The natural history and patterns of metastases from mucosal melanoma: an analysis of 706 prospectively-followed patients

We examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites. Our hypothesis was that metastatic behavior would differ from primary mucosal melanomas at different anatomical sites. Clinical and pathological data fr...

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Published inAnnals of oncology Vol. 28; no. 4; pp. 868 - 873
Main Authors Lian, B., Cui, C.L., Zhou, L., Song, X., Zhang, X.S., Wu, D., Si, L., Chi, Z.H., Sheng, X.N., Mao, L.L., Wang, X., Tang, B.X., Yan, X.Q., Kong, Y., Dai, J., Li, S.M., Bai, X., Zheng, N., Balch, C.M., Guo, J.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.04.2017
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Abstract We examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites. Our hypothesis was that metastatic behavior would differ from primary mucosal melanomas at different anatomical sites. Clinical and pathological data from 706 patients were compared for their stage distribution, patterns of metastases, CKIT/BRAF mutation status, and overall survival for different anatomical sites. The anatomic sites of the primary mucosal melanomas were from the lower GI tract (26.5%), nasal cavity and paranasal sinuses (23%), gynecological sites (22.5%), oral cavity (15%), urological sites (5%), upper GI tract (5%), and other sites (3.0%). At initial diagnosis, 14.5% were stage I disease, 41% Stage II, 21.5% Stage III, and 23.0% stage IV. Predominant metastatic sites were regional lymph nodes (21.5%), lung (21%), liver (18.5%), and distant nodes (9%). Oral cavity mucosal melanoma had a higher incidence of regional nodal metastases (31.7% versus 19.8%,P = 0.009), and a higher incidence of lung metastases (32.5% versus 18.5%,P = 0.007) compared to other primary mucosal melanomas. There was a 10% incidence of CKIT mutation and 12% BRAF mutation. Mucosal melanomas from nasal pharyngeal and oral, gastrointestinal, gynecological, and urological had a similar survival with a 1-year survival rate (88%, 83%, 86%), 2-year survival rate (66%, 57%, 61%), 5-year survival rate (27%, 16%, 20%), respectively. The largest sample size allows, for the first time, a comparison of primary melanoma stage and patterns of metastases across anatomical sites. With few exceptions, the presenting stages, incidence of nodal and distant metastases, the site of predilection of distant metastases, or overall survival were similar despite different primary anatomic sites. These findings suggest that clinical trials involving mucosal melanomas and the administration of systemic therapy can be applied equally to mucosal melanomas regardless of their primary anatomic site.
AbstractList We examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites. Our hypothesis was that metastatic behavior would differ from primary mucosal melanomas at different anatomical sites. Clinical and pathological data from 706 patients were compared for their stage distribution, patterns of metastases, CKIT/BRAF mutation status, and overall survival for different anatomical sites. The anatomic sites of the primary mucosal melanomas were from the lower GI tract (26.5%), nasal cavity and paranasal sinuses (23%), gynecological sites (22.5%), oral cavity (15%), urological sites (5%), upper GI tract (5%), and other sites (3.0%). At initial diagnosis, 14.5% were stage I disease, 41% Stage II, 21.5% Stage III, and 23.0% stage IV. Predominant metastatic sites were regional lymph nodes (21.5%), lung (21%), liver (18.5%), and distant nodes (9%). Oral cavity mucosal melanoma had a higher incidence of regional nodal metastases (31.7% versus 19.8%, P = 0.009), and a higher incidence of lung metastases (32.5% versus 18.5%, P = 0.007) compared to other primary mucosal melanomas. There was a 10% incidence of CKIT mutation and 12% BRAF mutation. Mucosal melanomas from nasal pharyngeal and oral, gastrointestinal, gynecological, and urological had a similar survival with a 1-year survival rate (88%, 83%, 86%), 2-year survival rate (66%, 57%, 61%), 5-year survival rate (27%, 16%, 20%), respectively. The largest sample size allows, for the first time, a comparison of primary melanoma stage and patterns of metastases across anatomical sites. With few exceptions, the presenting stages, incidence of nodal and distant metastases, the site of predilection of distant metastases, or overall survival were similar despite different primary anatomic sites. These findings suggest that clinical trials involving mucosal melanomas and the administration of systemic therapy can be applied equally to mucosal melanomas regardless of their primary anatomic site.
BackgroundWe examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites. Our hypothesis was that metastatic behavior would differ from primary mucosal melanomas at different anatomical sites. Patients and methodsClinical and pathological data from 706 patients were compared for their stage distribution, patterns of metastases, CKIT/BRAF mutation status, and overall survival for different anatomical sites. ResultsThe anatomic sites of the primary mucosal melanomas were from the lower GI tract (26.5%), nasal cavity and paranasal sinuses (23%), gynecological sites (22.5%), oral cavity (15%), urological sites (5%), upper GI tract (5%), and other sites (3.0%). At initial diagnosis, 14.5% were stage I disease, 41% Stage II, 21.5% Stage III, and 23.0% stage IV. Predominant metastatic sites were regional lymph nodes (21.5%), lung (21%), liver (18.5%), and distant nodes (9%). Oral cavity mucosal melanoma had a higher incidence of regional nodal metastases (31.7% versus 19.8%, P = 0.009), and a higher incidence of lung metastases (32.5% versus 18.5%, P = 0.007) compared to other primary mucosal melanomas. There was a 10% incidence of CKIT mutation and 12% BRAF mutation. Mucosal melanomas from nasal pharyngeal and oral, gastrointestinal, gynecological, and urological had a similar survival with a 1-year survival rate (88%, 83%, 86%), 2-year survival rate (66%, 57%, 61%), 5-year survival rate (27%, 16%, 20%), respectively. ConclusionsThe largest sample size allows, for the first time, a comparison of primary melanoma stage and patterns of metastases across anatomical sites. With few exceptions, the presenting stages, incidence of nodal and distant metastases, the site of predilection of distant metastases, or overall survival were similar despite different primary anatomic sites. These findings suggest that clinical trials involving mucosal melanomas and the administration of systemic therapy can be applied equally to mucosal melanomas regardless of their primary anatomic site.
Author Cui, C.L.
Chi, Z.H.
Mao, L.L.
Wu, D.
Kong, Y.
Yan, X.Q.
Bai, X.
Zhou, L.
Li, S.M.
Guo, J.
Sheng, X.N.
Dai, J.
Balch, C.M.
Si, L.
Song, X.
Zheng, N.
Lian, B.
Wang, X.
Tang, B.X.
Zhang, X.S.
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  organization: Department of Melanoma, Yunnan Cancer Hospital, Kunming
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  organization: Department of Melanoma, SUN YAT-SEN University Cancer Center, Guangzhou
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  organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing
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  organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing
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  organization: Clinical Pharmacology Research Centre, Peking University Cancer Hospital & Institute, Beijing, China
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ContentType Journal Article
Copyright 2016 European Society for Medical Oncology
The Author 2016. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.
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Issue 4
Keywords overall survival
mucosal melanoma
patterns of metastases
natural history
Language English
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McLaughlin (10.1093/annonc/mdw694_bb0060) 2005; 103
Balch (10.1093/annonc/mdw694_bb0070) 1980; 45
Bishop (10.1093/annonc/mdw694_bb0025) 2014; 15
Koivunen (10.1093/annonc/mdw694_bb0055) 2012; 122
Spencer (10.1093/annonc/mdw694_bb0035) 2016; 167
Chang (10.1093/annonc/mdw694_bb0065) 1998; 83
Sun (10.1093/annonc/mdw694_bb0010) 2014; 36
Lian (10.1093/annonc/mdw694_bb0050) 2013; 19
Dauer (10.1093/annonc/mdw694_bb0020) 2008; 138
Lombardi (10.1093/annonc/mdw694_bb0030) 2016; 38
Lyu (10.1093/annonc/mdw694_bb0095) 2016; 45
Marija (10.1093/annonc/mdw694_bb0105) 2012; 5
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Edge (10.1093/annonc/mdw694_bb0045) 2010; 17
Zebary (10.1093/annonc/mdw694_bb0090) 2013; 109
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Snippet We examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites. Our...
BackgroundWe examined whether mucosal melanomas are different in their clinical course and patterns of metastases when arising from different anatomic sites....
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crossref
pubmed
elsevier
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Publisher
StartPage 868
SubjectTerms Adult
Aged
Female
Humans
Male
Melanoma - pathology
Middle Aged
mucosal melanoma
Mucous Membrane - pathology
natural history
Neoplasm Metastasis - pathology
overall survival
patterns of metastases
Title The natural history and patterns of metastases from mucosal melanoma: an analysis of 706 prospectively-followed patients
URI https://dx.doi.org/10.1093/annonc/mdw694
https://www.ncbi.nlm.nih.gov/pubmed/28039178
https://search.proquest.com/docview/1854615254
Volume 28
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