Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study

Purpose: The purpose was to evaluate the activity and toxicity of split-dose paclitaxel or docetaxel in combination with gemcitabine in patients with metastatic breast cancer (MBC) who had previously received anthracyclines. Patients and methods: A total of 210 patients were randomly assigned to one...

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Main Authors: Kei Siong Khoo, Syed Hasan Manzoor Zaidi, Vichien Srimuninnimit, Santai Song, Reena Nair, Corazon A. Ngelangel, Anita Bustam, William H.H. Reece, Manfred Lehnert
Other Authors: National Cancer Centre, Singapore
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/23004
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spelling th-mahidol.230042018-08-20T14:14:15Z Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study Kei Siong Khoo Syed Hasan Manzoor Zaidi Vichien Srimuninnimit Santai Song Reena Nair Corazon A. Ngelangel Anita Bustam William H.H. Reece Manfred Lehnert National Cancer Centre, Singapore Baquai Institute of Oncology Mahidol University 307 Hospital of PLA Tata Memorial Hospital Philippine General Hospital University of Malaya Medical Centre Clinical Outcomes and Research Institute Eli Lilly Asian Operations Biochemistry, Genetics and Molecular Biology Medicine Purpose: The purpose was to evaluate the activity and toxicity of split-dose paclitaxel or docetaxel in combination with gemcitabine in patients with metastatic breast cancer (MBC) who had previously received anthracyclines. Patients and methods: A total of 210 patients were randomly assigned to one of three treatment arms: gemcitabine 1250 mg/m2Days 1 and 8 and paclitaxel 175 mg/m2as a 3-h infusion on Day 1 (GP1); gemcitabine 1000 mg/m2Days 1 and 8 and paclitaxel 100 mg/m2as a 1-h infusion on Days 1 and 8 (GP2); gemcitabine 1000 mg/m2Days 1 and 8 and docetaxel 40 mg/m2as a 1-h infusion on Days 1 and 8 (GD). Cycles were repeated every 3 weeks. Results: For the 204 patients evaluable for response assessment, the response rates were 48.6% for GP1, 52.2% for GP2, and 52.3% for GD. Median response duration, time to treatment failure, and time to progression (TTP) were similar in each arm. Median TTP for GP1, GP2 and GD was 7.5, 7.0 and 7.4 months, respectively. For the 208 patients evaluable for safety, the most common grade 3/4 toxicity for each regimen was neutropaenia, with 64%, 57%, and 68% for GP1, GP2, and GD, respectively. Grade 4 neutropaenia, grade 3/4 anaemia, febrile neutropaenia, and diarrhoea were more common in the docetaxel arm, as was the use of intravenous antibiotics and blood transfusions. Conclusion: The study confirmed the high activity of gemcitabine-taxane combinations in MBC. Split-dose paclitaxel had similar activity and toxicity to the 3-weekly administration. The split-dose docetaxel regimen had similar activity to the paclitaxel combinations though associated with higher toxicity. © 2006 Elsevier Ltd. All rights reserved. 2018-08-20T06:50:42Z 2018-08-20T06:50:42Z 2006-08-01 Article European Journal of Cancer. Vol.42, No.12 (2006), 1797-1806 10.1016/j.ejca.2006.05.001 09598049 2-s2.0-33746656336 https://repository.li.mahidol.ac.th/handle/123456789/23004 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746656336&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Kei Siong Khoo
Syed Hasan Manzoor Zaidi
Vichien Srimuninnimit
Santai Song
Reena Nair
Corazon A. Ngelangel
Anita Bustam
William H.H. Reece
Manfred Lehnert
Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
description Purpose: The purpose was to evaluate the activity and toxicity of split-dose paclitaxel or docetaxel in combination with gemcitabine in patients with metastatic breast cancer (MBC) who had previously received anthracyclines. Patients and methods: A total of 210 patients were randomly assigned to one of three treatment arms: gemcitabine 1250 mg/m2Days 1 and 8 and paclitaxel 175 mg/m2as a 3-h infusion on Day 1 (GP1); gemcitabine 1000 mg/m2Days 1 and 8 and paclitaxel 100 mg/m2as a 1-h infusion on Days 1 and 8 (GP2); gemcitabine 1000 mg/m2Days 1 and 8 and docetaxel 40 mg/m2as a 1-h infusion on Days 1 and 8 (GD). Cycles were repeated every 3 weeks. Results: For the 204 patients evaluable for response assessment, the response rates were 48.6% for GP1, 52.2% for GP2, and 52.3% for GD. Median response duration, time to treatment failure, and time to progression (TTP) were similar in each arm. Median TTP for GP1, GP2 and GD was 7.5, 7.0 and 7.4 months, respectively. For the 208 patients evaluable for safety, the most common grade 3/4 toxicity for each regimen was neutropaenia, with 64%, 57%, and 68% for GP1, GP2, and GD, respectively. Grade 4 neutropaenia, grade 3/4 anaemia, febrile neutropaenia, and diarrhoea were more common in the docetaxel arm, as was the use of intravenous antibiotics and blood transfusions. Conclusion: The study confirmed the high activity of gemcitabine-taxane combinations in MBC. Split-dose paclitaxel had similar activity and toxicity to the 3-weekly administration. The split-dose docetaxel regimen had similar activity to the paclitaxel combinations though associated with higher toxicity. © 2006 Elsevier Ltd. All rights reserved.
author2 National Cancer Centre, Singapore
author_facet National Cancer Centre, Singapore
Kei Siong Khoo
Syed Hasan Manzoor Zaidi
Vichien Srimuninnimit
Santai Song
Reena Nair
Corazon A. Ngelangel
Anita Bustam
William H.H. Reece
Manfred Lehnert
format Article
author Kei Siong Khoo
Syed Hasan Manzoor Zaidi
Vichien Srimuninnimit
Santai Song
Reena Nair
Corazon A. Ngelangel
Anita Bustam
William H.H. Reece
Manfred Lehnert
author_sort Kei Siong Khoo
title Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
title_short Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
title_full Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
title_fullStr Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
title_full_unstemmed Gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: A randomised phase II study
title_sort gemcitabine and split-dose paclitaxel or docetaxel in metastatic breast cancer: a randomised phase ii study
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/23004
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