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Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer

Our objective was to investigate the efficacy and safety of capecitabine maintenance therapy (CMT) after capecitabine-based combination chemotherapy in patients with metastatic breast cancer. The clinical data of 139 metastatic breast cancer patients treated from March 2008 to May 2012 with capecita...

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Autores principales: Si, W., Zhu, Y.Y., Li, Y., Gao, P., Han, C., You, J.H., Linghu, R.X., Jiao, S.C., Yang, J.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935280/
https://www.ncbi.nlm.nih.gov/pubmed/24345917
http://dx.doi.org/10.1590/1414-431X20133168
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author Si, W.
Zhu, Y.Y.
Li, Y.
Gao, P.
Han, C.
You, J.H.
Linghu, R.X.
Jiao, S.C.
Yang, J.L.
author_facet Si, W.
Zhu, Y.Y.
Li, Y.
Gao, P.
Han, C.
You, J.H.
Linghu, R.X.
Jiao, S.C.
Yang, J.L.
author_sort Si, W.
collection PubMed
description Our objective was to investigate the efficacy and safety of capecitabine maintenance therapy (CMT) after capecitabine-based combination chemotherapy in patients with metastatic breast cancer. The clinical data of 139 metastatic breast cancer patients treated from March 2008 to May 2012 with capecitabine-based combination chemotherapy were retrospectively analyzed. When initial disease control was achieved by the combination chemotherapy, we used CMT for 50 patients, while 37 patients were treated with a different (non-CMT) maintenance therapy. We compared time to progression (TTP), objective response rate, disease control rate, clinical benefit rate, and safety of the two groups, and a sub-group analysis was performed according to pathological characteristics. Sixty-four percent of the patients received a median of six cycles of a docetaxel+capecitabine combination chemotherapy regimen (range 1-45); the median TTP (MTTP) for the complete treatment was 9.43 months (95%CI=8.38-10.48 months) for the CMT group and 4.5 months (95%CI=4.22-4.78 months; P=0.004) for the non-CMT group. The MTTPs for the maintenance therapies administered after the initial capecitabine combined chemotherapy were 4.11 months (95%CI=3.34-4.87 months) for the CMT group and 2.0 months (95%CI=1.63-2.38 months) for the non-CMT group. Gastrointestinal side effects, decreased white blood cells and palmar-plantar erythrodysesthesia were the main adverse reactions experienced with the combination chemotherapies, CMT and non-CMT treatments. No significant differences in the incidence of adverse reactions were detected in the CMT and non-CMT patients. After initial disease control was achieved with the capecitabine-based combination chemotherapy, CMT can significantly prolong TTP rates with a favorable safety profile.
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spelling pubmed-39352802014-03-07 Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer Si, W. Zhu, Y.Y. Li, Y. Gao, P. Han, C. You, J.H. Linghu, R.X. Jiao, S.C. Yang, J.L. Braz J Med Biol Res Clinical Investigation Our objective was to investigate the efficacy and safety of capecitabine maintenance therapy (CMT) after capecitabine-based combination chemotherapy in patients with metastatic breast cancer. The clinical data of 139 metastatic breast cancer patients treated from March 2008 to May 2012 with capecitabine-based combination chemotherapy were retrospectively analyzed. When initial disease control was achieved by the combination chemotherapy, we used CMT for 50 patients, while 37 patients were treated with a different (non-CMT) maintenance therapy. We compared time to progression (TTP), objective response rate, disease control rate, clinical benefit rate, and safety of the two groups, and a sub-group analysis was performed according to pathological characteristics. Sixty-four percent of the patients received a median of six cycles of a docetaxel+capecitabine combination chemotherapy regimen (range 1-45); the median TTP (MTTP) for the complete treatment was 9.43 months (95%CI=8.38-10.48 months) for the CMT group and 4.5 months (95%CI=4.22-4.78 months; P=0.004) for the non-CMT group. The MTTPs for the maintenance therapies administered after the initial capecitabine combined chemotherapy were 4.11 months (95%CI=3.34-4.87 months) for the CMT group and 2.0 months (95%CI=1.63-2.38 months) for the non-CMT group. Gastrointestinal side effects, decreased white blood cells and palmar-plantar erythrodysesthesia were the main adverse reactions experienced with the combination chemotherapies, CMT and non-CMT treatments. No significant differences in the incidence of adverse reactions were detected in the CMT and non-CMT patients. After initial disease control was achieved with the capecitabine-based combination chemotherapy, CMT can significantly prolong TTP rates with a favorable safety profile. Associação Brasileira de Divulgação Científica 2013-11-25 /pmc/articles/PMC3935280/ /pubmed/24345917 http://dx.doi.org/10.1590/1414-431X20133168 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Si, W.
Zhu, Y.Y.
Li, Y.
Gao, P.
Han, C.
You, J.H.
Linghu, R.X.
Jiao, S.C.
Yang, J.L.
Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title_full Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title_fullStr Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title_full_unstemmed Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title_short Capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
title_sort capecitabine maintenance therapy in patients with recurrent or metastatic breast cancer
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935280/
https://www.ncbi.nlm.nih.gov/pubmed/24345917
http://dx.doi.org/10.1590/1414-431X20133168
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