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Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review

BACKGROUND: Biomarkers that can predict the prognosis of colorectal cancer (CRC) patients and that can stratify high-risk early stage patients from low-risk early stage patients are urgently needed for better management of CRC. During the last decades, a large variety of prognostic DNA methylation m...

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Autores principales: Draht, Muriel X. G., Goudkade, Danny, Koch, Alexander, Grabsch, Heike I., Weijenberg, Matty P., van Engeland, Manon, Melotte, Veerle, Smits, Kim M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851322/
https://www.ncbi.nlm.nih.gov/pubmed/29564023
http://dx.doi.org/10.1186/s13148-018-0461-8
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author Draht, Muriel X. G.
Goudkade, Danny
Koch, Alexander
Grabsch, Heike I.
Weijenberg, Matty P.
van Engeland, Manon
Melotte, Veerle
Smits, Kim M.
author_facet Draht, Muriel X. G.
Goudkade, Danny
Koch, Alexander
Grabsch, Heike I.
Weijenberg, Matty P.
van Engeland, Manon
Melotte, Veerle
Smits, Kim M.
author_sort Draht, Muriel X. G.
collection PubMed
description BACKGROUND: Biomarkers that can predict the prognosis of colorectal cancer (CRC) patients and that can stratify high-risk early stage patients from low-risk early stage patients are urgently needed for better management of CRC. During the last decades, a large variety of prognostic DNA methylation markers has been published in the literature. However, to date, none of these markers are used in clinical practice. METHODS: To obtain an overview of the number of published prognostic methylation markers for CRC, the number of markers that was validated independently, and the current level of evidence (LoE), we conducted a systematic review of PubMed, EMBASE, and MEDLINE. In addition, we scored studies based on the REMARK guidelines that were established in order to attain more transparency and complete reporting of prognostic biomarker studies. Eighty-three studies reporting on 123 methylation markers fulfilled the study entry criteria and were scored according to REMARK. RESULTS: Sixty-three studies investigated single methylation markers, whereas 20 studies reported combinations of methylation markers. We observed substantial variation regarding the reporting of sample sizes and patient characteristics, statistical analyses, and methodology. The median (range) REMARK score for the studies was 10.7 points (4.5 to 17.5) out of a maximum of 20 possible points. The median REMARK score was lower in studies, which reported a p value below 0.05 versus those, which did not (p = 0.005). A borderline statistically significant association was observed between the reported p value of the survival analysis and the size of the study population (p = 0.051). Only 23 out of 123 markers (17%) were investigated in two or more study series. For 12 markers, and two multimarker panels, consistent results were reported in two or more study series. For four markers, the current LoE is level II, for all other markers, the LoE is lower. CONCLUSION: This systematic review reflects that adequate reporting according to REMARK and validation of prognostic methylation markers is absent in the majority of CRC methylation marker studies. However, this systematic review provides a comprehensive overview of published prognostic methylation markers for CRC and highlights the most promising markers that have been published in the last two decades. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0461-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-58513222018-03-21 Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review Draht, Muriel X. G. Goudkade, Danny Koch, Alexander Grabsch, Heike I. Weijenberg, Matty P. van Engeland, Manon Melotte, Veerle Smits, Kim M. Clin Epigenetics Review BACKGROUND: Biomarkers that can predict the prognosis of colorectal cancer (CRC) patients and that can stratify high-risk early stage patients from low-risk early stage patients are urgently needed for better management of CRC. During the last decades, a large variety of prognostic DNA methylation markers has been published in the literature. However, to date, none of these markers are used in clinical practice. METHODS: To obtain an overview of the number of published prognostic methylation markers for CRC, the number of markers that was validated independently, and the current level of evidence (LoE), we conducted a systematic review of PubMed, EMBASE, and MEDLINE. In addition, we scored studies based on the REMARK guidelines that were established in order to attain more transparency and complete reporting of prognostic biomarker studies. Eighty-three studies reporting on 123 methylation markers fulfilled the study entry criteria and were scored according to REMARK. RESULTS: Sixty-three studies investigated single methylation markers, whereas 20 studies reported combinations of methylation markers. We observed substantial variation regarding the reporting of sample sizes and patient characteristics, statistical analyses, and methodology. The median (range) REMARK score for the studies was 10.7 points (4.5 to 17.5) out of a maximum of 20 possible points. The median REMARK score was lower in studies, which reported a p value below 0.05 versus those, which did not (p = 0.005). A borderline statistically significant association was observed between the reported p value of the survival analysis and the size of the study population (p = 0.051). Only 23 out of 123 markers (17%) were investigated in two or more study series. For 12 markers, and two multimarker panels, consistent results were reported in two or more study series. For four markers, the current LoE is level II, for all other markers, the LoE is lower. CONCLUSION: This systematic review reflects that adequate reporting according to REMARK and validation of prognostic methylation markers is absent in the majority of CRC methylation marker studies. However, this systematic review provides a comprehensive overview of published prognostic methylation markers for CRC and highlights the most promising markers that have been published in the last two decades. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0461-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-14 /pmc/articles/PMC5851322/ /pubmed/29564023 http://dx.doi.org/10.1186/s13148-018-0461-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Draht, Muriel X. G.
Goudkade, Danny
Koch, Alexander
Grabsch, Heike I.
Weijenberg, Matty P.
van Engeland, Manon
Melotte, Veerle
Smits, Kim M.
Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title_full Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title_fullStr Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title_full_unstemmed Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title_short Prognostic DNA methylation markers for sporadic colorectal cancer: a systematic review
title_sort prognostic dna methylation markers for sporadic colorectal cancer: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851322/
https://www.ncbi.nlm.nih.gov/pubmed/29564023
http://dx.doi.org/10.1186/s13148-018-0461-8
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