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Thick primary melanoma has a heterogeneous tumor biology: an institutional series

BACKGROUND: Thick melanomas (TM) ≥4 mm have a high risk for nodal and distant metastases. Optimal surgical management, prognostic significance of sentinel node biopsy (SLNB), and benefits of interferon (IFN) for these patients are unclear. As a continuum of increasing tumor thickness is placed into...

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Autores principales: Meguerditchian, Ari-Nareg, Asubonteng, Kobby, Young, Calvin, Lema, Bethany, Wilding, Gregory, Kane III, John M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090362/
https://www.ncbi.nlm.nih.gov/pubmed/21492474
http://dx.doi.org/10.1186/1477-7819-9-40
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author Meguerditchian, Ari-Nareg
Asubonteng, Kobby
Young, Calvin
Lema, Bethany
Wilding, Gregory
Kane III, John M
author_facet Meguerditchian, Ari-Nareg
Asubonteng, Kobby
Young, Calvin
Lema, Bethany
Wilding, Gregory
Kane III, John M
author_sort Meguerditchian, Ari-Nareg
collection PubMed
description BACKGROUND: Thick melanomas (TM) ≥4 mm have a high risk for nodal and distant metastases. Optimal surgical management, prognostic significance of sentinel node biopsy (SLNB), and benefits of interferon (IFN) for these patients are unclear. As a continuum of increasing tumor thickness is placed into a single TM group, differences in biologic and clinical behavior may be lost. The purpose of this study was to better characterize the diverse biology in TM, including the value of increasing thickness and nodal status information, potentially identifying high risk TM subgroups that may warrant more aggressive treatment/follow up. METHODS: 155 consecutive TM patients treated at a single institution between 1971 and 2007 were retrospectively reviewed. Patient, disease and treatment features were analyzed with respect to disease-free (DFS) and overall survival (OS). RESULTS: Median patient age was 66 years and 68% of patients were men. The trunk was the most common TM location (35%), followed by the head and neck (29%) and lower extremities (20%). Median thickness was 6 mm and 61% were ulcerated. 6% patients had stage IV disease, 12% had clinical nodal metastases. Clinically negative lymph node basins were treated by observation (22 patients - 15.4%), elective lymph node dissection (ELND) (24 patients - 17.6%) or SLNB (91 patients - 67%). 75% of ELND's and 53% of SLNB's were positive. Completion node dissection was performed in 38 SLNB+ patients and 22% had additional positive nodes. 17% of the study patients received IFN. At median follow up of 26 months, 5 year DFS and OS were 42% and 43.6%. For SLNB positive vs negative, median DFS were 22 vs 111 months (p = 0.006) and median OS were 41 vs 111 months (p = 0.006). When stratified by tumor thickness ≤ vs > 6 mm, 5 year DFS was 58.3% vs 20% (p < 0.0001) and OS was 62% vs 20% (P < 0.0001). IFN had no impact on DFS or OS (p = 0.98 and 0.8 respectively). CONCLUSION: Within the high risk group of patients with TM, cases with tumor thickness > 6 mm or a positive SLNB had a significantly worse DFS and OS (p < .0001, <.0001 and .006, .006).
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spelling pubmed-30903622011-05-10 Thick primary melanoma has a heterogeneous tumor biology: an institutional series Meguerditchian, Ari-Nareg Asubonteng, Kobby Young, Calvin Lema, Bethany Wilding, Gregory Kane III, John M World J Surg Oncol Research BACKGROUND: Thick melanomas (TM) ≥4 mm have a high risk for nodal and distant metastases. Optimal surgical management, prognostic significance of sentinel node biopsy (SLNB), and benefits of interferon (IFN) for these patients are unclear. As a continuum of increasing tumor thickness is placed into a single TM group, differences in biologic and clinical behavior may be lost. The purpose of this study was to better characterize the diverse biology in TM, including the value of increasing thickness and nodal status information, potentially identifying high risk TM subgroups that may warrant more aggressive treatment/follow up. METHODS: 155 consecutive TM patients treated at a single institution between 1971 and 2007 were retrospectively reviewed. Patient, disease and treatment features were analyzed with respect to disease-free (DFS) and overall survival (OS). RESULTS: Median patient age was 66 years and 68% of patients were men. The trunk was the most common TM location (35%), followed by the head and neck (29%) and lower extremities (20%). Median thickness was 6 mm and 61% were ulcerated. 6% patients had stage IV disease, 12% had clinical nodal metastases. Clinically negative lymph node basins were treated by observation (22 patients - 15.4%), elective lymph node dissection (ELND) (24 patients - 17.6%) or SLNB (91 patients - 67%). 75% of ELND's and 53% of SLNB's were positive. Completion node dissection was performed in 38 SLNB+ patients and 22% had additional positive nodes. 17% of the study patients received IFN. At median follow up of 26 months, 5 year DFS and OS were 42% and 43.6%. For SLNB positive vs negative, median DFS were 22 vs 111 months (p = 0.006) and median OS were 41 vs 111 months (p = 0.006). When stratified by tumor thickness ≤ vs > 6 mm, 5 year DFS was 58.3% vs 20% (p < 0.0001) and OS was 62% vs 20% (P < 0.0001). IFN had no impact on DFS or OS (p = 0.98 and 0.8 respectively). CONCLUSION: Within the high risk group of patients with TM, cases with tumor thickness > 6 mm or a positive SLNB had a significantly worse DFS and OS (p < .0001, <.0001 and .006, .006). BioMed Central 2011-04-14 /pmc/articles/PMC3090362/ /pubmed/21492474 http://dx.doi.org/10.1186/1477-7819-9-40 Text en Copyright ©2011 Meguerditchian et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Meguerditchian, Ari-Nareg
Asubonteng, Kobby
Young, Calvin
Lema, Bethany
Wilding, Gregory
Kane III, John M
Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title_full Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title_fullStr Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title_full_unstemmed Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title_short Thick primary melanoma has a heterogeneous tumor biology: an institutional series
title_sort thick primary melanoma has a heterogeneous tumor biology: an institutional series
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090362/
https://www.ncbi.nlm.nih.gov/pubmed/21492474
http://dx.doi.org/10.1186/1477-7819-9-40
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