First-line BRAF/MEK inhibitors versus anti-PD-1 monotherapy in BRAF(V600)-mutant advanced melanoma patients: a propensity-matched survival analysis

  • J van Breeschoten
  • , M Wouters
  • , DL Hilarius
  • , JB Haanen
  • , CU Blank
  • , MJB Aarts
  • , F van den Berkmortel
  • , JWB de Groot
  • , GAP Hospers
  • , E Kapiteijn
  • , D Piersma
  • , RS van Rijn
  • , KPM Suijkerbuijk
  • , WAM Blokx
  • , BJJ ten Tije
  • , Astrid van der Veldt
  • , A Vreugdenhil
  • , MJ Boers-Sonderen
  • , AJM Van den Eertwegh

Research output: Contribution to journalArticleAcademicpeer-review

28 Citations (Scopus)
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Abstract

Background: Anti-PD-1 antibodies and BRAF/MEK inhibitors are the two main groups of systemic therapy in the treatment of BRAFV600-mutant advanced melanoma. Until now, data are inconclusive on which therapy to use as first-line treatment. The aim of this study was to use propensity score matching to compare first-line anti-PD-1 monotherapy vs. BRAF/MEK inhibitors in advanced BRAFV600-mutant melanoma patients. Methods: We selected patients diagnosed between 2014 and 2017 with advanced melanoma and a known BRAFV600-mutation treated with first-line BRAF/MEK inhibitors or anti-PD-1 antibodies, registered in the Dutch Melanoma Treatment Registry. Patients were matched based on their propensity scores using the nearest neighbour and the optimal matching method. Results: Between 2014 and 2017, a total of 330 and 254 advanced melanoma patients received BRAF/MEK inhibitors and anti-PD-1 monotherapy as first-line systemic therapy. In the matched cohort, patients receiving anti-PD-1 antibodies as a first-line treatment had a higher median and 2-year overall survival compared to patients treated with first-line BRAF/MEK inhibitors, 42.3 months (95% CI: 37.3-NE) vs. 19.8 months (95% CI: 16.7–24.3) and 65.4% (95% CI: 58.1–73.6) vs. 41.7% (95% CI: 34.2–51.0). Conclusions: Our data suggest that in the matched BRAFV600-mutant advanced melanoma patients, anti-PD-1 monotherapy is the preferred first-line treatment in patients with relatively favourable patient and tumour characteristics.

Original languageEnglish
Pages (from-to)1222-1230
Number of pages9
JournalBritish Journal of Cancer
Volume124
Issue number7
DOIs
Publication statusPublished - 26 Jan 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research programs

  • EMC OR-01

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