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Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer

Currently, tumor-infiltrating lymphocytes (TILs) in invasive breast cancers are assessed solely on the basis of their number, whereas their spatial distribution is rarely investigated. Therefore, we evaluated TILs in 579 patients with invasive breast cancer of no special type (IBC-NST) with a focus...

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Autores principales: Du, Xue, Zhou, Zhe, Shao, Yun, Qian, Kun, Wu, Yongfang, Zhang, Jun, Cui, Miao, Wang, Jingjing, Wang, Shengqi, Tai, Yanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885796/
https://www.ncbi.nlm.nih.gov/pubmed/35228530
http://dx.doi.org/10.1038/s41523-022-00389-y
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author Du, Xue
Zhou, Zhe
Shao, Yun
Qian, Kun
Wu, Yongfang
Zhang, Jun
Cui, Miao
Wang, Jingjing
Wang, Shengqi
Tai, Yanhong
author_facet Du, Xue
Zhou, Zhe
Shao, Yun
Qian, Kun
Wu, Yongfang
Zhang, Jun
Cui, Miao
Wang, Jingjing
Wang, Shengqi
Tai, Yanhong
author_sort Du, Xue
collection PubMed
description Currently, tumor-infiltrating lymphocytes (TILs) in invasive breast cancers are assessed solely on the basis of their number, whereas their spatial distribution is rarely investigated. Therefore, we evaluated TILs in 579 patients with invasive breast cancer of no special type (IBC-NST) with a focus on their spatial distributions in tumor center (TC) and invasive margin (IM). We also assessed a new factor, namely para-tumor infiltrating lymphocytes (PILs) in the para-tumor lobular area (Para). Five immunoarchitectural patterns (IPs) were observed, which were significantly associated with clinicopathological features, especially molecular subtypes, histological grades, clinical stages, and programmed death-ligand 1 (PD-L1) expression. High-TIL density (IP1/2) correlated with favorable disease-free survival (DFS) in TNBC patients (p = 0.04), but opposite results were observed for luminal B subtype patients (both the lowest TIL and PIL densities (IP5) correlated with good DFS, p = 0.013). Luminal B patients with high TILs in the IM and low TILs in the TC (IP3) exhibited the worst DFS, whereas those with low TILs (similar to IP5) and high PILs (IP4) exhibited poor DFS. We also identified TIL subpopulations with significantly different IPs. Our findings suggest that IP can be a potential prognostic factor for tumor immunity in IBC.
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spelling pubmed-88857962022-03-17 Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer Du, Xue Zhou, Zhe Shao, Yun Qian, Kun Wu, Yongfang Zhang, Jun Cui, Miao Wang, Jingjing Wang, Shengqi Tai, Yanhong NPJ Breast Cancer Article Currently, tumor-infiltrating lymphocytes (TILs) in invasive breast cancers are assessed solely on the basis of their number, whereas their spatial distribution is rarely investigated. Therefore, we evaluated TILs in 579 patients with invasive breast cancer of no special type (IBC-NST) with a focus on their spatial distributions in tumor center (TC) and invasive margin (IM). We also assessed a new factor, namely para-tumor infiltrating lymphocytes (PILs) in the para-tumor lobular area (Para). Five immunoarchitectural patterns (IPs) were observed, which were significantly associated with clinicopathological features, especially molecular subtypes, histological grades, clinical stages, and programmed death-ligand 1 (PD-L1) expression. High-TIL density (IP1/2) correlated with favorable disease-free survival (DFS) in TNBC patients (p = 0.04), but opposite results were observed for luminal B subtype patients (both the lowest TIL and PIL densities (IP5) correlated with good DFS, p = 0.013). Luminal B patients with high TILs in the IM and low TILs in the TC (IP3) exhibited the worst DFS, whereas those with low TILs (similar to IP5) and high PILs (IP4) exhibited poor DFS. We also identified TIL subpopulations with significantly different IPs. Our findings suggest that IP can be a potential prognostic factor for tumor immunity in IBC. Nature Publishing Group UK 2022-02-28 /pmc/articles/PMC8885796/ /pubmed/35228530 http://dx.doi.org/10.1038/s41523-022-00389-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Du, Xue
Zhou, Zhe
Shao, Yun
Qian, Kun
Wu, Yongfang
Zhang, Jun
Cui, Miao
Wang, Jingjing
Wang, Shengqi
Tai, Yanhong
Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title_full Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title_fullStr Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title_full_unstemmed Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title_short Immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
title_sort immunoarchitectural patterns as potential prognostic factors for invasive ductal breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885796/
https://www.ncbi.nlm.nih.gov/pubmed/35228530
http://dx.doi.org/10.1038/s41523-022-00389-y
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