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A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()()
Melanoma incidence and mortality are on the rise and although most new cases of melanoma are thin, a significant percentage of these patients still experience disease progression. The American Joint Committee on Cancer publishes staging criteria for melanoma, which were recently updated to the 8(th)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116825/ https://www.ncbi.nlm.nih.gov/pubmed/30175212 http://dx.doi.org/10.1016/j.ijwd.2018.01.003 |
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author | Chiaravalloti, A.J. Jinna, S. Kerr, P.E. Whalen, J. Grant-Kels, J.M. |
author_facet | Chiaravalloti, A.J. Jinna, S. Kerr, P.E. Whalen, J. Grant-Kels, J.M. |
author_sort | Chiaravalloti, A.J. |
collection | PubMed |
description | Melanoma incidence and mortality are on the rise and although most new cases of melanoma are thin, a significant percentage of these patients still experience disease progression. The American Joint Committee on Cancer publishes staging criteria for melanoma, which were recently updated to the 8(th) edition. The most significant revision from the 7(th) edition affects the T1b classification, which now includes melanomas with a Breslow depth of 0.8 mm to 1.0 mm. The second major revision eliminates mitoses as a criterion to upstage a thin melanoma to T1b. Although mitotic figures have been established as an independent prognostic factor, they do not have a significant correlation with sentinel lymph node (SLN) biopsy positivity. SLN status remains the most important independent prognostic factor in thin melanomas. Nonetheless, the identification of patients who are at the highest risk for having a positive SLN test result remains difficult. Importantly, a positive SLN test result has high positive predictive value, but a negative one has very low negative predictive value. Since there is no proven survival benefit in performing an SLN biopsy in T1 disease, dermatologists need to have a personalized discussion with patients with thin melanomas to review expected risks and benefits before undertaking this procedure. |
format | Online Article Text |
id | pubmed-6116825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61168252018-08-31 A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() Chiaravalloti, A.J. Jinna, S. Kerr, P.E. Whalen, J. Grant-Kels, J.M. Int J Womens Dermatol Article Melanoma incidence and mortality are on the rise and although most new cases of melanoma are thin, a significant percentage of these patients still experience disease progression. The American Joint Committee on Cancer publishes staging criteria for melanoma, which were recently updated to the 8(th) edition. The most significant revision from the 7(th) edition affects the T1b classification, which now includes melanomas with a Breslow depth of 0.8 mm to 1.0 mm. The second major revision eliminates mitoses as a criterion to upstage a thin melanoma to T1b. Although mitotic figures have been established as an independent prognostic factor, they do not have a significant correlation with sentinel lymph node (SLN) biopsy positivity. SLN status remains the most important independent prognostic factor in thin melanomas. Nonetheless, the identification of patients who are at the highest risk for having a positive SLN test result remains difficult. Importantly, a positive SLN test result has high positive predictive value, but a negative one has very low negative predictive value. Since there is no proven survival benefit in performing an SLN biopsy in T1 disease, dermatologists need to have a personalized discussion with patients with thin melanomas to review expected risks and benefits before undertaking this procedure. Elsevier 2018-06-11 /pmc/articles/PMC6116825/ /pubmed/30175212 http://dx.doi.org/10.1016/j.ijwd.2018.01.003 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Chiaravalloti, A.J. Jinna, S. Kerr, P.E. Whalen, J. Grant-Kels, J.M. A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title | A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title_full | A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title_fullStr | A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title_full_unstemmed | A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title_short | A deep look into thin melanomas: What’s new for the clinician and the impact on the patient()() |
title_sort | deep look into thin melanomas: what’s new for the clinician and the impact on the patient()() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116825/ https://www.ncbi.nlm.nih.gov/pubmed/30175212 http://dx.doi.org/10.1016/j.ijwd.2018.01.003 |
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