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Subtyping Cutaneous Melanoma Matters
BACKGROUND: Our aim was to investigate the role of melanoma subtype on survival and focus on the effects stratified by Breslow thickness and ulceration status. METHODS: Patients with cutaneous melanoma stage I, II, or III diagnosed between 2000 and 2014 were derived from the Dutch Nationwide Patholo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771426/ https://www.ncbi.nlm.nih.gov/pubmed/33409460 http://dx.doi.org/10.1093/jncics/pkaa097 |
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author | El Sharouni, Mary-Ann van Diest, Paul Johannes Witkamp, Arjen Joost Sigurdsson, Vigfús van Gils, Carla Henrica |
author_facet | El Sharouni, Mary-Ann van Diest, Paul Johannes Witkamp, Arjen Joost Sigurdsson, Vigfús van Gils, Carla Henrica |
author_sort | El Sharouni, Mary-Ann |
collection | PubMed |
description | BACKGROUND: Our aim was to investigate the role of melanoma subtype on survival and focus on the effects stratified by Breslow thickness and ulceration status. METHODS: Patients with cutaneous melanoma stage I, II, or III diagnosed between 2000 and 2014 were derived from the Dutch Nationwide Pathology Registry and overall survival data from the Netherlands Cancer Registry. Patients were followed until 2018. Using multivariable Cox proportional hazards models, hazard ratios were calculated for each melanoma subtype, per Breslow thickness category and ulceration status, and adjusted for age, sex, stage, and localization. RESULTS: A total of 48 361 patients were included: 79.3% had superficial spreading melanoma (SSM), 14.6% nodular melanoma (NM), 5.2% lentigo maligna melanoma, and 0.9% acral lentiginous melanoma (ALM). In the total patient group, using SSM as the reference category, adjusted hazard ratios were 1.06 (95% confidence interval [CI] = 1.01 to 1.12) for NM, 1.02 (95% CI = 0.93 to 1.13) for lentigo maligna melanoma, and 1.26 (95% = CI 1.06 to 1.50) for ALM. Among patients with 1.0 mm or less Breslow thickness and no ulceration, NM showed a twofold increased risk (hazard ratio = 1.96, 95% CI = 1.58 to 2.45) compared with SSM. Compared with 1.0 mm or less SSM without ulceration, the hazard ratio for 1.0 mm or less SSM with ulceration was 1.94 (95% CI = 1.55 to 2.44), and the hazard ratio for 1.0 mm or less NM with ulceration was 3.46 (95% CI = 2.17 to 5.50). NM patients with tumors greater than 1.0 mm did not show worse survival than SSM patients with tumors greater than 1.0 mm. CONCLUSIONS: In this large nationwide study, ALM patients showed worse survival than SSM patients. Among patients with melanomas that were thin (1.0 mm or less), NM subtype patients also showed worse survival than SSM patients. |
format | Online Article Text |
id | pubmed-7771426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77714262021-01-05 Subtyping Cutaneous Melanoma Matters El Sharouni, Mary-Ann van Diest, Paul Johannes Witkamp, Arjen Joost Sigurdsson, Vigfús van Gils, Carla Henrica JNCI Cancer Spectr Article BACKGROUND: Our aim was to investigate the role of melanoma subtype on survival and focus on the effects stratified by Breslow thickness and ulceration status. METHODS: Patients with cutaneous melanoma stage I, II, or III diagnosed between 2000 and 2014 were derived from the Dutch Nationwide Pathology Registry and overall survival data from the Netherlands Cancer Registry. Patients were followed until 2018. Using multivariable Cox proportional hazards models, hazard ratios were calculated for each melanoma subtype, per Breslow thickness category and ulceration status, and adjusted for age, sex, stage, and localization. RESULTS: A total of 48 361 patients were included: 79.3% had superficial spreading melanoma (SSM), 14.6% nodular melanoma (NM), 5.2% lentigo maligna melanoma, and 0.9% acral lentiginous melanoma (ALM). In the total patient group, using SSM as the reference category, adjusted hazard ratios were 1.06 (95% confidence interval [CI] = 1.01 to 1.12) for NM, 1.02 (95% CI = 0.93 to 1.13) for lentigo maligna melanoma, and 1.26 (95% = CI 1.06 to 1.50) for ALM. Among patients with 1.0 mm or less Breslow thickness and no ulceration, NM showed a twofold increased risk (hazard ratio = 1.96, 95% CI = 1.58 to 2.45) compared with SSM. Compared with 1.0 mm or less SSM without ulceration, the hazard ratio for 1.0 mm or less SSM with ulceration was 1.94 (95% CI = 1.55 to 2.44), and the hazard ratio for 1.0 mm or less NM with ulceration was 3.46 (95% CI = 2.17 to 5.50). NM patients with tumors greater than 1.0 mm did not show worse survival than SSM patients with tumors greater than 1.0 mm. CONCLUSIONS: In this large nationwide study, ALM patients showed worse survival than SSM patients. Among patients with melanomas that were thin (1.0 mm or less), NM subtype patients also showed worse survival than SSM patients. Oxford University Press 2020-10-23 /pmc/articles/PMC7771426/ /pubmed/33409460 http://dx.doi.org/10.1093/jncics/pkaa097 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article El Sharouni, Mary-Ann van Diest, Paul Johannes Witkamp, Arjen Joost Sigurdsson, Vigfús van Gils, Carla Henrica Subtyping Cutaneous Melanoma Matters |
title | Subtyping Cutaneous Melanoma Matters |
title_full | Subtyping Cutaneous Melanoma Matters |
title_fullStr | Subtyping Cutaneous Melanoma Matters |
title_full_unstemmed | Subtyping Cutaneous Melanoma Matters |
title_short | Subtyping Cutaneous Melanoma Matters |
title_sort | subtyping cutaneous melanoma matters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771426/ https://www.ncbi.nlm.nih.gov/pubmed/33409460 http://dx.doi.org/10.1093/jncics/pkaa097 |
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