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Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer

PURPOSE: The objective of this research was to compare the short- and long-term efficacy of the following four neoadjuvant chemotherapy (NAC) regimens: docetaxel/carboplatin/trastuzumab (TCH), docetaxel/epirubicin/cyclophosphamide (TEC), Xeloda/epirubicin/cyclophosphamide followed by Xeloda/docetaxe...

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Autores principales: Li, Si, Wei, Wei, Jiang, Yi, Li, Qiuyun, Huang, Qinghua, Yang, Huawei, Liu, Jianlun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157574/
https://www.ncbi.nlm.nih.gov/pubmed/30275685
http://dx.doi.org/10.2147/DDDT.S171534
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author Li, Si
Wei, Wei
Jiang, Yi
Li, Qiuyun
Huang, Qinghua
Yang, Huawei
Liu, Jianlun
author_facet Li, Si
Wei, Wei
Jiang, Yi
Li, Qiuyun
Huang, Qinghua
Yang, Huawei
Liu, Jianlun
author_sort Li, Si
collection PubMed
description PURPOSE: The objective of this research was to compare the short- and long-term efficacy of the following four neoadjuvant chemotherapy (NAC) regimens: docetaxel/carboplatin/trastuzumab (TCH), docetaxel/epirubicin/cyclophosphamide (TEC), Xeloda/epirubicin/cyclophosphamide followed by Xeloda/docetaxel (XEC-XT), and 5-fluorouracil/epirubicin/cyclophosphamide followed by docetaxel (FEC-T) in human epidermal growth factor receptor-2-positive (Her-2-positive) breast cancer. PATIENTS AND METHODS: According to treatment preferences, 139 patients with Her-2-positive breast cancer were divided into the following four groups: 39 patients in the TCH group, 35 patients in the TEC group, 33 patients in the XEC-XT group, and 32 patients in the FEC-T group. The primary end points were disease-free survival (DFS) and 5-year overall survival (5-year OS). The secondary end points were the efficacy and toxicity of NAC. RESULTS: The TCH, TEC, XEC-XT, and FEC-T groups demonstrated overall response rates of 87.1%, 74.3%, 75.8%, and 62.5% (P=0.031), respectively, and pathological complete response rates of 25.6%, 18.2%, 20.0%, and 18.2% (P=0.041), respectively. The DFS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 84.6%, 62.9%, 65.7%, and 46.9% (P=0.01), respectively. The 5-year OS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 87.2%, 69.7%, 71.4%, and 59.4% (P=0.069), respectively. The mean survival time was 59.3 months (TCH group), 53.5 months (TEC group), 55.3 months (XEC-XT group), and 52.4 months (FEC-T group). The difference in survival among the four groups was statistically significant (P=0.04). CONCLUSION: In four NAC regimens for the treatment of Her-2-positive breast cancer, the TCH group exhibited better DFS and 5-year OS. The TCH regimen significantly enhanced the pathological complete remission rate of NAC with similar side effects compared to the TEC, XEC-XT, and FEC-T regimens. In terms of long-term efficacy, the XEC-XT treatment was superior to the FEC-T and TEC treatment, and there was no significant difference between the FEC-T and TEC groups.
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spelling pubmed-61575742018-10-01 Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer Li, Si Wei, Wei Jiang, Yi Li, Qiuyun Huang, Qinghua Yang, Huawei Liu, Jianlun Drug Des Devel Ther Original Research PURPOSE: The objective of this research was to compare the short- and long-term efficacy of the following four neoadjuvant chemotherapy (NAC) regimens: docetaxel/carboplatin/trastuzumab (TCH), docetaxel/epirubicin/cyclophosphamide (TEC), Xeloda/epirubicin/cyclophosphamide followed by Xeloda/docetaxel (XEC-XT), and 5-fluorouracil/epirubicin/cyclophosphamide followed by docetaxel (FEC-T) in human epidermal growth factor receptor-2-positive (Her-2-positive) breast cancer. PATIENTS AND METHODS: According to treatment preferences, 139 patients with Her-2-positive breast cancer were divided into the following four groups: 39 patients in the TCH group, 35 patients in the TEC group, 33 patients in the XEC-XT group, and 32 patients in the FEC-T group. The primary end points were disease-free survival (DFS) and 5-year overall survival (5-year OS). The secondary end points were the efficacy and toxicity of NAC. RESULTS: The TCH, TEC, XEC-XT, and FEC-T groups demonstrated overall response rates of 87.1%, 74.3%, 75.8%, and 62.5% (P=0.031), respectively, and pathological complete response rates of 25.6%, 18.2%, 20.0%, and 18.2% (P=0.041), respectively. The DFS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 84.6%, 62.9%, 65.7%, and 46.9% (P=0.01), respectively. The 5-year OS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 87.2%, 69.7%, 71.4%, and 59.4% (P=0.069), respectively. The mean survival time was 59.3 months (TCH group), 53.5 months (TEC group), 55.3 months (XEC-XT group), and 52.4 months (FEC-T group). The difference in survival among the four groups was statistically significant (P=0.04). CONCLUSION: In four NAC regimens for the treatment of Her-2-positive breast cancer, the TCH group exhibited better DFS and 5-year OS. The TCH regimen significantly enhanced the pathological complete remission rate of NAC with similar side effects compared to the TEC, XEC-XT, and FEC-T regimens. In terms of long-term efficacy, the XEC-XT treatment was superior to the FEC-T and TEC treatment, and there was no significant difference between the FEC-T and TEC groups. Dove Medical Press 2018-09-21 /pmc/articles/PMC6157574/ /pubmed/30275685 http://dx.doi.org/10.2147/DDDT.S171534 Text en © 2018 Li et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Li, Si
Wei, Wei
Jiang, Yi
Li, Qiuyun
Huang, Qinghua
Yang, Huawei
Liu, Jianlun
Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title_full Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title_fullStr Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title_full_unstemmed Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title_short Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer
title_sort comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for her-2-positive breast cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157574/
https://www.ncbi.nlm.nih.gov/pubmed/30275685
http://dx.doi.org/10.2147/DDDT.S171534
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