Prognostic Value of BRAF V600 Mutations in Melanoma Patients After Resection of Metastatic Lymph Nodes

被引:76
作者
Moreau, Stephanie [1 ,2 ]
Saiag, Philippe [3 ,4 ]
Aegerter, Philippe [5 ,6 ]
Bosset, Daphne [1 ,3 ]
Longvert, Christine [3 ,4 ]
Helias-Rodzewicz, Zofia [1 ,2 ]
Marin, Cristi [1 ,2 ]
Peschaud, Frederique [4 ,7 ]
Chagnon, Sophie [8 ]
Zimmermann, Utte [1 ,4 ]
Clerici, Thierry [1 ,4 ]
Emile, Jean-Francois [1 ,2 ]
机构
[1] Hop Ambroise Pare, Dept Pathol, Boulogne, France
[2] Versailles SQY Univ, EA4340, Boulogne, France
[3] Hop Ambroise Pare, Dept Gen & Oncol Dermatol, Boulogne, France
[4] Versailles SQY Univ, EA4339, Boulogne, France
[5] Hop Ambroise Pare, Dept Publ Hlth, Boulogne, France
[6] Versailles SQY Univ, EA2506, Boulogne, France
[7] Hop Ambroise Pare, Dept Surg, Boulogne, France
[8] Hop Ambroise Pare, AP HP, Dept Radiol, Boulogne, France
关键词
CUTANEOUS MELANOMA; ADJUVANT THERAPY; NRAS MUTATIONS; FEATURES; GENOME; GENE;
D O I
10.1245/s10434-012-2457-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BRAF (V600) mutations are frequent in melanomas, and BRAF(V600)-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 a parts per thousand yen2 mm according to BRAF (V600) mutations and other previously reported prognostic criteria. 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. 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). 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.
引用
收藏
页码:4314 / 4321
页数:8
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