AI Article Synopsis

  • Anti-PD-1 antibodies and BRAF/MEK inhibitors can help reduce recurrence risk in resected stage III melanoma patients, and the study investigated the effectiveness of a 'second adjuvant' BRAF/MEKi therapy for those who experienced recurrence after initial treatment.
  • A total of 73 BRAFmut melanoma patients were analyzed, with 61 receiving 'second adjuvant' therapy and showing significant improvements in recurrence-free survival (RFS) compared to those who didn’t receive this treatment.
  • While the second adjuvant therapy led to better RFS, it also resulted in high rates of toxicity, prompting a need for further research on treatment strategies to enhance outcomes while minimizing side effects.

Article Abstract

Background: Anti-PD-1 antibodies and BRAK/MEK inhibitors (BRAF/MEKi) reduce the risk of recurrence for patients with resected stage III melanoma. BRAFV600-mutated (BRAFmut) melanoma patients who recur with isolated disease following adjuvant therapy may be suitable for 'second adjuvant' treatment after local therapy. We sought to examine the efficacy and safety of 'second adjuvant' BRAF/MEKi.

Patients And Methods: Patients with BRAFmut melanoma treated with adjuvant PD-1 based immunotherapy who recurred, underwent definitive local therapy and were then treated with adjuvant BRAF/MEKi were identified retrospectively from 13 centres (second adjuvant group). Demographics, disease and treatment characteristics and outcome data were examined. Outcomes were compared to BRAFmut patients who did not receive 'second adjuvant' therapy (no second adjuvant group).

Results: 73 patients were included; 61 who received 'second adjuvant' therapy and 12 who did not. Most initially recurred on PD-1 therapy (66%). There were no differences in characteristics between groups. 92% of second adjuvant group received dabrafenib and trametinib and median duration of therapy was 11.8 months (0.4, 34.5). 72% required dose adjustments, 23% had grade 3 + toxicity and 38% permanently discontinued drug due to toxicity. After median 26.1 months (1.9, 56.3) follow-up, recurrence-free survival (RFS) was improved in second adjuvant group versus no second adjuvant group (median 30.8 vs 4 months, HR 0.35; p = 0.014), largely driven by a delay in early recurrence, with no difference in overall survival (p = 0.59).

Conclusion: This is the first study examining outcomes of 'second adjuvant' targeted therapy for melanoma, after failure of adjuvant PD-1 based immunotherapy. Data suggest a short-term improvement in RFS, but at the cost of toxicity. Alternative strategies and more data on sequencing adjuvant therapies are required to improve outcomes.

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Source
http://dx.doi.org/10.1016/j.ejca.2024.113561DOI Listing

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