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Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis

BACKGROUND: Circulating tumor DNA (ctDNA) is an emerging biomarker for locally advanced rectal cancer (LARC), giving hope for stratified treatment. As the completed studies have small sample sizes and different experimental methods, systematic review and meta‐analysis were performed to explore their...

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Autores principales: Mi, Junjie, Wang, Rong, Han, Xiaofang, Ma, Ruijun, Zhao, Danyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523996/
https://www.ncbi.nlm.nih.gov/pubmed/37553845
http://dx.doi.org/10.1002/cam4.6434
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author Mi, Junjie
Wang, Rong
Han, Xiaofang
Ma, Ruijun
Zhao, Danyu
author_facet Mi, Junjie
Wang, Rong
Han, Xiaofang
Ma, Ruijun
Zhao, Danyu
author_sort Mi, Junjie
collection PubMed
description BACKGROUND: Circulating tumor DNA (ctDNA) is an emerging biomarker for locally advanced rectal cancer (LARC), giving hope for stratified treatment. As the completed studies have small sample sizes and different experimental methods, systematic review and meta‐analysis were performed to explore their role in predicting pathological complete response (pCR), tumor recurrence, and prognosis. METHODS: PubMed, Embase, and the Web of Science were searched for potentially eligible studies published up to September 6, 2022. Pooled relative risk (RR) was calculated to predict pCR and tumor recurrence, and pooled hazard ratio (HR) was calculated to evaluate the prognosis of overall survival (OS), recurrence‐free survival (RFS), and metastasis‐free survival (MRS). RESULTS: Twelve studies published between 2018 and 2022 included 931 patients, and 2544 serum samples were eventually included in the meta‐analysis. The pooled revealed that ctDNA‐negative patients were more likely to have a pCR (RR = 1.64, 95% confidence interval [CI]: 1.26–2.12). The pooled revealed that ctDNA‐positive patients were at high risk of recurrence (RR = 3.37, 95% CI: 2.34–4.85) and had a poorer prognosis for OS (HR = 3.03, 95% CI: 1.86–4.95), RFS (HR = 7.08, 95% CI: 4.12–12.14), and MRS (HR = 2.77, 95% CI: 2.01–3.83). CONCLUSION: ctDNA may be useful for stratifying treatment and assessing prognosis in patients with LARC, but its clinical application still needs to be confirmed in a prospective multicenter study with large samples.
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spelling pubmed-105239962023-09-28 Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis Mi, Junjie Wang, Rong Han, Xiaofang Ma, Ruijun Zhao, Danyu Cancer Med RESEARCH ARTICLES BACKGROUND: Circulating tumor DNA (ctDNA) is an emerging biomarker for locally advanced rectal cancer (LARC), giving hope for stratified treatment. As the completed studies have small sample sizes and different experimental methods, systematic review and meta‐analysis were performed to explore their role in predicting pathological complete response (pCR), tumor recurrence, and prognosis. METHODS: PubMed, Embase, and the Web of Science were searched for potentially eligible studies published up to September 6, 2022. Pooled relative risk (RR) was calculated to predict pCR and tumor recurrence, and pooled hazard ratio (HR) was calculated to evaluate the prognosis of overall survival (OS), recurrence‐free survival (RFS), and metastasis‐free survival (MRS). RESULTS: Twelve studies published between 2018 and 2022 included 931 patients, and 2544 serum samples were eventually included in the meta‐analysis. The pooled revealed that ctDNA‐negative patients were more likely to have a pCR (RR = 1.64, 95% confidence interval [CI]: 1.26–2.12). The pooled revealed that ctDNA‐positive patients were at high risk of recurrence (RR = 3.37, 95% CI: 2.34–4.85) and had a poorer prognosis for OS (HR = 3.03, 95% CI: 1.86–4.95), RFS (HR = 7.08, 95% CI: 4.12–12.14), and MRS (HR = 2.77, 95% CI: 2.01–3.83). CONCLUSION: ctDNA may be useful for stratifying treatment and assessing prognosis in patients with LARC, but its clinical application still needs to be confirmed in a prospective multicenter study with large samples. John Wiley and Sons Inc. 2023-08-08 /pmc/articles/PMC10523996/ /pubmed/37553845 http://dx.doi.org/10.1002/cam4.6434 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Mi, Junjie
Wang, Rong
Han, Xiaofang
Ma, Ruijun
Zhao, Danyu
Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title_full Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title_fullStr Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title_full_unstemmed Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title_short Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta‐analysis
title_sort treatment stratification and prognosis assessment using circulating tumor dna in locally advanced rectal cancer: a systematic review and meta‐analysis
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523996/
https://www.ncbi.nlm.nih.gov/pubmed/37553845
http://dx.doi.org/10.1002/cam4.6434
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