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Adjuvant Treatment of Melanoma
Melanomas represent 4% of all malignant tumors of the skin, yet account for 80% of deaths from skin cancer.While in the early stages patients can be successfully treated with surgical resection, metastatic melanoma prognosis is dismal. Several oncogenes have been identified in melanoma as BRAF, NRAS...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588212/ https://www.ncbi.nlm.nih.gov/pubmed/23476798 http://dx.doi.org/10.1155/2013/545631 |
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author | Moreno Nogueira, J. A. Valero Arbizu, M. Pérez Temprano, R. |
author_facet | Moreno Nogueira, J. A. Valero Arbizu, M. Pérez Temprano, R. |
author_sort | Moreno Nogueira, J. A. |
collection | PubMed |
description | Melanomas represent 4% of all malignant tumors of the skin, yet account for 80% of deaths from skin cancer.While in the early stages patients can be successfully treated with surgical resection, metastatic melanoma prognosis is dismal. Several oncogenes have been identified in melanoma as BRAF, NRAS, c-Kit, and GNA11 GNAQ, each capable of activating MAPK pathway that increases cell proliferation and promotes angiogenesis, although NRAS and c-Kit also activate PI3 kinase pathway, including being more commonly BRAF activated oncogene. The treatment of choice for localised primary cutaneous melanoma is surgery plus lymphadenectomy if regional lymph nodes are involved. The justification for treatment in addition to surgery is based on the poor prognosis for high risk melanomas with a relapse index of 50–80%. Patients included in the high risk group should be assessed for adjuvant treatment with high doses of Interferon-α2b, as it is the only treatment shown to significantly improve disease free and possibly global survival. In the future we will have to analyze all these therapeutic possibilities on specific targets, probably associated with chemotherapy and/or interferon in the adjuvant treatment, if we want to change the natural history of melanomas. |
format | Online Article Text |
id | pubmed-3588212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35882122013-03-09 Adjuvant Treatment of Melanoma Moreno Nogueira, J. A. Valero Arbizu, M. Pérez Temprano, R. ISRN Dermatol Review Article Melanomas represent 4% of all malignant tumors of the skin, yet account for 80% of deaths from skin cancer.While in the early stages patients can be successfully treated with surgical resection, metastatic melanoma prognosis is dismal. Several oncogenes have been identified in melanoma as BRAF, NRAS, c-Kit, and GNA11 GNAQ, each capable of activating MAPK pathway that increases cell proliferation and promotes angiogenesis, although NRAS and c-Kit also activate PI3 kinase pathway, including being more commonly BRAF activated oncogene. The treatment of choice for localised primary cutaneous melanoma is surgery plus lymphadenectomy if regional lymph nodes are involved. The justification for treatment in addition to surgery is based on the poor prognosis for high risk melanomas with a relapse index of 50–80%. Patients included in the high risk group should be assessed for adjuvant treatment with high doses of Interferon-α2b, as it is the only treatment shown to significantly improve disease free and possibly global survival. In the future we will have to analyze all these therapeutic possibilities on specific targets, probably associated with chemotherapy and/or interferon in the adjuvant treatment, if we want to change the natural history of melanomas. Hindawi Publishing Corporation 2013-02-17 /pmc/articles/PMC3588212/ /pubmed/23476798 http://dx.doi.org/10.1155/2013/545631 Text en Copyright © 2013 J. A. Moreno Nogueira et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Moreno Nogueira, J. A. Valero Arbizu, M. Pérez Temprano, R. Adjuvant Treatment of Melanoma |
title | Adjuvant Treatment of Melanoma |
title_full | Adjuvant Treatment of Melanoma |
title_fullStr | Adjuvant Treatment of Melanoma |
title_full_unstemmed | Adjuvant Treatment of Melanoma |
title_short | Adjuvant Treatment of Melanoma |
title_sort | adjuvant treatment of melanoma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588212/ https://www.ncbi.nlm.nih.gov/pubmed/23476798 http://dx.doi.org/10.1155/2013/545631 |
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