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Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab

PURPOSE: The tumor-infiltrating lymphocytes (TILs) expression in breast cancer is a positive prognostic marker for certain breast cancer subtypes. We evaluated the efficacy of dual anti-human epidermal growth factor receptor 2 (HER2) blockade in HER2-positive breast cancer and hypothesized that high...

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Autores principales: Ha, Joo Young, Kim, Jeong Eun, Lee, Hee Jin, Jeong, Jae Ho, Ahn, Jin-Hee, Jung, Kyung Hae, Gong, Gyungyub, Chae, Eun Young, Kim, Hak Hee, Chung, Il Yong, Ko, Beom Seok, Kim, Sung-Bae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Breast Cancer Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410619/
https://www.ncbi.nlm.nih.gov/pubmed/34352937
http://dx.doi.org/10.4048/jbc.2021.24.e36
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author Ha, Joo Young
Kim, Jeong Eun
Lee, Hee Jin
Jeong, Jae Ho
Ahn, Jin-Hee
Jung, Kyung Hae
Gong, Gyungyub
Chae, Eun Young
Kim, Hak Hee
Chung, Il Yong
Ko, Beom Seok
Kim, Sung-Bae
author_facet Ha, Joo Young
Kim, Jeong Eun
Lee, Hee Jin
Jeong, Jae Ho
Ahn, Jin-Hee
Jung, Kyung Hae
Gong, Gyungyub
Chae, Eun Young
Kim, Hak Hee
Chung, Il Yong
Ko, Beom Seok
Kim, Sung-Bae
author_sort Ha, Joo Young
collection PubMed
description PURPOSE: The tumor-infiltrating lymphocytes (TILs) expression in breast cancer is a positive prognostic marker for certain breast cancer subtypes. We evaluated the efficacy of dual anti-human epidermal growth factor receptor 2 (HER2) blockade in HER2-positive breast cancer and hypothesized that high TILs tumors are associated with better outcomes. METHODS: A total of 176 patients who were treated with neoadjuvant docetaxel, carboplatin, trastuzumab, and pertuzumab (TCHP) between December 2015 and December 2018 were reviewed. They were grouped based on a cut-off value of the stromal TILs grade (≤ 20% TILs, > 20% TILs). RESULTS: In total, 107 patients (60.8%) achieved pathological complete response (pCR). Hormone receptor (HR)-negativity (p = 0.001) and a high TILs grade (p = 0.022) were independent predictors of pCR. Among the HR-negative patients, high TILs tumors were significantly associated with pCR (p = 0.035). CONCLUSION: HR status and the TILs grade are significantly correlated with pCR in dual anti-HER2 neoadjuvant therapy. The evaluation of the TILs at baseline may be beneficial for predicting pCR in HER2-positive breast cancer.
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spelling pubmed-84106192021-09-08 Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab Ha, Joo Young Kim, Jeong Eun Lee, Hee Jin Jeong, Jae Ho Ahn, Jin-Hee Jung, Kyung Hae Gong, Gyungyub Chae, Eun Young Kim, Hak Hee Chung, Il Yong Ko, Beom Seok Kim, Sung-Bae J Breast Cancer Original Article PURPOSE: The tumor-infiltrating lymphocytes (TILs) expression in breast cancer is a positive prognostic marker for certain breast cancer subtypes. We evaluated the efficacy of dual anti-human epidermal growth factor receptor 2 (HER2) blockade in HER2-positive breast cancer and hypothesized that high TILs tumors are associated with better outcomes. METHODS: A total of 176 patients who were treated with neoadjuvant docetaxel, carboplatin, trastuzumab, and pertuzumab (TCHP) between December 2015 and December 2018 were reviewed. They were grouped based on a cut-off value of the stromal TILs grade (≤ 20% TILs, > 20% TILs). RESULTS: In total, 107 patients (60.8%) achieved pathological complete response (pCR). Hormone receptor (HR)-negativity (p = 0.001) and a high TILs grade (p = 0.022) were independent predictors of pCR. Among the HR-negative patients, high TILs tumors were significantly associated with pCR (p = 0.035). CONCLUSION: HR status and the TILs grade are significantly correlated with pCR in dual anti-HER2 neoadjuvant therapy. The evaluation of the TILs at baseline may be beneficial for predicting pCR in HER2-positive breast cancer. Korean Breast Cancer Society 2021-07-09 /pmc/articles/PMC8410619/ /pubmed/34352937 http://dx.doi.org/10.4048/jbc.2021.24.e36 Text en © 2021 Korean Breast Cancer Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ha, Joo Young
Kim, Jeong Eun
Lee, Hee Jin
Jeong, Jae Ho
Ahn, Jin-Hee
Jung, Kyung Hae
Gong, Gyungyub
Chae, Eun Young
Kim, Hak Hee
Chung, Il Yong
Ko, Beom Seok
Kim, Sung-Bae
Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title_full Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title_fullStr Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title_full_unstemmed Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title_short Tumor-Infiltrating Lymphocytes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Receiving Neoadjuvant Docetaxel, Carboplatin, Trastuzumab, and Pertuzumab
title_sort tumor-infiltrating lymphocytes in human epidermal growth factor receptor 2-positive breast cancer receiving neoadjuvant docetaxel, carboplatin, trastuzumab, and pertuzumab
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410619/
https://www.ncbi.nlm.nih.gov/pubmed/34352937
http://dx.doi.org/10.4048/jbc.2021.24.e36
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