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Clinical significance of BRAF mutations in metastatic melanoma

Forty to eighty percent of melanoma tumors have activating mutations in BRAF although the clinical importance of these mutations is not clear. We previously reported an analysis of BRAF mutations in metastatic melanoma samples from 68 patients. In this study, we correlated patient baseline character...

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Autores principales: Chang, David Z, Panageas, Katherine S, Osman, Iman, Polsky, David, Busam, Klaus, Chapman, Paul B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544849/
https://www.ncbi.nlm.nih.gov/pubmed/15613230
http://dx.doi.org/10.1186/1479-5876-2-46
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author Chang, David Z
Panageas, Katherine S
Osman, Iman
Polsky, David
Busam, Klaus
Chapman, Paul B
author_facet Chang, David Z
Panageas, Katherine S
Osman, Iman
Polsky, David
Busam, Klaus
Chapman, Paul B
author_sort Chang, David Z
collection PubMed
description Forty to eighty percent of melanoma tumors have activating mutations in BRAF although the clinical importance of these mutations is not clear. We previously reported an analysis of BRAF mutations in metastatic melanoma samples from 68 patients. In this study, we correlated patient baseline characteristics, prognostic factors, and/or clinical outcomes with the presence of BRAF mutations. No significant differences were observed in age, gender, location of primary melanoma, stage at the diagnosis, and depth of primary tumor between patients with and without BRAF mutations. Melanomas harboring BRAF mutations were more likely to metastasize to liver (P = 0.02) and to metastasize to multiple organs (P = 0.048). Neither time to progression to stage IV nor overall survival were associated with BRAF mutations. In conclusion, we observed no significant differences in clinical characteristics or outcomes between melanomas with or without BRAF mutations. Although there was an increased frequency of liver metastasis and tendency to metastasize to multiple organs in tumors with BRAF mutations, there was no detectable effect on survival. Future prospective studies should include analysis of whether BRAF mutations in melanoma tumors correlate with an increased tendency to metastasize to liver or to multiple organs.
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spelling pubmed-5448492005-01-21 Clinical significance of BRAF mutations in metastatic melanoma Chang, David Z Panageas, Katherine S Osman, Iman Polsky, David Busam, Klaus Chapman, Paul B J Transl Med Research Forty to eighty percent of melanoma tumors have activating mutations in BRAF although the clinical importance of these mutations is not clear. We previously reported an analysis of BRAF mutations in metastatic melanoma samples from 68 patients. In this study, we correlated patient baseline characteristics, prognostic factors, and/or clinical outcomes with the presence of BRAF mutations. No significant differences were observed in age, gender, location of primary melanoma, stage at the diagnosis, and depth of primary tumor between patients with and without BRAF mutations. Melanomas harboring BRAF mutations were more likely to metastasize to liver (P = 0.02) and to metastasize to multiple organs (P = 0.048). Neither time to progression to stage IV nor overall survival were associated with BRAF mutations. In conclusion, we observed no significant differences in clinical characteristics or outcomes between melanomas with or without BRAF mutations. Although there was an increased frequency of liver metastasis and tendency to metastasize to multiple organs in tumors with BRAF mutations, there was no detectable effect on survival. Future prospective studies should include analysis of whether BRAF mutations in melanoma tumors correlate with an increased tendency to metastasize to liver or to multiple organs. BioMed Central 2004-12-21 /pmc/articles/PMC544849/ /pubmed/15613230 http://dx.doi.org/10.1186/1479-5876-2-46 Text en Copyright © 2004 Chang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chang, David Z
Panageas, Katherine S
Osman, Iman
Polsky, David
Busam, Klaus
Chapman, Paul B
Clinical significance of BRAF mutations in metastatic melanoma
title Clinical significance of BRAF mutations in metastatic melanoma
title_full Clinical significance of BRAF mutations in metastatic melanoma
title_fullStr Clinical significance of BRAF mutations in metastatic melanoma
title_full_unstemmed Clinical significance of BRAF mutations in metastatic melanoma
title_short Clinical significance of BRAF mutations in metastatic melanoma
title_sort clinical significance of braf mutations in metastatic melanoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC544849/
https://www.ncbi.nlm.nih.gov/pubmed/15613230
http://dx.doi.org/10.1186/1479-5876-2-46
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