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Efficacy and safety of dabrafenib–trametinib in the treatment of unresectable advanced/metastatic melanoma with BRAF-V600 mutation: A systematic review and network meta-analysis

  • Nathaly Garzón-Orjuela
  • , Laura Prieto-Pinto
  • , Pieralessandro Lasalvia
  • , Daniel Herrera
  • , Johanna Castrillón
  • , Diana González-Bravo
  • , Camilo Castañeda-Cardona
  • , Diego Rosselli

Research output: Contribution to journalReview articlepeer-review

19 Scopus citations

Abstract

The current systematic review aimed to evaluate and compare the efficacy and safety of dabrafenib–trametinib with those of other therapeutic alternatives in the treatment of patients with unresectable advanced/metastatic melanoma with BRAF-V600 mutation. The search was carried out on four databases up to July 2018. Two separate network meta-analyses (NMA) were performed using the frequentist method (random effects): one with an exclusive population with BRAF-V600 mutation (NMA-pBRAFV600) and another with mixed population (with or without the mutation: NMA-pMixed). An evidence profile was included using the GRADE method for NMA. The validity of the final estimator in the NMA-pMixed was assessed via a sensitivity analysis. Nine clinical trials were included in the NMA-pBRAFV600. Dabrafenib–trametinib was found to have a favorable effect on overall survival (OS) and progression-free survival (PFS) compared with dabrafenib, vemurafenib, and dacarbazine and on partial response rate (PRR) and overall response rate compared with dacarbazine and vemurafenib. In the NMA-pMixed, dabrafenib–trametinib was found to have a positive effect on OS versus ipilimumab 3 mg/kg and on PFS and PRR versus ipilimumab, nivolumab, and pembrolizumab. However, dabrafenib–trametinib and vemurafenib–cobimetinib significantly differed in terms of efficacy. In addition, dabrafenib–trametinib has a favorable effect on Grades 3 and 4 adverse events.

Original languageEnglish
Article numbere13145
JournalDermatologic Therapy
Volume33
Issue number2
DOIs
StatePublished - 01 Mar 2020

Keywords

  • antineoplastics agents
  • melanoma
  • network meta-analysis
  • progression-free survival
  • survival

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