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Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses

BACKGROUND: Circulating tumour DNA (ctDNA) has been established as a promising (prognostic) biomarker with the potential to personalise treatment in cancer patients. The objective of this systematic review is to provide an overview of the current literature and the future perspectives of ctDNA in no...

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Autores principales: van Rees, Jan M., Wullaert, Lissa, Grüter, Alexander A. J., Derraze, Yassmina, Tanis, Pieter J., Verheul, Henk M. W., Martens, John W. M., Wilting, Saskia M., Vink, Geraldine, van Vugt, Jeroen L. A., Beije, Nick, Verhoef, Cornelis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922989/
https://www.ncbi.nlm.nih.gov/pubmed/36793616
http://dx.doi.org/10.3389/fonc.2023.1083285
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author van Rees, Jan M.
Wullaert, Lissa
Grüter, Alexander A. J.
Derraze, Yassmina
Tanis, Pieter J.
Verheul, Henk M. W.
Martens, John W. M.
Wilting, Saskia M.
Vink, Geraldine
van Vugt, Jeroen L. A.
Beije, Nick
Verhoef, Cornelis
author_facet van Rees, Jan M.
Wullaert, Lissa
Grüter, Alexander A. J.
Derraze, Yassmina
Tanis, Pieter J.
Verheul, Henk M. W.
Martens, John W. M.
Wilting, Saskia M.
Vink, Geraldine
van Vugt, Jeroen L. A.
Beije, Nick
Verhoef, Cornelis
author_sort van Rees, Jan M.
collection PubMed
description BACKGROUND: Circulating tumour DNA (ctDNA) has been established as a promising (prognostic) biomarker with the potential to personalise treatment in cancer patients. The objective of this systematic review is to provide an overview of the current literature and the future perspectives of ctDNA in non-metastatic rectal cancer. METHODS: A comprehensive search for studies published prior to the 4(th) of October 2022 was conducted in Embase, Medline, Cochrane, Google scholar, and Web of Science. Only peer-reviewed original articles and ongoing clinical trials investigating the association between ctDNA and oncological outcomes in non-metastatic rectal cancer patients were included. Meta-analyses were performed to pool hazard ratios (HR) for recurrence-free survival (RFS). RESULTS: A total of 291 unique records were screened, of which 261 were original publications and 30 ongoing trials. Nineteen original publications were reviewed and discussed, of which seven provided sufficient data for meta-analyses on the association between the presence of post-treatment ctDNA and RFS. Results of the meta-analyses demonstrated that ctDNA analysis can be used to stratify patients into very high and low risk groups for recurrence, especially when detected after neoadjuvant treatment (HR for RFS: 9.3 [4.6 – 18.8]) and after surgery (HR for RFS: 15.5 [8.2 – 29.3]). Studies investigated different types of assays and used various techniques for the detection and quantification of ctDNA. CONCLUSIONS: This literature overview and meta-analyses provide evidence for the strong association between ctDNA and recurrent disease. Future research should focus on the feasibility of ctDNA-guided treatment and follow-up strategies in rectal cancer. A blueprint for agreed-upon timing, preprocessing, and assay techniques is needed to empower adaptation of ctDNA into daily practice.
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spelling pubmed-99229892023-02-14 Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses van Rees, Jan M. Wullaert, Lissa Grüter, Alexander A. J. Derraze, Yassmina Tanis, Pieter J. Verheul, Henk M. W. Martens, John W. M. Wilting, Saskia M. Vink, Geraldine van Vugt, Jeroen L. A. Beije, Nick Verhoef, Cornelis Front Oncol Oncology BACKGROUND: Circulating tumour DNA (ctDNA) has been established as a promising (prognostic) biomarker with the potential to personalise treatment in cancer patients. The objective of this systematic review is to provide an overview of the current literature and the future perspectives of ctDNA in non-metastatic rectal cancer. METHODS: A comprehensive search for studies published prior to the 4(th) of October 2022 was conducted in Embase, Medline, Cochrane, Google scholar, and Web of Science. Only peer-reviewed original articles and ongoing clinical trials investigating the association between ctDNA and oncological outcomes in non-metastatic rectal cancer patients were included. Meta-analyses were performed to pool hazard ratios (HR) for recurrence-free survival (RFS). RESULTS: A total of 291 unique records were screened, of which 261 were original publications and 30 ongoing trials. Nineteen original publications were reviewed and discussed, of which seven provided sufficient data for meta-analyses on the association between the presence of post-treatment ctDNA and RFS. Results of the meta-analyses demonstrated that ctDNA analysis can be used to stratify patients into very high and low risk groups for recurrence, especially when detected after neoadjuvant treatment (HR for RFS: 9.3 [4.6 – 18.8]) and after surgery (HR for RFS: 15.5 [8.2 – 29.3]). Studies investigated different types of assays and used various techniques for the detection and quantification of ctDNA. CONCLUSIONS: This literature overview and meta-analyses provide evidence for the strong association between ctDNA and recurrent disease. Future research should focus on the feasibility of ctDNA-guided treatment and follow-up strategies in rectal cancer. A blueprint for agreed-upon timing, preprocessing, and assay techniques is needed to empower adaptation of ctDNA into daily practice. Frontiers Media S.A. 2023-01-30 /pmc/articles/PMC9922989/ /pubmed/36793616 http://dx.doi.org/10.3389/fonc.2023.1083285 Text en Copyright © 2023 van Rees, Wullaert, Grüter, Derraze, Tanis, Verheul, Martens, Wilting, Vink, van Vugt, Beije and Verhoef https://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
van Rees, Jan M.
Wullaert, Lissa
Grüter, Alexander A. J.
Derraze, Yassmina
Tanis, Pieter J.
Verheul, Henk M. W.
Martens, John W. M.
Wilting, Saskia M.
Vink, Geraldine
van Vugt, Jeroen L. A.
Beije, Nick
Verhoef, Cornelis
Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title_full Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title_fullStr Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title_full_unstemmed Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title_short Circulating tumour DNA as biomarker for rectal cancer: A systematic review and meta-analyses
title_sort circulating tumour dna as biomarker for rectal cancer: a systematic review and meta-analyses
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922989/
https://www.ncbi.nlm.nih.gov/pubmed/36793616
http://dx.doi.org/10.3389/fonc.2023.1083285
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