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Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer

BACKGROUND: Whether a sequential or concurrent regimen of anthracyclines and taxanes is superior for breast cancer is controversial. We compared the efficacy of two regimens in patients with operable breast cancer based on all relevant published data of phase III randomized controlled trials. METHOD...

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Autores principales: Chen, Wanjing, Tu, Qian, Shen, Yanfei, Tang, Kejun, Hong, Mengying, Shen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890894/
https://www.ncbi.nlm.nih.gov/pubmed/33602236
http://dx.doi.org/10.1186/s12957-021-02150-4
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author Chen, Wanjing
Tu, Qian
Shen, Yanfei
Tang, Kejun
Hong, Mengying
Shen, Yong
author_facet Chen, Wanjing
Tu, Qian
Shen, Yanfei
Tang, Kejun
Hong, Mengying
Shen, Yong
author_sort Chen, Wanjing
collection PubMed
description BACKGROUND: Whether a sequential or concurrent regimen of anthracyclines and taxanes is superior for breast cancer is controversial. We compared the efficacy of two regimens in patients with operable breast cancer based on all relevant published data of phase III randomized controlled trials. METHODS: A comprehensive literature search on PubMed, Web of Science, Embase, ScienceDirect, Google Scholar, and ClinicalTrials.gov databases was performed up to May 2020. Meta-analysis was performed to evaluate the different efficacy on disease-free survival (DFS) and overall survival (OS) for the two chemotherapy regimens. Subgroup analyses were further carried out in terms of node status and anthracycline selection. RESULTS: Compared to the concurrent regimen, the sequential regimen did not improve the DFS or OS in the population studied. Subgroup analysis showed that in node-positive patients, the sequential regimen had better DFS, but not OS, than the concurrent regimen. In sequential regimen, patients who received doxorubicin and taxanes had improved DFS and OS than patients who were administered epirubicin and taxanes. Furthermore, for patients who received doxorubicin and taxanes, compared to the sequential regimen, fewer cycles (4 cycles) of concurrent treatment resulted in a worse DFS and OS, which can be rescued by more cycles (6 cycles). CONCLUSIONS: The sequential regimen of anthracyclines and taxanes for patients with operable breast cancer did not yield a significant benefit in DFS or OS over the concurrent regimen. The sequential regimen, however, provided a better DFS than concurrent regimen for node-positive patients. Interestingly, further subgroup analysis showed that for node-positive patients who were given doxorubicin and taxanes, more cycles (6 cycles) of the concurrent regimen may rescue the efficacy for fewer cycles (4 cycles).
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spelling pubmed-78908942021-02-22 Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer Chen, Wanjing Tu, Qian Shen, Yanfei Tang, Kejun Hong, Mengying Shen, Yong World J Surg Oncol Research BACKGROUND: Whether a sequential or concurrent regimen of anthracyclines and taxanes is superior for breast cancer is controversial. We compared the efficacy of two regimens in patients with operable breast cancer based on all relevant published data of phase III randomized controlled trials. METHODS: A comprehensive literature search on PubMed, Web of Science, Embase, ScienceDirect, Google Scholar, and ClinicalTrials.gov databases was performed up to May 2020. Meta-analysis was performed to evaluate the different efficacy on disease-free survival (DFS) and overall survival (OS) for the two chemotherapy regimens. Subgroup analyses were further carried out in terms of node status and anthracycline selection. RESULTS: Compared to the concurrent regimen, the sequential regimen did not improve the DFS or OS in the population studied. Subgroup analysis showed that in node-positive patients, the sequential regimen had better DFS, but not OS, than the concurrent regimen. In sequential regimen, patients who received doxorubicin and taxanes had improved DFS and OS than patients who were administered epirubicin and taxanes. Furthermore, for patients who received doxorubicin and taxanes, compared to the sequential regimen, fewer cycles (4 cycles) of concurrent treatment resulted in a worse DFS and OS, which can be rescued by more cycles (6 cycles). CONCLUSIONS: The sequential regimen of anthracyclines and taxanes for patients with operable breast cancer did not yield a significant benefit in DFS or OS over the concurrent regimen. The sequential regimen, however, provided a better DFS than concurrent regimen for node-positive patients. Interestingly, further subgroup analysis showed that for node-positive patients who were given doxorubicin and taxanes, more cycles (6 cycles) of the concurrent regimen may rescue the efficacy for fewer cycles (4 cycles). BioMed Central 2021-02-18 /pmc/articles/PMC7890894/ /pubmed/33602236 http://dx.doi.org/10.1186/s12957-021-02150-4 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Wanjing
Tu, Qian
Shen, Yanfei
Tang, Kejun
Hong, Mengying
Shen, Yong
Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title_full Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title_fullStr Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title_full_unstemmed Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title_short Sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
title_sort sequential vs concurrent adjuvant chemotherapy of anthracycline and taxane for operable breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890894/
https://www.ncbi.nlm.nih.gov/pubmed/33602236
http://dx.doi.org/10.1186/s12957-021-02150-4
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