Real-world characterization of PD-L1 expression in patients with advanced esophagogastric adenocarcinoma in Spain

PURPOSE: Epidemiological data from Sapin are lacking, especially in a publication relating Spanish data and prevalence of programmed cell death ligand-1 (PD-L1) expression. This study aimed to evaluate the prevalence of PD-L1 expression by Combined Positive Score (CPS) ≥ 5 in patients with advanced esophagogastric adenocarcinoma (aEGAC) in Spain. METHODS: This observational, retrospective, and multicenter study collected sociodemographic and clinical data from adult patients with locally advanced unresectable, recurrent, or metastatic EGAC across 21 centers in the AGAMENON-SEOM registry. CPS PD-L1 expression was centrally analyzed using the IHC 28-8 pharmDx. RESULTS: A total of 166 patients were included, with 144 valid and evaluable samples. The primary tumor locations were stomach (70.1%), gastroesophageal junction (19.4%), and esophagus (10.4%). At diagnosis, 84.0% had synchronous metastatic disease, 4.9% had unresectable locally advanced disease, and 11.1% had recurrent disease. PD-L1 CPS ≥ 5 was observed in 41.7% of the patients (95%CI, 34.3-50.4%). Prevalence by tumor type was 41.6% (95% CI, 32.0-51.2%) in gastric adenocarcinoma, 35.7% (95% CI, 18.0-53.5%) in gastroesophageal junction adenocarcinomas, and 60.0% (95% CI, 35.2-84.8%) in esophageal adenocarcinoma. PD-L1 CPS ≥ 5 was found in 42.9% (95% CI, 6.2-79.5%) of patients with unresectable locally advanced disease, 43.0% (95% CI, 34.2-51.8%) of those with metastatic disease, and 37.5% (95% CI, 13.8-61.2%) of those with recurrent disease. CONCLUSION: This is the first study to report the real-world prevalence of PD-L1 expression in patients with aEGAC in clinical practice in Spain. These findings underscore the importance of understanding PD-L1 prevalence in the Spanish population and investigating discrepancies with previous studies.

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Journal
Clinical & Translational Oncology
Published
2026-04-28
DOI
https://doi.org/10.1007/s12094-026-04343-3
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
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article

Real-world characterization of PD-L1 expression in patients with advanced esophagogastric adenocarcinoma in Spain

Francisco José Illán-Gambín, Pablo Pérez-Wert, Alberto Carmona‐Bayonas, María Luisa Limón et al.
Clinical & Translational Oncology
Cancer Immunotherapy and Biomarkers
article

Real-world characterization of PD-L1 expression in patients with advanced esophagogastric adenocarcinoma in Spain

Francisco José Illán-Gambín, Pablo Pérez-Wert, Alberto Carmona‐Bayonas, María Luisa Limón, Mireia Gil-Raga, Laura Visa, Paula Jiménez‐Fonseca, Margarita Reboredo, Mar Iglesias‐Coma, Stefania Landolfi, José Luis Domínguez-Miranda, Ana Fernandez-Montes, Rosario Vidal-Tocino, Marta Rodríguez-González, Javier Gallego Plazas, Cinta Hierro, Laura Guerra-Pastrian, María Daniela González, Guillermo Eduardo Mendoza, María Luisa López-Vega, Marc Diez Garcia, Ana Teijo, Juan Luis Catoya-Villa, Eva Martínez de Castro, Andrés Nieto, María Elena Moreno Gutiérrez, David Vilanova
article en

Abstract

PURPOSE: Epidemiological data from Sapin are lacking, especially in a publication relating Spanish data and prevalence of programmed cell death ligand-1 (PD-L1) expression. This study aimed to evaluate the prevalence of PD-L1 expression by Combined Positive Score (CPS) ≥ 5 in patients with advanced esophagogastric adenocarcinoma (aEGAC) in Spain. METHODS: This observational, retrospective, and multicenter study collected sociodemographic and clinical data from adult patients with locally advanced unresectable, recurrent, or metastatic EGAC across 21 centers in the AGAMENON-SEOM registry. CPS PD-L1 expression was centrally analyzed using the IHC 28-8 pharmDx. RESULTS: A total of 166 patients were included, with 144 valid and evaluable samples. The primary tumor locations were stomach (70.1%), gastroesophageal junction (19.4%), and esophagus (10.4%). At diagnosis, 84.0% had synchronous metastatic disease, 4.9% had unresectable locally advanced disease, and 11.1% had recurrent disease. PD-L1 CPS ≥ 5 was observed in 41.7% of the patients (95%CI, 34.3-50.4%). Prevalence by tumor type was 41.6% (95% CI, 32.0-51.2%) in gastric adenocarcinoma, 35.7% (95% CI, 18.0-53.5%) in gastroesophageal junction adenocarcinomas, and 60.0% (95% CI, 35.2-84.8%) in esophageal adenocarcinoma. PD-L1 CPS ≥ 5 was found in 42.9% (95% CI, 6.2-79.5%) of patients with unresectable locally advanced disease, 43.0% (95% CI, 34.2-51.8%) of those with metastatic disease, and 37.5% (95% CI, 13.8-61.2%) of those with recurrent disease. CONCLUSION: This is the first study to report the real-world prevalence of PD-L1 expression in patients with aEGAC in clinical practice in Spain. These findings underscore the importance of understanding PD-L1 prevalence in the Spanish population and investigating discrepancies with previous studies.

Clinical & Translational Oncology
Hospital Universitario La Paz (ES), Hospital General Universitario Morales Meseguer (ES), Complejo Hospitalario de Salamanca (ES), Hospital Universitario 12 De Octubre (ES), Institut Català d'Oncologia (ES), Instituto de Investigación Marqués de Valdecilla (ES), Hospital General Universitario de Elche (ES), Vall d'Hebron Hospital Universitari (ES), Hospital General Universitario De Valencia (ES), Hospital Del Mar (ES), Hospital Universitario Central de Asturias (ES), Instituto de Investigación Biomédica de Salamanca (ES), Badalona Serveis Assistencials (ES), Complexo Hospitalario Universitario A Coruña (ES), Hospital Universitario Virgen del Rocío (ES), Complejo Hospitalario de Ourense (ES)
Bristol-Myers Squibb, Sociedad Española de Oncología Médica, Instituto de Salud Carlos III
Zero hunger
Openalex Percentile: Top 6%
Cancer Immunotherapy and Biomarkers
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