BACKGROUND: Targeted treatment of patients with metastatic BRAF-V600-mutated non-small-cell lung cancer (NSCLC) using BRAF/MEK-inhibitors is effective but limited by acquired resistance. Patients with BRAF-mutant NSCLC may derive long-lasting benefit from immune checkpoint inhibition with PD-1/-L1 antibodies (IO). While IO is the preferred first-line therapy in BRAF-mutated melanoma, the optimal treatment sequence in BRAF-mutated NSCLC is not defined. METHODS: Retrospective study of the clinical outcome of patients with metastatic BRAF-V600-mutated NSCLC diagnosed in the German national Network Genomic Medicine Lung Cancer (nNGM). RESULTS: We identified 205 patients with BRAF-V600-mutated NSCLC. 175 patients received first-line therapy with dabrafenib/trametinib (DAB/TRM, 65.1%), IO alone (19.4%), or chemo-IO (15.4%). Overall survival (OS) and time-to-treatment failure of first-line therapy (TTF) was identical for patients receiving first-line DAB/TRM (median OS 28.0 months) or chemo/IO (27.8 months, HR 1.1, p=0.68). Female patients had superior OS (HR 0.65, p=0.049, confirmed in multivariate model), which was mainly driven by superior OS of female versus male patients receiving first-line DAB/TRM (OS HR 0.53, p=0.015). There was no gender difference in survival of patients receiving IO-based first-line treatment (OS HR 1.02). Surprisingly, high PD-L1 status (TPS
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