Prognostic Value of BRAF V600 Mutations in Melanoma Patients After Resection of Metastatic Lymph Nodes |
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Authors: | 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-Fran?ois Emile MD PhD |
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Affiliation: | 1. Department of Pathology, Ambroise Par?? Hospital, Boulogne, France 2. EA4340, Versailles SQY University, Boulogne, France 3. Department of General and Oncologic Dermatology, Ambroise Par?? Hospital, Boulogne, France 4. EA4339, Versailles SQY University, Boulogne, France 5. Public Health Department, Ambroise Par?? Hospital, Boulogne, France 6. EA2506, Versailles SQY University, Boulogne, France 7. Department of Surgery, Ambroise Par?? Hospital, Boulogne, France 8. Department of Radiology, AP-HP, Ambroise Par?? Hospital, Boulogne, France
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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?C3.9) and BRAF status (P?=?0.005, hazard ratio 1.9, 95?% confidence interval 1.2?C3.1). 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. |
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