TY - JOUR
T1 - 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
AU - Bührer, Emanuel
AU - Glassee, Nina
AU - Kicinski, Michal
AU - Kennedy, Oliver J.
AU - Blank, Christian U.
AU - Long, Georgina V.
AU - Atkinson, Victoria G.
AU - Dalle, Stéphane
AU - Haydon, Andrew M.
AU - Meshcheryakov, Andrey
AU - Khattak, Adnan
AU - Carlino, Matteo S.
AU - Sandhu, Shahneen
AU - Larkin, James
AU - Puig, Susana
AU - Ascierto, Paolo A.
AU - Rutkowski, Piotr
AU - Schadendorf, Dirk
AU - Boers-Sonderen, Marye
AU - Di Giacomo, Anna Maria
AU - van den Eertwegh, Alfonsus J.M.
AU - Grob, Jean Jacques
AU - Gutzmer, Ralf
AU - Jamal, Rahima
AU - van Akkooi, Alexander C.J.
AU - Gandini, Sara
AU - Valpione, Sara
AU - Suciu, Stefan
AU - Robert, Caroline
AU - Eggermont, Alexander M.M.
AU - Lorigan, Paul
AU - Mandala, Mario
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/1
Y1 - 2025/1
N2 - 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.
AB - 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.
KW - Gastric acid suppressants
KW - Immune-checkpoint inhibitors
KW - Immunotherapy
KW - Pembrolizumab
UR - https://www.scopus.com/pages/publications/105013798947
U2 - 10.1016/j.ejcskn.2025.100727
DO - 10.1016/j.ejcskn.2025.100727
M3 - Article
AN - SCOPUS:105013798947
SN - 2772-6118
VL - 3
JO - EJC Skin Cancer
JF - EJC Skin Cancer
M1 - 100727
ER -