P17.15.A ASSOCIATION OF PROTON PUMP INHIBITOR USE WITH OUTCOME OF PATIENTS WITH NEWLY DIAGNOSED GLIOBLASTOMA

Abstract BACKGROUND Proton pump inhibitors (PPI) are often prescribed to prevent steroid-induced gastritis and peptic ulcer disease in patients with glioblastoma. Yet, these drugs may enhance the activity of aldehyde dehydrogenase 1 A1 (ALDH1A1) which has been linked to protection from oxidative stress, radiotherapy and chemotherapy. MATERIAL AND METHODS We analyzed data from 2981 patients enrolled into 5 randomized clinical trials for newly diagnosed glioblastoma to explore an association of the use of potent ALDH1A1-activating PPI (PA-PPI) and other anti-acid drugs with outcome. We assessed drug use at baseline and at defined landmarks: start of temozolomide maintenance cycles 1 (landmark 1) and 4 (landmark 2), and end of cycle 6 (landmark 3). RESULTS On univariate analysis, we noted inferior progression-free and overall survival for patients treated with PA-PPI at all 4 time points. The multivariate analysis accounting for age, sex, performance status, steroid use, extent of resection, and O6-methylguanine DNA methyltransferase promoter methylation (MGMT) status confirmed a difference for progression-free survival at landmarks 1, 2 and 3, and for overall survival at landmarks 1 and 2. No such effect was seen for the use of other anti-acid drugs. The negative association of PA-PPI use with outcome was observed independently of MGMT promoter methylation and of steroid use. CONCLUSION We conclude that PA-PPI use should be discouraged in patients with glioblastoma since alternative agents are available and since a detrimental effect cannot be excluded. Translational research studies should explore whether PPI-induced activity of ALDH mediates the potential adverse effects of PPI in glioblastoma.

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Journal
Neuro-Oncology
Published
2025-10-01
DOI
https://doi.org/10.1093/neuonc/noaf193.531
Primary Topic
ATP Synthase and ATPases Research
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article
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article

P17.15.A ASSOCIATION OF PROTON PUMP INHIBITOR USE WITH OUTCOME OF PATIENTS WITH NEWLY DIAGNOSED GLIOBLASTOMA

Warren Mason, Jaap C. Reijneveld, Michael Weller, Debaleena Sain et al.
Neuro-Oncology
ATP Synthase and ATPases Research
article

P17.15.A ASSOCIATION OF PROTON PUMP INHIBITOR USE WITH OUTCOME OF PATIENTS WITH NEWLY DIAGNOSED GLIOBLASTOMA

Warren Mason, Jaap C. Reijneveld, Michael Weller, Debaleena Sain, Thierry Gorlia, Julian R. Sampson, Patrick Roth, Roger Stupp, Matthias Preusser, David A. Reardon, Timothy F. Cloughesy, Burt Nabors, Émilie Le Rhun, Wolfgang Wick, Giuseppe Caracciolo Minniti, E. Sara
article en

Abstract

Abstract BACKGROUND Proton pump inhibitors (PPI) are often prescribed to prevent steroid-induced gastritis and peptic ulcer disease in patients with glioblastoma. Yet, these drugs may enhance the activity of aldehyde dehydrogenase 1 A1 (ALDH1A1) which has been linked to protection from oxidative stress, radiotherapy and chemotherapy. MATERIAL AND METHODS We analyzed data from 2981 patients enrolled into 5 randomized clinical trials for newly diagnosed glioblastoma to explore an association of the use of potent ALDH1A1-activating PPI (PA-PPI) and other anti-acid drugs with outcome. We assessed drug use at baseline and at defined landmarks: start of temozolomide maintenance cycles 1 (landmark 1) and 4 (landmark 2), and end of cycle 6 (landmark 3). RESULTS On univariate analysis, we noted inferior progression-free and overall survival for patients treated with PA-PPI at all 4 time points. The multivariate analysis accounting for age, sex, performance status, steroid use, extent of resection, and O6-methylguanine DNA methyltransferase promoter methylation (MGMT) status confirmed a difference for progression-free survival at landmarks 1, 2 and 3, and for overall survival at landmarks 1 and 2. No such effect was seen for the use of other anti-acid drugs. The negative association of PA-PPI use with outcome was observed independently of MGMT promoter methylation and of steroid use. CONCLUSION We conclude that PA-PPI use should be discouraged in patients with glioblastoma since alternative agents are available and since a detrimental effect cannot be excluded. Translational research studies should explore whether PPI-induced activity of ALDH mediates the potential adverse effects of PPI in glioblastoma.

Neuro-OncologyVol. 27(Supplement_3)
University of Toronto (CA), Heidelberg University (DE), UCLA Health (US), Edinburgh Cancer Research (GB), Princess Margaret Cancer Centre (CA), University of Alabama at Birmingham (US), University Hospital of Zurich (CH), Center for Neuro-Oncology (US), European Organisation for Research and Treatment of Cancer (BE), Amsterdam University Medical Centers (NL), Pediatric Brain Tumor Foundation (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Medical University of Vienna (AT), Heidelberg University (US), Sapienza University of Rome (IT), University of Amsterdam (NL)
Openalex Percentile: Top 76%
ATP Synthase and ATPases Research
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