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Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma

BACKGROUND: In staging patients with clinical stage I-II melanoma, the sentinel lymph node (SLN) is the most important prognostic indicator; however, the false negative rate of SLN biopsy (SLNB) is 15%. METHODS: Nine patients with clinical Stage I-II melanoma underwent SLNB with repeated intraoperat...

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Autores principales: Holder, Ashley M., Ziemys, Arturas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518046/
https://www.ncbi.nlm.nih.gov/pubmed/33042804
http://dx.doi.org/10.3389/fonc.2020.01607
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author Holder, Ashley M.
Ziemys, Arturas
author_facet Holder, Ashley M.
Ziemys, Arturas
author_sort Holder, Ashley M.
collection PubMed
description BACKGROUND: In staging patients with clinical stage I-II melanoma, the sentinel lymph node (SLN) is the most important prognostic indicator; however, the false negative rate of SLN biopsy (SLNB) is 15%. METHODS: Nine patients with clinical Stage I-II melanoma underwent SLNB with repeated intraoperative radiotracer measurements to determine lymphatic transport efficiency (LTE), which was correlated with clinicopathologic data. RESULTS: LTE demonstrated the potential to predict SLN status. LTE in patients with occult nodal metastasis is 40 times faster than those with negative SLNBs. There was no confounding of LTE by clinicopathologic factors. SIGNIFICANCE: LTE may be a novel biomarker for metastasis, with transformative potential for personalized precision diagnostics of early-stage disease and improved patient survival.
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spelling pubmed-75180462020-10-09 Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma Holder, Ashley M. Ziemys, Arturas Front Oncol Oncology BACKGROUND: In staging patients with clinical stage I-II melanoma, the sentinel lymph node (SLN) is the most important prognostic indicator; however, the false negative rate of SLN biopsy (SLNB) is 15%. METHODS: Nine patients with clinical Stage I-II melanoma underwent SLNB with repeated intraoperative radiotracer measurements to determine lymphatic transport efficiency (LTE), which was correlated with clinicopathologic data. RESULTS: LTE demonstrated the potential to predict SLN status. LTE in patients with occult nodal metastasis is 40 times faster than those with negative SLNBs. There was no confounding of LTE by clinicopathologic factors. SIGNIFICANCE: LTE may be a novel biomarker for metastasis, with transformative potential for personalized precision diagnostics of early-stage disease and improved patient survival. Frontiers Media S.A. 2020-09-11 /pmc/articles/PMC7518046/ /pubmed/33042804 http://dx.doi.org/10.3389/fonc.2020.01607 Text en Copyright © 2020 Holder and Ziemys. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Holder, Ashley M.
Ziemys, Arturas
Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title_full Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title_fullStr Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title_full_unstemmed Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title_short Lymphatic Transport Efficiency Determines Metastatic Potential of Cutaneous Melanoma
title_sort lymphatic transport efficiency determines metastatic potential of cutaneous melanoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518046/
https://www.ncbi.nlm.nih.gov/pubmed/33042804
http://dx.doi.org/10.3389/fonc.2020.01607
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