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Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer
BACKGROUND: Precise methods for postoperative risk stratification to guide the administration of adjuvant chemotherapy (ACT) in localized colorectal cancer (CRC) are still lacking. Here, we conducted a prospective, observational, and multicenter study to investigate the utility of circulating tumor...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130394/ https://www.ncbi.nlm.nih.gov/pubmed/34001194 http://dx.doi.org/10.1186/s13045-021-01089-z |
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author | Chen, Gong Peng, Junjie Xiao, Qian Wu, Hao-Xiang Wu, Xiaojun Wang, Fulong Li, Liren Ding, Peirong Zhao, Qi Li, Yaqi Wang, Da Shao, Yang Bao, Hua Pan, Zhizhong Ding, Ke-Feng Cai, Sanjun Wang, Feng Xu, Rui-Hua |
author_facet | Chen, Gong Peng, Junjie Xiao, Qian Wu, Hao-Xiang Wu, Xiaojun Wang, Fulong Li, Liren Ding, Peirong Zhao, Qi Li, Yaqi Wang, Da Shao, Yang Bao, Hua Pan, Zhizhong Ding, Ke-Feng Cai, Sanjun Wang, Feng Xu, Rui-Hua |
author_sort | Chen, Gong |
collection | PubMed |
description | BACKGROUND: Precise methods for postoperative risk stratification to guide the administration of adjuvant chemotherapy (ACT) in localized colorectal cancer (CRC) are still lacking. Here, we conducted a prospective, observational, and multicenter study to investigate the utility of circulating tumor DNA (ctDNA) in predicting the recurrence risk. METHODS: From September 2017 to March 2020, 276 patients with stage II/III CRC were prospectively recruited in this study and 240 evaluable patients were retained for analysis, of which 1290 serial plasma samples were collected. Somatic variants in both the primary tumor and plasma were detected via a targeted sequencing panel of 425 cancer-related genes. Patients were treated and followed up per standard of care. RESULTS: Preoperatively, ctDNA was detectable in 154 of 240 patients (64.2%). At day 3–7 postoperation, ctDNA positivity was associated with remarkably high recurrence risk (hazard ratio [HR], 10.98; 95%CI, 5.31–22.72; P < 0.001). ctDNA clearance and recurrence-free status was achieved in 5 out of 17 ctDNA-positive patients who were subjected to ACT. Likewise, at the first sampling point after ACT, ctDNA-positive patients were 12 times more likely to experience recurrence (HR, 12.76; 95%CI, 5.39–30.19; P < 0.001). During surveillance after definitive therapy, ctDNA positivity was also associated with extremely high recurrence risk (HR, 32.02; 95%CI, 10.79–95.08; P < 0.001). In all multivariate analyses, ctDNA positivity remained the most significant and independent predictor of recurrence-free survival after adjusting for known clinicopathological risk factors. Serial ctDNA analyses identified recurrence with an overall accuracy of 92.0% and could detect disease recurrence ahead of radiological imaging with a mean lead time of 5.01 months. CONCLUSIONS: Postoperative serial ctDNA detection predicted high relapse risk and identified disease recurrence ahead of radiological imaging in patients with stage II/III CRC. ctDNA may be used to guide the decision-making in postsurgical management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01089-z. |
format | Online Article Text |
id | pubmed-8130394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81303942021-05-19 Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer Chen, Gong Peng, Junjie Xiao, Qian Wu, Hao-Xiang Wu, Xiaojun Wang, Fulong Li, Liren Ding, Peirong Zhao, Qi Li, Yaqi Wang, Da Shao, Yang Bao, Hua Pan, Zhizhong Ding, Ke-Feng Cai, Sanjun Wang, Feng Xu, Rui-Hua J Hematol Oncol Research BACKGROUND: Precise methods for postoperative risk stratification to guide the administration of adjuvant chemotherapy (ACT) in localized colorectal cancer (CRC) are still lacking. Here, we conducted a prospective, observational, and multicenter study to investigate the utility of circulating tumor DNA (ctDNA) in predicting the recurrence risk. METHODS: From September 2017 to March 2020, 276 patients with stage II/III CRC were prospectively recruited in this study and 240 evaluable patients were retained for analysis, of which 1290 serial plasma samples were collected. Somatic variants in both the primary tumor and plasma were detected via a targeted sequencing panel of 425 cancer-related genes. Patients were treated and followed up per standard of care. RESULTS: Preoperatively, ctDNA was detectable in 154 of 240 patients (64.2%). At day 3–7 postoperation, ctDNA positivity was associated with remarkably high recurrence risk (hazard ratio [HR], 10.98; 95%CI, 5.31–22.72; P < 0.001). ctDNA clearance and recurrence-free status was achieved in 5 out of 17 ctDNA-positive patients who were subjected to ACT. Likewise, at the first sampling point after ACT, ctDNA-positive patients were 12 times more likely to experience recurrence (HR, 12.76; 95%CI, 5.39–30.19; P < 0.001). During surveillance after definitive therapy, ctDNA positivity was also associated with extremely high recurrence risk (HR, 32.02; 95%CI, 10.79–95.08; P < 0.001). In all multivariate analyses, ctDNA positivity remained the most significant and independent predictor of recurrence-free survival after adjusting for known clinicopathological risk factors. Serial ctDNA analyses identified recurrence with an overall accuracy of 92.0% and could detect disease recurrence ahead of radiological imaging with a mean lead time of 5.01 months. CONCLUSIONS: Postoperative serial ctDNA detection predicted high relapse risk and identified disease recurrence ahead of radiological imaging in patients with stage II/III CRC. ctDNA may be used to guide the decision-making in postsurgical management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-021-01089-z. BioMed Central 2021-05-17 /pmc/articles/PMC8130394/ /pubmed/34001194 http://dx.doi.org/10.1186/s13045-021-01089-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chen, Gong Peng, Junjie Xiao, Qian Wu, Hao-Xiang Wu, Xiaojun Wang, Fulong Li, Liren Ding, Peirong Zhao, Qi Li, Yaqi Wang, Da Shao, Yang Bao, Hua Pan, Zhizhong Ding, Ke-Feng Cai, Sanjun Wang, Feng Xu, Rui-Hua Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title | Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title_full | Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title_fullStr | Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title_full_unstemmed | Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title_short | Postoperative circulating tumor DNA as markers of recurrence risk in stages II to III colorectal cancer |
title_sort | postoperative circulating tumor dna as markers of recurrence risk in stages ii to iii colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130394/ https://www.ncbi.nlm.nih.gov/pubmed/34001194 http://dx.doi.org/10.1186/s13045-021-01089-z |
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