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 in | Annals of oncology Vol. 28; no. 4; pp. 868 - 873 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: B. surname: Lian fullname: Lian, B. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 2 givenname: C.L. surname: Cui fullname: Cui, C.L. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 3 givenname: L. surname: Zhou fullname: Zhou, L. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 4 givenname: X. surname: Song fullname: Song, X. organization: Department of Melanoma, Yunnan Cancer Hospital, Kunming – sequence: 5 givenname: X.S. surname: Zhang fullname: Zhang, X.S. organization: Department of Melanoma, SUN YAT-SEN University Cancer Center, Guangzhou – sequence: 6 givenname: D. surname: Wu fullname: Wu, D. organization: Department of Melanoma, The First Hospital of Jilin University, Changchun – sequence: 7 givenname: L. surname: Si fullname: Si, L. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 8 givenname: Z.H. surname: Chi fullname: Chi, Z.H. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 9 givenname: X.N. surname: Sheng fullname: Sheng, X.N. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 10 givenname: L.L. surname: Mao fullname: Mao, L.L. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 11 givenname: X. surname: Wang fullname: Wang, X. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 12 givenname: B.X. surname: Tang fullname: Tang, B.X. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 13 givenname: X.Q. surname: Yan fullname: Yan, X.Q. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 14 givenname: Y. surname: Kong fullname: Kong, Y. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 15 givenname: J. surname: Dai fullname: Dai, J. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 16 givenname: S.M. surname: Li fullname: Li, S.M. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 17 givenname: X. surname: Bai fullname: Bai, X. organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing – sequence: 18 givenname: N. surname: Zheng fullname: Zheng, N. organization: Clinical Pharmacology Research Centre, Peking University Cancer Hospital & Institute, Beijing, China – sequence: 19 givenname: C.M. surname: Balch fullname: Balch, C.M. organization: Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA – sequence: 20 givenname: J. surname: Guo fullname: Guo, J. email: guoj307@126.com organization: Department of Renal Cancer & Melanoma, Peking University Cancer Hospital & Institute, Beijing |
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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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Keywords | overall survival mucosal melanoma patterns of metastases natural history |
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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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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 |
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