SynthesisMedicine2026
Beneficial subgroups for PD-1 inhibitor plus chemotherapy in first-line treatment of advanced esophageal squamous cell carcinoma: A systematic review and meta-analysis.
Synthesis in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
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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.
The trial behind it
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Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Overall survival with immune checkpoint inhibitors across treatment settings and clinical and PD-L1-defined subgroups in advanced esophageal squamous cell carcinoma: a systematic review and meta-analysis of randomized trials.Frontiers in immunology · 2026Pooled it
- PVR Mediates Resistance to IL21.CD276.CAR-T Therapy in Esophageal Squamous Cell Carcinoma.International journal of molecular sciences · 2026Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundEsophageal cancer exhibits peak incidence in Asia and Africa, representing the sixth most common malignancy and seventh leading cause of global cancer mortality. Esophageal squamous cell carcinoma (ESCC) constitutes 90% of esophageal cancer cases. The European Medicines Agency approved programmed death 1 (PD-1) inhibitors plus chemotherapy as a first-line treatment for high PD-1-expressing ESCC.
methodsWe systematically searched randomized controlled trials of PD-1 or PD-L1 inhibitors as first-line treatment from PubMed, Embase, and Cochrane Library. The following outcomes were combined: overall survival, progression-free survival, objective response rate, and treatment-related adverse events (TRAEs). Bias risk was rigorously evaluated using the Cochrane Risk of Bias Tool. RevMan 5.3 and R Studio (Boston) were utilized for data synthesis in this meta-analysis, with sensitivity analyses comparing fixed- and random-effects models to reinforce findings.
resultsA total of 4702 patients (PD-1 inhibitors plus chemotherapy: 2529; chemotherapy: 2173) were enrolled in 8 randomized controlled trials. Compared with conventional chemotherapy, first-line PD-1 inhibitors plus chemotherapy significantly improved the overall survival (hazard ratio = 0.68, 95% confidence interval (CI): 0.63-0.74; P < .00001) and objective response rate (relative risk [RR] = 2.03, 95% CI: 1.80-2.29; P < .00001) of advanced ESCC patients. Moreover, PD-1 inhibitor-based therapy provided benefits in progression-free survival (hazard ratio = 0.62, 95% CI: 0.58-0.66; P < .00001). But PD-1 inhibitors were not associated with statistically lower incidences of TRAEs and grade 3 to 5 TRAEs. In subgroup analyses, except the limited benefit observed in the programmed death-ligand 1 (PD-L1) combined positive score < 1 subgroup, none of the following factors significantly influenced the efficacy of PD-1 inhibitor therapy: advanced age, metastatic status, number of metastatic organs, or presence of liver metastases.
conclusionThe combination of PD-1 inhibitors with chemotherapy demonstrates superior efficacy as first-line therapy for advanced esophageal squamous cell carcinoma. Both elderly patients and those with metastatic involvement derive universal benefit without increased adverse risks. However, patients with PD-L1 combined positive score < 1 may experience restricted clinical benefits. Thus, more precise predictive markers are required to stratify potential responders, enabling broader patient populations to derive benefits from PD-1 inhibitor-chemotherapy regimens.
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