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Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients

SIMPLE SUMMARY: Circulating tumor cells (CTCs) originating from cutaneous melanoma patients have been studied for several decades as surrogates for real-time clinical status and disease outcomes. Here, we will review clinical studies from the last 15 years that assessed CTCs and disease outcomes for...

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Autores principales: Shoji, Yoshiaki, Bustos, Matias A., Gross, Rebecca, Hoon, Dave S. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870206/
https://www.ncbi.nlm.nih.gov/pubmed/35205608
http://dx.doi.org/10.3390/cancers14040859
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author Shoji, Yoshiaki
Bustos, Matias A.
Gross, Rebecca
Hoon, Dave S. B.
author_facet Shoji, Yoshiaki
Bustos, Matias A.
Gross, Rebecca
Hoon, Dave S. B.
author_sort Shoji, Yoshiaki
collection PubMed
description SIMPLE SUMMARY: Circulating tumor cells (CTCs) originating from cutaneous melanoma patients have been studied for several decades as surrogates for real-time clinical status and disease outcomes. Here, we will review clinical studies from the last 15 years that assessed CTCs and disease outcomes for melanoma patients. Assessment of multiple molecular melanoma-associated antigen (MAA) markers by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was the most common assay allowing for the improvement of assay sensitivity, to address tumor heterogeneity, and to predict patient outcomes. Multicenter studies demonstrate the utility of CTC assays reducing the bias observed in single-center trials. Recent development of CTC enrichment platforms has provided reproducible methods. CTC assessment enables both multiple mRNAs and DNAs genomic profiling. CTC provides specific important translational information on tumor progression, prediction of treatment response, and survival outcomes for cutaneous melanoma patients. ABSTRACT: Circulating tumor cells (CTCs) have been studied using multiple technical approaches for interrogating various cancers, as they allow for the real-time assessment of tumor progression, disease recurrence, treatment response, and tumor molecular profiling without the need for a tumor tissue biopsy. Here, we will review studies from the last 15 years on the assessment of CTCs in cutaneous melanoma patients in relation to different clinical outcomes. The focus will be on CTC detection in blood samples obtained from cutaneous melanoma patients of different clinical stages and treatments utilizing multiple platforms. Assessment of multiple molecular melanoma-associated antigen (MAA) markers by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was the most common assay allowing for the improvement of assay sensitivity, tumor heterogeneity, and to predict patient outcomes. Multicenter studies demonstrate the utility of CTC assays reducing the bias observed in single- center trials. The recent development of CTC enrichment platforms has provided reproducible methods. CTC assessment enables both multiple mRNAs and DNAs genomic aberration profiling. CTC provides specific important translational information on tumor progression, prediction of treatment response, and survival outcomes for cutaneous melanoma patients. The molecular studies on melanoma CTCs have provided and may set standards for other solid tumor CTC analyses.
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spelling pubmed-88702062022-02-25 Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients Shoji, Yoshiaki Bustos, Matias A. Gross, Rebecca Hoon, Dave S. B. Cancers (Basel) Review SIMPLE SUMMARY: Circulating tumor cells (CTCs) originating from cutaneous melanoma patients have been studied for several decades as surrogates for real-time clinical status and disease outcomes. Here, we will review clinical studies from the last 15 years that assessed CTCs and disease outcomes for melanoma patients. Assessment of multiple molecular melanoma-associated antigen (MAA) markers by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was the most common assay allowing for the improvement of assay sensitivity, to address tumor heterogeneity, and to predict patient outcomes. Multicenter studies demonstrate the utility of CTC assays reducing the bias observed in single-center trials. Recent development of CTC enrichment platforms has provided reproducible methods. CTC assessment enables both multiple mRNAs and DNAs genomic profiling. CTC provides specific important translational information on tumor progression, prediction of treatment response, and survival outcomes for cutaneous melanoma patients. ABSTRACT: Circulating tumor cells (CTCs) have been studied using multiple technical approaches for interrogating various cancers, as they allow for the real-time assessment of tumor progression, disease recurrence, treatment response, and tumor molecular profiling without the need for a tumor tissue biopsy. Here, we will review studies from the last 15 years on the assessment of CTCs in cutaneous melanoma patients in relation to different clinical outcomes. The focus will be on CTC detection in blood samples obtained from cutaneous melanoma patients of different clinical stages and treatments utilizing multiple platforms. Assessment of multiple molecular melanoma-associated antigen (MAA) markers by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was the most common assay allowing for the improvement of assay sensitivity, tumor heterogeneity, and to predict patient outcomes. Multicenter studies demonstrate the utility of CTC assays reducing the bias observed in single- center trials. The recent development of CTC enrichment platforms has provided reproducible methods. CTC assessment enables both multiple mRNAs and DNAs genomic aberration profiling. CTC provides specific important translational information on tumor progression, prediction of treatment response, and survival outcomes for cutaneous melanoma patients. The molecular studies on melanoma CTCs have provided and may set standards for other solid tumor CTC analyses. MDPI 2022-02-09 /pmc/articles/PMC8870206/ /pubmed/35205608 http://dx.doi.org/10.3390/cancers14040859 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Shoji, Yoshiaki
Bustos, Matias A.
Gross, Rebecca
Hoon, Dave S. B.
Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title_full Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title_fullStr Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title_full_unstemmed Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title_short Recent Developments of Circulating Tumor Cell Analysis for Monitoring Cutaneous Melanoma Patients
title_sort recent developments of circulating tumor cell analysis for monitoring cutaneous melanoma patients
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870206/
https://www.ncbi.nlm.nih.gov/pubmed/35205608
http://dx.doi.org/10.3390/cancers14040859
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