Prognostic and predictive value of gastric acid suppressants in the EORTC 1325/KEYNOTE-054 randomized phase III trial of pembrolizumab vs placebo in resected stage III melanoma

Background: The gut microbiome plays a pivotal role in regulating immunity. Gastric acid suppressants (GAS) are known to alter the gut microbiome and might therefore modify response to immunotherapy in cancer patients. We estimated associations of GAS with recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) in the EORTC 1325/KEYNOTE-054 trial. Methods: Patients with resected stage III melanoma were randomized to receive 200 mg of pembrolizumab or placebo. Pembrolizumab prolonged RFS and DMFS (reported elsewhere). We used Cox models to estimate hazard ratios (HR) and 95 % confidence intervals (CI) for the association between GAS at baseline, and RFS and DMFS, overall and by treatment arm. Results: Out of 1019 randomized patients, 109 (10.7 %) used GAS at baseline. We did not find a prognostic importance for RFS (HR 1.06, 95 % CI 0.79–1.42) or DMFS (HR 1.05, 95 % CI 0.77–1.43), neither a predictive importance (HR for RFS in the pembrolizumab arm: 1.02 (95 % CI 0.66–1.56) and 1.09 (95 % CI 0.74–1.62) in the placebo arm (p = 0.81); corresponding HRs for DMFS: 1.17 (95 % CI 0.75–1.82) and 0.95 (95 % CI 0.62–1.48) (p = 0.52)). Conclusion: GAS showed no impact on RFS or DMFS in patients with stage III melanoma receiving adjuvant pembrolizumab or placebo.

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Publication Details

Journal
EJC Skin Cancer
Published
2025-01-01
DOI
https://doi.org/10.1016/j.ejcskn.2025.100727
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
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article

Prognostic and predictive value of gastric acid suppressants in the EORTC 1325/KEYNOTE-054 randomized phase III trial of pembrolizumab vs placebo in resected stage III melanoma

Mario Mandalà, Sara Gandini, Ralf Gutzmer, Sara Valpione et al.
EJC Skin Cancer
Cancer Immunotherapy and Biomarkers
article

Prognostic and predictive value of gastric acid suppressants in the EORTC 1325/KEYNOTE-054 randomized phase III trial of pembrolizumab vs placebo in resected stage III melanoma

Mario Mandalà, Sara Gandini, Ralf Gutzmer, Sara Valpione, Paolo A. Ascierto, Emanuel Buehrer, Michal Kiciński, Dirk Schadendorf, Andrey Meshcheryakov, Nina Glassée, Stefan Suciu, Oliver John Kennedy, Jean‐Jacques Grob, Shahneen Kaur Sandhu, Paul C. Lorigan, Georgina Venetia Long, Alfons J.M. van den Eertwegh, Stéphane Dalle, Piotr Rutkowski, Alexander C. J. van Akkooi, James Larkin, Susana Puig, Matteo Salvatore Carlino, Christian U. Blank, Andrew Haydon, Caroline Robert, Rahima Jamal, Victoria Atkinson, Anna Maria Di Giacomo, Marye J. Boers‐Sonderen, Alexander M.M. Eggermont, Adnan Khattak
article en

Abstract

Background: The gut microbiome plays a pivotal role in regulating immunity. Gastric acid suppressants (GAS) are known to alter the gut microbiome and might therefore modify response to immunotherapy in cancer patients. We estimated associations of GAS with recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) in the EORTC 1325/KEYNOTE-054 trial. Methods: Patients with resected stage III melanoma were randomized to receive 200 mg of pembrolizumab or placebo. Pembrolizumab prolonged RFS and DMFS (reported elsewhere). We used Cox models to estimate hazard ratios (HR) and 95 % confidence intervals (CI) for the association between GAS at baseline, and RFS and DMFS, overall and by treatment arm. Results: Out of 1019 randomized patients, 109 (10.7 %) used GAS at baseline. We did not find a prognostic importance for RFS (HR 1.06, 95 % CI 0.79–1.42) or DMFS (HR 1.05, 95 % CI 0.77–1.43), neither a predictive importance (HR for RFS in the pembrolizumab arm: 1.02 (95 % CI 0.66–1.56) and 1.09 (95 % CI 0.74–1.62) in the placebo arm (p = 0.81); corresponding HRs for DMFS: 1.17 (95 % CI 0.75–1.82) and 0.95 (95 % CI 0.62–1.48) (p = 0.52)). Conclusion: GAS showed no impact on RFS or DMFS in patients with stage III melanoma receiving adjuvant pembrolizumab or placebo.

EJC Skin CancerVol. 3
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Hexal AG, Array BioPharma, Regeneron Pharmaceuticals, Les Laboratories Pierre Fabre, Innovent Biologics, SkylineDx, Moderna, Eisai, Sun Pharma, Italfarmaco, Qbiotics, LEO Pharma, Genentech
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Cancer Immunotherapy and Biomarkers
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