Erschienen in:
01.12.2012 | Melanomas
Prognostic Value of BRAF
V600 Mutations in Melanoma Patients After Resection of Metastatic Lymph Nodes
verfasst von:
Stéphanie Moreau, MD, Philippe Saiag, MD, PhD, Philippe Aegerter, MD, PhD, Daphné Bosset, MD, Christine Longvert, MD, Zofia Hélias-Rodzewicz, PhD, Cristi Marin, MD, Frédérique Peschaud, MD, PhD, Sophie Chagnon, MD, PhD, Utte Zimmermann, MD, Thierry Clerici, MD, Jean-François Emile, MD, PhD
Erschienen in:
Annals of Surgical Oncology
|
Ausgabe 13/2012
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Abstract
Purpose
BRAF
V600 mutations are frequent in melanomas, and BRAFV600-targeted therapy have dramatic, but often transitory, efficacy in stage IV patients. Prognosis of patients with American Joint Committee on Cancer (AJCC) stage III melanoma is heterogeneous. We aimed to determine the overall survival (OS) of stage III patients with a nodal deposit of ≥2 mm according to BRAF
V600 mutations and other previously reported prognostic criteria.
Methods
This retrospective study included 105 consecutive patients with stage III cutaneous melanomas. Most patients underwent a prospective follow-up. BRAF
V600 mutations were detected by sequencing and pyrosequencing of DNA in samples containing >60 % melanoma cells.
Results
BRAF mutations (p.V600E and p.V600K in 83 and 14 % of cases, respectively) were detected in 40 % of the patients. For patients with and without BRAF mutations, death occurred in 83.3 and 60.3 %, with a median OS of 1.4 and 2.8 years, respectively. Patient age, primary melanoma ulceration, number of invaded lymph nodes, AJCC staging at study entry, and BRAF status were linked to OS in the univariate analysis. The only characteristics associated with OS in the multivariate analysis were number of invaded lymph nodes (P = 0.005, hazard ratio 2.2, 95 % confidence interval 1.3–3.9) and BRAF status (P = 0.005, hazard ratio 1.9, 95 % confidence interval 1.2–3.1).
Conclusions
BRAF
V600 status could be used to stage melanoma patients with nodal deposits. Our results may also help to plan adjuvant trials in these patients, for whom the low tumor load may induce longer efficacy of BRAF-targeted therapies.