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Adjuvant BRAF/MEK versus anti-PD-1 in BRAF-mutant melanoma: a propensity score matched survival analysis.

M Bloem ,
M M de Meza ,
A J M van den Eertwegh ,
M J B Aarts ,
F W P J van den Berkmortel ,
C U Blank ,
W A M Blokx ,
M J Boers-Sonderen ,
J J Bonenkamp ,
C D M Boreel ,
J W B de Groot ,
J B A G Haanen ,
G A P Hospers ,
E Kapiteijn ,
O J van Not ,
D Piersma ,
B Rikhof ,
A M Stevense-den Boer ,
A A M van der Veldt ,
G Vreugdenhil ,
K P M Suijkerbuijk ,
M W J M Wouters

Abstract

METHODS

All stage III BRAF-mutant melanoma patients who received adjuvant BRAF/MEK or anti-PD-1 (2018-2022) were included from the Dutch Melanoma Treatment Registry. Propensity score matching (PSM) was used to compare 1- and 2-year recurrence-free survival (RFS), distant metastasis-free survival (DMFS), and overall survival (OS), and toxicity rates.

CONCLUSION

After PSM, no significant differences in outcomes were observed between adjuvant anti-PD-1 and BRAF/MEK-treated patients with stage III BRAF-mutant melanoma.

BACKGROUND

Adjuvant BRAF/MEK inhibitors (BRAF/MEK) and anti-PD-1 therapy have become the standard care in resected stage III/IV melanoma. A head-to-head clinical trial comparison is lacking.

FINDINGS

Among 952 patients (226 BRAF/MEK and 726 anti-PD-1), BRAF/MEK-treated patients had lower disease stages (16·4% versus 9·9% stage IIIA; p < 0·01) and more often comorbidities (75·2% versus 63·4%; p < 0·01). Median follow-up was 29 months. PSM created two similar groups of 223 patients. RFS, DMFS, and OS were not significantly different before and after PSM. Two-year RFS was 62% (95% CI 55-71) for BRAF/MEK and 65% (95% CI 58-72) for anti-PD-1; 2-year DMFS was 81% (95% CI 74-87) versus 81% (95% CI 75-86); 2-year OS was 86% (95% CI 81-92) versus 89% (95% CI 85-94), respectively. Grade ≥ 3 toxicity was reported in 11·7% (BRAF/MEK) and 13·4% (anti-PD-1).

More about this publication

British journal of cancer

Volume 132
Issue nr. 12
Pages 1124-1130
Publication date 01-06-2025

Full text links

Publisher website (DOI) 10.1038/s41416-025-03021-5
Europe PubMed Central 40234665
Pubmed 40234665

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