The concomitant use of proton pump inhibitors and BRAF/MEK inhibitors in metastatic melanoma

Author:

Poizeau Florence12ORCID,Balusson Frédéric1ORCID,Lemaitre Florian13,Tron Camille13,Pracht Marc4,Russo David5,Dinulescu Monica5,Lesimple Thierry4ORCID,Oger Emmanuel1ORCID,Dupuy Alain12ORCID

Affiliation:

1. Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, F-35000 Rennes , France

2. Department of Dermatology, Univ Rennes, CHU Rennes , Rennes , France

3. INSERM, Centre d’Investigation Clinique 1414 , F-35000 Rennes , France

4. Department of Medical Oncology, Centre Eugène Marquis , Rennes , France

5. Department of Dermatology , CHU Rennes, Rennes , France

Abstract

Abstract Background Proton-pump inhibitors (PPIs) are commonly used by patients with cancer, although they could reduce the absorption of oral anticancer targeted therapies. The US Food and Drug Administration states that the effect of PPIs on the efficacy of dabrafenib use by patients with metastatic melanoma is unknown. As a precautionary measure, the European Society for Medical Oncology recommends avoiding PPIs for patients receiving dabrafenib. Objectives To determine the effect of the concomitant use of PPIs and BRAF/MEK inhibitors in patients with metastatic melanoma. Methods Patients with advanced melanoma receiving BRAF/MEK inhibitors as first-line treatments between 2015 and 2017 in France were selected using the French National Health Insurance database. We compared time-to-treatment discontinuation (TTD) and overall survival (OS) according to concomitant PPI exposure. We balanced the baseline characteristics of patients exposed and nonexposed to PPIs using an overlap weighting method based on a propensity score. Results The metastatic melanoma cohort comprised 1028 patients receiving BRAF/MEK inhibitors, including 361 (35.1%) patients using PPIs. PPI users had more comorbidities and a more severe metastatic disease. After having equally distributed metastatic sites and comorbidities across patients exposed and nonexposed to PPIs, concomitant PPI use was not associated with shorter TTD [weighted hazard ratio (wHR) 1.03, 95% confidence interval (CI) 0.86–1.24] or OS (wHR 1.11, 95% CI 0.88–1.39). Consistent results were observed when restricting the population to patients receiving dabrafenib, or when narrowing exposure to PPIs with stronger inhibition of cytochromes. Conclusions In a population-based cohort of patients with advanced melanoma, the concomitant use of PPIs and BRAF/MEK inhibitors was not associated with worse outcome.

Funder

Ligue Contre le Cancer

Publisher

Oxford University Press (OUP)

Subject

Dermatology

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