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Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer

This study aimed to identify patients who benefit from radical surgery among those with rectal cancer who achieved clinical complete response (cCR). Patients with locally advanced rectal cancer (LARC; stage II/III) who achieved cCR after neoadjuvant chemoradiotherapy (nCRT) were included (n = 212)....

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Autores principales: Zhang, Shu, Zhang, Rong, Li, Rong‐zhen, Wang, Qiao‐xuan, Chang, Hui, Ding, Pei‐rong, Li, Li‐ren, Wu, Xiao‐jun, Chen, Gong, Zeng, Zhi‐fan, Xiao, Wei‐wei, Gao, Yuan‐hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409289/
https://www.ncbi.nlm.nih.gov/pubmed/34146368
http://dx.doi.org/10.1111/cas.15039
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author Zhang, Shu
Zhang, Rong
Li, Rong‐zhen
Wang, Qiao‐xuan
Chang, Hui
Ding, Pei‐rong
Li, Li‐ren
Wu, Xiao‐jun
Chen, Gong
Zeng, Zhi‐fan
Xiao, Wei‐wei
Gao, Yuan‐hong
author_facet Zhang, Shu
Zhang, Rong
Li, Rong‐zhen
Wang, Qiao‐xuan
Chang, Hui
Ding, Pei‐rong
Li, Li‐ren
Wu, Xiao‐jun
Chen, Gong
Zeng, Zhi‐fan
Xiao, Wei‐wei
Gao, Yuan‐hong
author_sort Zhang, Shu
collection PubMed
description This study aimed to identify patients who benefit from radical surgery among those with rectal cancer who achieved clinical complete response (cCR). Patients with locally advanced rectal cancer (LARC; stage II/III) who achieved cCR after neoadjuvant chemoradiotherapy (nCRT) were included (n = 212). Univariate/multivariate Cox analysis was performed to validate predictors for distant metastasis‐free survival (DMFS). A decision tree was generated using recursive partitioning analysis (RPA) to categorize patients into different risk stratifications. Total mesorectal excision (TME) was compared with the watch‐and‐wait (W&W) strategy in each risk group. Two molecular predicators of CEA and CA19‐9 were selected to establish the RPA‐based risk stratification, categorizing LARC patients into low‐risk (n = 139; CA19‐9 < 35 U/mL and CEA < 5 ng/mL) and high‐risk (n = 73; CA19‐9 ≥ 35 U/mL or CEA ≥5 ng/mL) groups. Superior 5‐y DMFS was observed in the low‐risk group vs. the high‐risk group (92.9% vs. 76.2%, P = .002). Low‐risk LARC patients who underwent TME had significantly improved 5‐y DMFS compared with their counterparts receiving the W&W strategy (95.9% vs. 84.3%; P = .028). No significant survival difference was observed in high‐risk patients receiving the 2 treatment modalities (77.9% vs. 94.1%; P = .143). LARC patients with cCR who had both baseline CA19‐9 < 35 U/mL and CEA < 5 ng/mL may benefit from radical surgery.
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spelling pubmed-84092892021-09-03 Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer Zhang, Shu Zhang, Rong Li, Rong‐zhen Wang, Qiao‐xuan Chang, Hui Ding, Pei‐rong Li, Li‐ren Wu, Xiao‐jun Chen, Gong Zeng, Zhi‐fan Xiao, Wei‐wei Gao, Yuan‐hong Cancer Sci Original Articles This study aimed to identify patients who benefit from radical surgery among those with rectal cancer who achieved clinical complete response (cCR). Patients with locally advanced rectal cancer (LARC; stage II/III) who achieved cCR after neoadjuvant chemoradiotherapy (nCRT) were included (n = 212). Univariate/multivariate Cox analysis was performed to validate predictors for distant metastasis‐free survival (DMFS). A decision tree was generated using recursive partitioning analysis (RPA) to categorize patients into different risk stratifications. Total mesorectal excision (TME) was compared with the watch‐and‐wait (W&W) strategy in each risk group. Two molecular predicators of CEA and CA19‐9 were selected to establish the RPA‐based risk stratification, categorizing LARC patients into low‐risk (n = 139; CA19‐9 < 35 U/mL and CEA < 5 ng/mL) and high‐risk (n = 73; CA19‐9 ≥ 35 U/mL or CEA ≥5 ng/mL) groups. Superior 5‐y DMFS was observed in the low‐risk group vs. the high‐risk group (92.9% vs. 76.2%, P = .002). Low‐risk LARC patients who underwent TME had significantly improved 5‐y DMFS compared with their counterparts receiving the W&W strategy (95.9% vs. 84.3%; P = .028). No significant survival difference was observed in high‐risk patients receiving the 2 treatment modalities (77.9% vs. 94.1%; P = .143). LARC patients with cCR who had both baseline CA19‐9 < 35 U/mL and CEA < 5 ng/mL may benefit from radical surgery. John Wiley and Sons Inc. 2021-07-21 2021-09 /pmc/articles/PMC8409289/ /pubmed/34146368 http://dx.doi.org/10.1111/cas.15039 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Zhang, Shu
Zhang, Rong
Li, Rong‐zhen
Wang, Qiao‐xuan
Chang, Hui
Ding, Pei‐rong
Li, Li‐ren
Wu, Xiao‐jun
Chen, Gong
Zeng, Zhi‐fan
Xiao, Wei‐wei
Gao, Yuan‐hong
Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title_full Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title_fullStr Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title_full_unstemmed Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title_short Beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
title_sort beneficiaries of radical surgery among clinical complete responders to neoadjuvant chemoradiotherapy in rectal cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409289/
https://www.ncbi.nlm.nih.gov/pubmed/34146368
http://dx.doi.org/10.1111/cas.15039
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