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Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy

BACKGROUND: Lymphocytic density in rectal cancer has been reported to be associated with therapeutic response, but the role of the lymphocytic distribution pattern remains to be determined. This study aimed to evaluate the association between the distribution and density of lymphocytes in rectal-can...

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Autores principales: Lai, Sicong, Lou, Xiaoying, Fan, Xinjuan, Sun, Weipeng, Deng, Yanhong, Wang, Jianping, Huang, Yan, Dou, Ruoxu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793145/
https://www.ncbi.nlm.nih.gov/pubmed/33442477
http://dx.doi.org/10.1093/gastro/goaa016
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author Lai, Sicong
Lou, Xiaoying
Fan, Xinjuan
Sun, Weipeng
Deng, Yanhong
Wang, Jianping
Huang, Yan
Dou, Ruoxu
author_facet Lai, Sicong
Lou, Xiaoying
Fan, Xinjuan
Sun, Weipeng
Deng, Yanhong
Wang, Jianping
Huang, Yan
Dou, Ruoxu
author_sort Lai, Sicong
collection PubMed
description BACKGROUND: Lymphocytic density in rectal cancer has been reported to be associated with therapeutic response, but the role of the lymphocytic distribution pattern remains to be determined. This study aimed to evaluate the association between the distribution and density of lymphocytes in rectal-cancer tissue with tumor response to neoadjuvant therapy. METHODS: We retrospectively analysed 134 patients with rectal cancer receiving neoadjuvant therapy within a prospectively maintained cohort. Pretherapeutic biopsy samples were stained with immunohistochemistry (CD4 and CD8). Densities of intratumoral periglandular lymphocytes (IPLs) and tumor-infiltrating lymphocytes (TILs) were assessed separately. Logistic-regression analysis was used to assess associations of lymphocyte densities with tumor regression grade (TRG), controlling for clinicopathological, molecular, and regimen features. RESULTS: Compared with cases in the lowest quartile of CD8(+) TILs, those in the highest quartile were significantly associated with better TRG (multivariate odds ratio, 0.23; 95% confidence interval, 0.07 to 0.76; P < 0.001). In contrast, CD8(+) IPLs, CD4(+) IPLs, and CD4(+) TILs were not significantly associated with TRG (P = 0.033, 0.156, and 0.170, respectively). Sensitivity analyses detected no interaction between CD8(+) TILs and regimen of neoadjuvant radiation (P(interaction) = 0.831) or chemotherapy (P(interaction) = 0.879) on TRG. CONCLUSIONS: Our data suggest that CD8(+) TILs, but not IPLs, are independently associated with response to neoadjuvant therapy, regardless of the regimen of radiation or chemotherapy.
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spelling pubmed-77931452021-01-12 Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy Lai, Sicong Lou, Xiaoying Fan, Xinjuan Sun, Weipeng Deng, Yanhong Wang, Jianping Huang, Yan Dou, Ruoxu Gastroenterol Rep (Oxf) Original Articles BACKGROUND: Lymphocytic density in rectal cancer has been reported to be associated with therapeutic response, but the role of the lymphocytic distribution pattern remains to be determined. This study aimed to evaluate the association between the distribution and density of lymphocytes in rectal-cancer tissue with tumor response to neoadjuvant therapy. METHODS: We retrospectively analysed 134 patients with rectal cancer receiving neoadjuvant therapy within a prospectively maintained cohort. Pretherapeutic biopsy samples were stained with immunohistochemistry (CD4 and CD8). Densities of intratumoral periglandular lymphocytes (IPLs) and tumor-infiltrating lymphocytes (TILs) were assessed separately. Logistic-regression analysis was used to assess associations of lymphocyte densities with tumor regression grade (TRG), controlling for clinicopathological, molecular, and regimen features. RESULTS: Compared with cases in the lowest quartile of CD8(+) TILs, those in the highest quartile were significantly associated with better TRG (multivariate odds ratio, 0.23; 95% confidence interval, 0.07 to 0.76; P < 0.001). In contrast, CD8(+) IPLs, CD4(+) IPLs, and CD4(+) TILs were not significantly associated with TRG (P = 0.033, 0.156, and 0.170, respectively). Sensitivity analyses detected no interaction between CD8(+) TILs and regimen of neoadjuvant radiation (P(interaction) = 0.831) or chemotherapy (P(interaction) = 0.879) on TRG. CONCLUSIONS: Our data suggest that CD8(+) TILs, but not IPLs, are independently associated with response to neoadjuvant therapy, regardless of the regimen of radiation or chemotherapy. Oxford University Press 2020-06-12 /pmc/articles/PMC7793145/ /pubmed/33442477 http://dx.doi.org/10.1093/gastro/goaa016 Text en © The Author(s) 2020. Published by Oxford University Press and Sixth Affiliated Hospital of Sun Yat-sen University http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Lai, Sicong
Lou, Xiaoying
Fan, Xinjuan
Sun, Weipeng
Deng, Yanhong
Wang, Jianping
Huang, Yan
Dou, Ruoxu
Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title_full Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title_fullStr Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title_full_unstemmed Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title_short Density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
title_sort density and distribution of lymphocytes in pretherapeutic rectal cancer and response to neoadjuvant therapy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793145/
https://www.ncbi.nlm.nih.gov/pubmed/33442477
http://dx.doi.org/10.1093/gastro/goaa016
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