Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer

Aim: The combination of a taxane and capecitabine offers synergistic antitumor activity. This study aimed to determine the efficacy and tolerability of a paclitaxel and capecitabine combination in Thai patients with metastatic breast cancer (MBC) not previously treated for metastatic disease. Method...

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Main Authors: Chitapanarux,I., Kamnerdsupaphon,P., Tharavichitkul,E., Lorvidhaya,V., Trakultivakorn,H., Srisukho,S., Somwangprasert,A., Watcharachan,K., Sukthomya,V.
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Published: Wiley-Blackwell 2015
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http://cmuir.cmu.ac.th/handle/6653943832/38197
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-381972015-06-16T07:46:35Z Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer Chitapanarux,I. Kamnerdsupaphon,P. Tharavichitkul,E. Lorvidhaya,V. Trakultivakorn,H. Srisukho,S. Somwangprasert,A. Watcharachan,K. Sukthomya,V. Oncology Aim: The combination of a taxane and capecitabine offers synergistic antitumor activity. This study aimed to determine the efficacy and tolerability of a paclitaxel and capecitabine combination in Thai patients with metastatic breast cancer (MBC) not previously treated for metastatic disease. Methods: This open-label, single-center, non-comparative phase II study was conducted between December 2006 and March 2009. In all 40 MBC patients were treated with oral capecitabine 1000mg/m 2 twice daily on days 1 to 14, and weekly paclitaxel 80mg/m 2 in a 3-week cycle for a total of six cycles. Results: After a median follow up of 13.4 months, an overall objective response rate of 80%, with a partial response of 74% and a complete response of 5% were achieved. While 8% of patients achieved stable disease, 13% had progressive disease. Median time to progress was 8 months and median overall survival was 24.4 months. One patient discontinued because of hypersensitivity to paclitaxel. There was no grade 4 toxicity. Skin and nail toxicity was found in 75% of patients (with 25% in grade 2 or 3), followed by neutropenia (45% in all with 15% in grades 2 or 3), neuropathy (25% in total with 5% in grade 2) and stomatitis and diarrhea (in both of which 5% experienced grade 1 severity). Conclusion: A first-line regimen of weekly paclitaxel plus capecitabine is effective and tolerable in Thai MBC patients. © 2012 Blackwell Publishing Asia Pty Ltd. 2015-06-16T07:46:35Z 2015-06-16T07:46:35Z 2011-03-01 Article 17437555 2-s2.0-84857648437 10.1111/j.1743-7563.2011.01467.x 22369447 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84857648437&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38197 Wiley-Blackwell
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Oncology
spellingShingle Oncology
Chitapanarux,I.
Kamnerdsupaphon,P.
Tharavichitkul,E.
Lorvidhaya,V.
Trakultivakorn,H.
Srisukho,S.
Somwangprasert,A.
Watcharachan,K.
Sukthomya,V.
Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
description Aim: The combination of a taxane and capecitabine offers synergistic antitumor activity. This study aimed to determine the efficacy and tolerability of a paclitaxel and capecitabine combination in Thai patients with metastatic breast cancer (MBC) not previously treated for metastatic disease. Methods: This open-label, single-center, non-comparative phase II study was conducted between December 2006 and March 2009. In all 40 MBC patients were treated with oral capecitabine 1000mg/m 2 twice daily on days 1 to 14, and weekly paclitaxel 80mg/m 2 in a 3-week cycle for a total of six cycles. Results: After a median follow up of 13.4 months, an overall objective response rate of 80%, with a partial response of 74% and a complete response of 5% were achieved. While 8% of patients achieved stable disease, 13% had progressive disease. Median time to progress was 8 months and median overall survival was 24.4 months. One patient discontinued because of hypersensitivity to paclitaxel. There was no grade 4 toxicity. Skin and nail toxicity was found in 75% of patients (with 25% in grade 2 or 3), followed by neutropenia (45% in all with 15% in grades 2 or 3), neuropathy (25% in total with 5% in grade 2) and stomatitis and diarrhea (in both of which 5% experienced grade 1 severity). Conclusion: A first-line regimen of weekly paclitaxel plus capecitabine is effective and tolerable in Thai MBC patients. © 2012 Blackwell Publishing Asia Pty Ltd.
format Article
author Chitapanarux,I.
Kamnerdsupaphon,P.
Tharavichitkul,E.
Lorvidhaya,V.
Trakultivakorn,H.
Srisukho,S.
Somwangprasert,A.
Watcharachan,K.
Sukthomya,V.
author_facet Chitapanarux,I.
Kamnerdsupaphon,P.
Tharavichitkul,E.
Lorvidhaya,V.
Trakultivakorn,H.
Srisukho,S.
Somwangprasert,A.
Watcharachan,K.
Sukthomya,V.
author_sort Chitapanarux,I.
title Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
title_short Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
title_full Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
title_fullStr Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
title_full_unstemmed Capecitabine and weekly paclitaxel as first-line therapy in Thai patients with metastatic breast cancer
title_sort capecitabine and weekly paclitaxel as first-line therapy in thai patients with metastatic breast cancer
publisher Wiley-Blackwell
publishDate 2015
url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84857648437&origin=inward
http://cmuir.cmu.ac.th/handle/6653943832/38197
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