Intratumoral regulatory T cells are associated with treatment response to neoadjuvant chemotherapy and prognosis in gastroesophageal adenocarcinoma

Gastroesophageal junction (GEJ) adenocarcinoma is an increasingly common cancer with complex biology and poor prognosis. The treatment strategy for locally advanced tumors involves multimodal treatment with perioperative chemotherapy. However, survival rates remain low, especially for advanced disease. Here, formalin-fixed paraffin-embedded tumor sections from 72 patients with GEJ I and II adenocarcinoma who underwent primary resection or perioperative standard-of-care FLOT treatment were analyzed for their intratumoral T cell composition using multiplex immunohistochemistry. The proportions of T cells and their influence on survival were evaluated using Mann-Whitney <i>U</i> and log rank analyses. A comparison of short- and long-term survivors revealed significant differences in the infiltration of regulatory T cells (Tregs). Tumors after neoadjuvant FLOT treatment presented increased proportions of CD8<sup>+</sup> T cells with reduced Granzyme B expression, indicating an altered immune response. Overall survival analysis revealed that high infiltration of Tregs was associated with poor survival. Notably, responders to FLOT therapy had a greater T cell frequency and improved survival, whereas nonresponders presented higher levels of Tregs and CD8<sup>+</sup> T cells expressing TIM-3. Overall, GEJ cancer patients had increased CD8<sup>+</sup> T cells after neoadjuvant chemotherapy with FLOT, and Tregs were associated with treatment response and reduced survival.

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Publication Details

Journal
OncoImmunology
Published
2025-11-05
DOI
https://doi.org/10.1080/2162402x.2025.2574859
Citations
1
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
1.05
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article

Intratumoral regulatory T cells are associated with treatment response to neoadjuvant chemotherapy and prognosis in gastroesophageal adenocarcinoma

Daniel E. Stange, Heike Polster, Jürgen Weitz, Felix Merboth et al.
1 citations
OncoImmunology
Cancer Immunotherapy and Biomarkers
1.05
article

Intratumoral regulatory T cells are associated with treatment response to neoadjuvant chemotherapy and prognosis in gastroesophageal adenocarcinoma

Daniel E. Stange, Heike Polster, Jürgen Weitz, Felix Merboth, Sascha Brückmann, David Digomann, Loreen Natusch, Franziska Baenke, Lena Seifert, Daniela Ellen Aust, Adrian M. Seifert, Marc Schmitz, Luise Rupp, Antonia Stammberger, Ulrich Sommer
article en
1 citations

Abstract

Gastroesophageal junction (GEJ) adenocarcinoma is an increasingly common cancer with complex biology and poor prognosis. The treatment strategy for locally advanced tumors involves multimodal treatment with perioperative chemotherapy. However, survival rates remain low, especially for advanced disease. Here, formalin-fixed paraffin-embedded tumor sections from 72 patients with GEJ I and II adenocarcinoma who underwent primary resection or perioperative standard-of-care FLOT treatment were analyzed for their intratumoral T cell composition using multiplex immunohistochemistry. The proportions of T cells and their influence on survival were evaluated using Mann-Whitney <i>U</i> and log rank analyses. A comparison of short- and long-term survivors revealed significant differences in the infiltration of regulatory T cells (Tregs). Tumors after neoadjuvant FLOT treatment presented increased proportions of CD8<sup>+</sup> T cells with reduced Granzyme B expression, indicating an altered immune response. Overall survival analysis revealed that high infiltration of Tregs was associated with poor survival. Notably, responders to FLOT therapy had a greater T cell frequency and improved survival, whereas nonresponders presented higher levels of Tregs and CD8<sup>+</sup> T cells expressing TIM-3. Overall, GEJ cancer patients had increased CD8<sup>+</sup> T cells after neoadjuvant chemotherapy with FLOT, and Tregs were associated with treatment response and reduced survival.

OncoImmunologyVol. 14(1)
German Cancer Research Center (DE), Heidelberg University (DE), Helmholtz-Zentrum Dresden-Rossendorf (DE), Institute of Immunology (HR), University Hospital Carl Gustav Carus (DE), Technische Universität Dresden (DE)
Openalex Percentile: Top 16%
Cancer Immunotherapy and Biomarkers
1.05
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