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A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging
BACKGROUND: Current clinico-pathological American Joint Committee on Cancer (AJCC) staging of primary cutaneous melanoma is limited in its ability to determine clinical outcome, and complementary biomarkers are not available for routine prognostic assessment. We therefore adapted a gene signature, p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649804/ https://www.ncbi.nlm.nih.gov/pubmed/31360859 http://dx.doi.org/10.1093/jncics/pky032 |
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author | Brunner, Georg Heinecke, Achim Falk, Thomas M Ertas, Beyhan Blödorn-Schlicht, Norbert Schulze, Hans-Joachim Suter, Ludwig Atzpodien, Jens Berking, Carola |
author_facet | Brunner, Georg Heinecke, Achim Falk, Thomas M Ertas, Beyhan Blödorn-Schlicht, Norbert Schulze, Hans-Joachim Suter, Ludwig Atzpodien, Jens Berking, Carola |
author_sort | Brunner, Georg |
collection | PubMed |
description | BACKGROUND: Current clinico-pathological American Joint Committee on Cancer (AJCC) staging of primary cutaneous melanoma is limited in its ability to determine clinical outcome, and complementary biomarkers are not available for routine prognostic assessment. We therefore adapted a gene signature, previously identified in fresh-frozen (FF) melanomas and adjacent stroma, to formalin-fixed paraffin-embedded (FFPE) melanomas. The aim was to develop a gene expression profiling (GEP) score to define patient survival probability at the time of first diagnosis. METHODS: Expression of 11 FF melanoma signature genes was quantified by reverse transcription polymerase chain reaction in an FFPE melanoma training cohort (n = 125), corresponding to the combined FF melanoma training and validation cohorts. The resulting GEP score was validated technically and clinically in an independent FFPE melanoma cohort (n = 211). All statistical tests were two-sided. RESULTS: We identified a prognostic eight-gene signature in the tumor area (tumor and adjacent tissue) of AJCC stage I–III melanomas. A signature-based GEP score correlated with melanoma-specific survival (MSS; Kaplan-Meier analysis: P < .0001) was independent of tumor stage (multivariable regression analysis: P = .0032) and stroma content (<5%–90%) and complemented conventional AJCC staging (receiver operating characteristic curve analysis: area under the curve = 0.91). In the clinical validation cohort, the GEP score remained statistically significant (P = .0131) in a multivariable analysis accounting for conventional staging. The GEP score was technically robust (reproducibility: 93%; n = 84) and clinically useful, as a binary as well as a continuous score, in predicting stage-specific patient MSS. CONCLUSIONS: The GEP score is a clinically significant prognostic tool, contributes additional information regarding the MSS of melanoma patients, and complements conventional staging. |
format | Online Article Text |
id | pubmed-6649804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66498042019-07-29 A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging Brunner, Georg Heinecke, Achim Falk, Thomas M Ertas, Beyhan Blödorn-Schlicht, Norbert Schulze, Hans-Joachim Suter, Ludwig Atzpodien, Jens Berking, Carola JNCI Cancer Spectr Article BACKGROUND: Current clinico-pathological American Joint Committee on Cancer (AJCC) staging of primary cutaneous melanoma is limited in its ability to determine clinical outcome, and complementary biomarkers are not available for routine prognostic assessment. We therefore adapted a gene signature, previously identified in fresh-frozen (FF) melanomas and adjacent stroma, to formalin-fixed paraffin-embedded (FFPE) melanomas. The aim was to develop a gene expression profiling (GEP) score to define patient survival probability at the time of first diagnosis. METHODS: Expression of 11 FF melanoma signature genes was quantified by reverse transcription polymerase chain reaction in an FFPE melanoma training cohort (n = 125), corresponding to the combined FF melanoma training and validation cohorts. The resulting GEP score was validated technically and clinically in an independent FFPE melanoma cohort (n = 211). All statistical tests were two-sided. RESULTS: We identified a prognostic eight-gene signature in the tumor area (tumor and adjacent tissue) of AJCC stage I–III melanomas. A signature-based GEP score correlated with melanoma-specific survival (MSS; Kaplan-Meier analysis: P < .0001) was independent of tumor stage (multivariable regression analysis: P = .0032) and stroma content (<5%–90%) and complemented conventional AJCC staging (receiver operating characteristic curve analysis: area under the curve = 0.91). In the clinical validation cohort, the GEP score remained statistically significant (P = .0131) in a multivariable analysis accounting for conventional staging. The GEP score was technically robust (reproducibility: 93%; n = 84) and clinically useful, as a binary as well as a continuous score, in predicting stage-specific patient MSS. CONCLUSIONS: The GEP score is a clinically significant prognostic tool, contributes additional information regarding the MSS of melanoma patients, and complements conventional staging. Oxford University Press 2018-07-23 /pmc/articles/PMC6649804/ /pubmed/31360859 http://dx.doi.org/10.1093/jncics/pky032 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Brunner, Georg Heinecke, Achim Falk, Thomas M Ertas, Beyhan Blödorn-Schlicht, Norbert Schulze, Hans-Joachim Suter, Ludwig Atzpodien, Jens Berking, Carola A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title | A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title_full | A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title_fullStr | A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title_full_unstemmed | A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title_short | A Prognostic Gene Signature Expressed in Primary Cutaneous Melanoma: Synergism With Conventional Staging |
title_sort | prognostic gene signature expressed in primary cutaneous melanoma: synergism with conventional staging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649804/ https://www.ncbi.nlm.nih.gov/pubmed/31360859 http://dx.doi.org/10.1093/jncics/pky032 |
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