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Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer
Following standard neoadjuvant chemoradiotherapy and total mesorectal excision, some patients with locally advanced rectal cancer achieve good response (pathological T0–2N0), while others show nonresponse (pathological T3–4N0 or node‐positive). To date, the clinicopathological predictors of good res...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290248/ https://www.ncbi.nlm.nih.gov/pubmed/34128335 http://dx.doi.org/10.1002/cam4.4051 |
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author | Pang, Xiaolin Gao, Yuanhong Yi, Hanchen Liu, Hailing Liu, Shuai Zheng, Jian |
author_facet | Pang, Xiaolin Gao, Yuanhong Yi, Hanchen Liu, Hailing Liu, Shuai Zheng, Jian |
author_sort | Pang, Xiaolin |
collection | PubMed |
description | Following standard neoadjuvant chemoradiotherapy and total mesorectal excision, some patients with locally advanced rectal cancer achieve good response (pathological T0–2N0), while others show nonresponse (pathological T3–4N0 or node‐positive). To date, the clinicopathological predictors of good response and the necessity of adjuvant chemotherapy treatment (ACT) in good responders remain unclear. In this retrospective study, clinicopathological characteristics were surveyed to investigate the correlation with good response; furthermore, a propensity score matching (PSM) model was designed to balance the confounding factors between good responders treated with ACT or observation. A total of 2255 patients were enrolled, including 1069 good responders and 1186 nonresponders. The results of the survival analysis showed a good response predicted a better 3‐year prognosis (p < 0.001). The logistic regression analysis showed less advanced T and N stages (T3 vs. T4; N0 vs. N1–2), more neoadjuvant chemotherapy (nCT) cycles (≥4 vs. 1–3), and delayed surgery (≥8 weeks vs. <8 weeks) were independent predictors of a good response (p < 0.05). Especially, patients treated with both more nCT cycles and a delay in surgery included the greatest number of good responders (p < 0.001). For good responders, after PSM (1:3), 235 observation cases were matched to 705 ACT cases. As compared with observation, ACT had no greater impact on prognosis analysis (p > 0.05). In conclusion, more cycles of nCT and a delay in surgery predicted a better response, and the delivery of ACT might be omitted in good responders. |
format | Online Article Text |
id | pubmed-8290248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82902482021-07-21 Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer Pang, Xiaolin Gao, Yuanhong Yi, Hanchen Liu, Hailing Liu, Shuai Zheng, Jian Cancer Med Clinical Cancer Research Following standard neoadjuvant chemoradiotherapy and total mesorectal excision, some patients with locally advanced rectal cancer achieve good response (pathological T0–2N0), while others show nonresponse (pathological T3–4N0 or node‐positive). To date, the clinicopathological predictors of good response and the necessity of adjuvant chemotherapy treatment (ACT) in good responders remain unclear. In this retrospective study, clinicopathological characteristics were surveyed to investigate the correlation with good response; furthermore, a propensity score matching (PSM) model was designed to balance the confounding factors between good responders treated with ACT or observation. A total of 2255 patients were enrolled, including 1069 good responders and 1186 nonresponders. The results of the survival analysis showed a good response predicted a better 3‐year prognosis (p < 0.001). The logistic regression analysis showed less advanced T and N stages (T3 vs. T4; N0 vs. N1–2), more neoadjuvant chemotherapy (nCT) cycles (≥4 vs. 1–3), and delayed surgery (≥8 weeks vs. <8 weeks) were independent predictors of a good response (p < 0.05). Especially, patients treated with both more nCT cycles and a delay in surgery included the greatest number of good responders (p < 0.001). For good responders, after PSM (1:3), 235 observation cases were matched to 705 ACT cases. As compared with observation, ACT had no greater impact on prognosis analysis (p > 0.05). In conclusion, more cycles of nCT and a delay in surgery predicted a better response, and the delivery of ACT might be omitted in good responders. John Wiley and Sons Inc. 2021-06-15 /pmc/articles/PMC8290248/ /pubmed/34128335 http://dx.doi.org/10.1002/cam4.4051 Text en © 2021 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 | Clinical Cancer Research Pang, Xiaolin Gao, Yuanhong Yi, Hanchen Liu, Hailing Liu, Shuai Zheng, Jian Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title | Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title_full | Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title_fullStr | Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title_full_unstemmed | Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title_short | Associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
title_sort | associations between clinical characteristics and tumor response to neoadjuvant chemoradiotherapy in rectal cancer |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290248/ https://www.ncbi.nlm.nih.gov/pubmed/34128335 http://dx.doi.org/10.1002/cam4.4051 |
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