-regression were used to explore sources of heterogeneity. This study was registered with PROSPERO (CRD420251243606). Thirty-four studies, encompassing up to 1789 patients, were included. The pooled prevalence of high PD-L1 expression (TPS ≥ 50%) was 57.33%, and PD-L1 positivity (TPS ≥ 1%) was 79.61%. At a TPS of 50% or higher, non-Asian studies reported a numerically higher prevalence than Asian studies, although the difference was not statistically significant. A higher proportion of ever-smokers and a 100% pleomorphic carcinoma composition were each associated with a significantly higher prevalence at a TPS of 1% or higher. In the meta-regression, no covariate reached statistical significance at a TPS of 50% or higher, whereas the proportions of pleomorphic carcinoma, ever-smokers, and median age were significant predictors at a TPS of 1% or higher. PD-L1 expression is remarkably prevalent in PSC, substantially exceeding that in conventional NSCLC. These findings may inform immunotherapy decision-making for advanced PSC.
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