Safety of BRAF+MEK Inhibitor Combinations: Severe Adverse Event Evaluation.
Aim: The selective BRAF and MEK inhibitors (BRAFi+MEKi) have substantially improved the survival of melanoma patients with BRAF V600 mutations. However, BRAFi+MEKi can also cause severe or fatal outcomes. We aimed to identify and compare serious adverse events (sAEs) that are significantly associated with BRAFi+MEKi.
Methods: In this pharmacovigilance study, we reviewed FDA Adverse Event Reporting System (FAERS) data in order to detect sAE reporting in patients treated with the combination therapies vemurafenib+cobimetinib (V+C), dabrafenib+trametinib (D+T) and encorafenib+binimetinib (E+B). We evaluated the disproportionate reporting of BRAFi+MEKi-associated sAEs. Significant associations were further analyzed to identify combination-specific safety signals among BRAFi+MEKi.
Results: From January 2018 through June 2019, we identified 11,721 sAE reports in patients receiving BRAFi+MEKi. Comparison of BRAFi+MEKi combinations demonstrates that skin toxicities, including Stevens-Johnson syndrome, were disproportionally reported using V+C, with an age-adjusted reporting odds ratio (adj. ROR) of 3.4 (95%CI, 2.9-4.0), whereas fever was most significantly associated with D+T treatment with an adj. ROR of 1.9 (95%CI, 1.5-2.4). Significant associations using E+B treatment include peripheral neuropathies (adj. ROR 2.7; 95%CI, 1.2-6.1) and renal disorders (adj. ROR 4.1; 95%CI, 1.3-12.5). Notably, we found an increase in the proportion of Guillain-Barre syndrome reports (adj. ROR 8.5; 95%CI, 2.1-35.0) in patients administered E+B.
Conclusion: BRAFi+MEKi combinations share a similar safety profile attributed to class effects, yet concomitantly, these combinations display distinctive effects that can dramatically impact patients' health. Owing to the limitations of pharmacovigilance studies, some findings warrant further validation. However, the possibility of an increased risk for these events should be considered in patient care.
|投稿者||Meirson, Tomer; Asher, Nethanel; Bomze, David; Markel, Gal|
|組織名||Ella Lemelbaum Institute for Immuno-oncology, Sheba Medical Center, Ramat-Gan;526260, Israel.;Azrieli Faculty of Medicine, Bar-Ilan University, Safed 1311502, Israel.;Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.;Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine,;Tel Aviv University, Tel-Aviv 6997801, Israel.|