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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao European Journal of ...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
European Journal of Cancer
Article . 2014 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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BRAF mutation status is an independent prognostic factor for resected stage IIIB and IIIC melanoma: Implications for melanoma staging and adjuvant therapy

Authors: Barbour, Andrew P.; Tang, Yue Hang; Armour, Nicola; Dutton-Regester, Ken; Krause, Lutz; Loffler, Kelly A.; Lambie, Duncan; +4 Authors

BRAF mutation status is an independent prognostic factor for resected stage IIIB and IIIC melanoma: Implications for melanoma staging and adjuvant therapy

Abstract

5-year survival for melanoma metastasis to regional lymph nodes (American Joint Committee on Cancer stage III) is 3cm or extracapsular invasion. Mutations were detected using an extended Sequenom MelaCARTA panel.Mutations were most commonly detected in BRAF (57/124 [46%] patients) and NRAS (26/124 [21%] patients). Patients with BRAF mutations had higher 3-year recurrence rate (77%) versus 54% for BRAF wild-type patients (hazard ratio (HR) 1.8, p=0.008). The only prognostically significant mutations occurred in BRAF: median recurrence-free (RFS) and disease-specific survival (DSS) for BRAF mutation patients was 7 months and 16 months, versus 19 months and not reached for BRAF wild-type patients, respectively. Multivariate analysis identified BRAF mutant status and number of positive lymph nodes as the only independent prognostic factors for RFS and DSS.Patients with BRAF mutations experienced rapid progression of metastatic disease with locoregional recurrence rarely seen in isolation, supporting incorporation of BRAF status into melanoma staging and use of BRAF/MEK inhibitors post-TLND.

Keywords

Male, Proto-Oncogene Proteins B-raf, DNA Mutational Analysis, Kaplan-Meier Estimate, Proto-Oncogene Mas, Outcome Assessment, Health Care, Humans, 1306 Cancer Research, Melanoma, Neoplasm Staging, Proportional Hazards Models, Oncogenes, Middle Aged, Prognosis, Proto-oncogene proteins B-raf, Lymphatic Metastasis, Multivariate Analysis, Mutation, Lymph Node Excision, 2730 Oncology, Female, Immunotherapy, Neoplasm Recurrence, Local, Molecular diagnostic techniques, Follow-Up Studies

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
66
Top 10%
Top 10%
Top 10%
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Cancer Research