Neoadjuvant pembrolizumab, dabrafenib and trametinib in BRAFV600-mutant resectable melanoma: the randomized phase 2

Georgina V Long1,2,3,4,5, Matteo S Carlino6,7,8,9, George Au-Yeung10,11

  • 1Melanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia. georgina.long@sydney.edu.au.

Nature Medicine
|June 21, 2024
PubMed

Insights

Adding targeted therapy to neoadjuvant immunotherapy for melanoma did not improve long-term outcomes and may reduce response quality. Combining these treatments in the neoadjuvant setting for melanoma is not recommended.

Area of Science:

  • Oncology
  • Immunology
  • Melanoma Research

Background:

  • Immune checkpoint inhibitors and BRAF-targeted therapy are established melanoma treatments.
  • Early immune changes suggest potential synergy between these therapy types.
  • Neoadjuvant immunotherapy aims to improve long-term survival in resectable melanoma.

Purpose of the Study:

  • To evaluate if targeted therapy enhances long-term recurrence-free survival with neoadjuvant immunotherapy.
  • To assess neoadjuvant combination therapy in stage III BRAF-mutant melanoma.
  • To compare pembrolizumab alone versus sequential or concurrent targeted therapy with pembrolizumab.

Main Methods:

  • Phase 2 NeoTrio trial randomized 60 patients with resectable stage III BRAF-mutant melanoma.
  • Treatment arms: pembrolizumab alone, sequential (dabrafenib/trametinib then pembrolizumab), or concurrent (triple) therapy.
  • Outcomes included pathological response, recurrence-free survival, overall survival, and safety.

Main Results:

  • Pathological response rates were 55% (pembrolizumab), 50% (sequential), and 80% (concurrent).
  • Concurrent therapy met the primary outcome, but 2-year event-free survival was 60% (pembrolizumab), 80% (sequential), and 71% (concurrent).
  • Higher recurrence rates observed after major pathological response in targeted therapy arms, suggesting reduced response quality.

Conclusions:

  • Combining targeted therapy with neoadjuvant immunotherapy in melanoma may not improve, and could potentially reduce, response quality.
  • The curative potential of immunotherapy in melanoma should not be risked by combination therapies.
  • Immunotherapy and targeted therapy should not be combined in the neoadjuvant setting for melanoma pending further follow-up.

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