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Clinical Outcomes With Dabrafenib Plus Trametinib in a Clinical Trial Versus Real-World Standard of Care in Patients With BRAF-Mutated Advanced NSCLC

Bruce E. Johnson, Christina S. Baik, Julien Mazières, Harry J.M. Groen, Barbara Melosky, Jürgen Wolf, Fatemeh Asad Zadeh Vosta Kolaei, Wen-Hsing Wu, Stefanie Knoll, Meryem Ktiouet Dawson, Adam Johns, David Planchard

2022JTO Clinical and Research Reports20 citationsDOIOpen Access PDF

Abstract

Introduction: -mutated aNSCLC. Methods: -mutated aNSCLC receiving first-line platinum-based chemotherapy (PBC), first-line immune checkpoint inhibitors (ICIs) plus PBC, or second-line ICIs. Weighting by odds was used to estimate the average treatment effect of the treated. Results: = 0.03), respectively; unweighted and weighted median overall survival was 17.3 (12.3-40.2) versus 14.5 (9.2-19.6) months and 17.3 (14.6-not reached) versus 9.7 (6.4-19.6) months, respectively. Hazard ratio of death in unweighted and weighted analyses was 0.56 (0.29-1.1) and 0.57 (0.28-1.17), respectively, with first-line dab-tram versus PBC plus ICI, and 0.65 (0.39-1.07) and not reported (Cox proportional-hazards assumption violated), respectively, with second-line dab-tram versus ICI. Conclusions: -mutated aNSCLC, the risk of death was lower and median overall survival was longer with first-line dab-tram versus PBC. In analyses of dab-tram versus first-line PBC plus ICI or second-line ICI, sample sizes were small and findings were inconclusive with overlapping confidence intervals. Despite some limitations, the study provides useful data for this rare patient population.

Topics & Concepts

DabrafenibHazard ratioMedicineTrametinibInternal medicineOncologyConfidence intervalProportional hazards modelVemurafenibCancerMetastatic melanomaKinaseBiologyMAPK/ERK pathwayCell biologyMelanoma and MAPK PathwaysLung Cancer Treatments and MutationsCancer Immunotherapy and Biomarkers