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Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer
We conducted this study to ascertain the efficacy and toxicity of docetaxel and cisplatin combined with oral UFT and leucovorin as a first-line treatment for patients with advanced gastric cancer. In all, 52 patients received courses of docetaxel 60 mg m(−2) intravenously (i.v.) for 1 h and then cis...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361894/ https://www.ncbi.nlm.nih.gov/pubmed/15726097 http://dx.doi.org/10.1038/sj.bjc.6602446 |
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author | Oh, S C Park, K H Choi, I K Yoon, S Y Kim, S J Seo, J H Choi, C W Kim, B S Shin, S W Kim, J S Kim, Y H |
author_facet | Oh, S C Park, K H Choi, I K Yoon, S Y Kim, S J Seo, J H Choi, C W Kim, B S Shin, S W Kim, J S Kim, Y H |
author_sort | Oh, S C |
collection | PubMed |
description | We conducted this study to ascertain the efficacy and toxicity of docetaxel and cisplatin combined with oral UFT and leucovorin as a first-line treatment for patients with advanced gastric cancer. In all, 52 patients received courses of docetaxel 60 mg m(−2) intravenously (i.v.) for 1 h and then cisplatin 75 mg m(−2) i.v. for 2 h on day 1. Oral UFT at 400–600 mg day(−1), as determined by body surface area, and leucovorin at 75 mg day(−1) were administered for 21 consecutive days from day 1, and this was followed by a 7-day drug-free interval. A total of 225 courses were administered, and the median number of courses per patient was four. Four complete responses (7.7%) and 22 partial responses (42.3%) were achieved, giving an overall response rate of 50% (95% Confidence Interval: 36.4–63.6%). The major toxicity was neutropenia, which reached grade 3/4 in 36 patients (69.3%). Grade 3/4 nausea and vomiting was observed in 12 patients (23.1%). Median time to progression was 22 weeks (4 to 156+ weeks), median survival duration was 48 weeks (4 to 156+ weeks), and median response duration was 24 weeks (6–152 weeks). We conclude that docetaxel, cisplatin, oral UFT, and leucovorin combination chemotherapy is effective and tolerable for the treatment of advanced gastric cancer. |
format | Text |
id | pubmed-2361894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23618942009-09-10 Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer Oh, S C Park, K H Choi, I K Yoon, S Y Kim, S J Seo, J H Choi, C W Kim, B S Shin, S W Kim, J S Kim, Y H Br J Cancer Clinical Study We conducted this study to ascertain the efficacy and toxicity of docetaxel and cisplatin combined with oral UFT and leucovorin as a first-line treatment for patients with advanced gastric cancer. In all, 52 patients received courses of docetaxel 60 mg m(−2) intravenously (i.v.) for 1 h and then cisplatin 75 mg m(−2) i.v. for 2 h on day 1. Oral UFT at 400–600 mg day(−1), as determined by body surface area, and leucovorin at 75 mg day(−1) were administered for 21 consecutive days from day 1, and this was followed by a 7-day drug-free interval. A total of 225 courses were administered, and the median number of courses per patient was four. Four complete responses (7.7%) and 22 partial responses (42.3%) were achieved, giving an overall response rate of 50% (95% Confidence Interval: 36.4–63.6%). The major toxicity was neutropenia, which reached grade 3/4 in 36 patients (69.3%). Grade 3/4 nausea and vomiting was observed in 12 patients (23.1%). Median time to progression was 22 weeks (4 to 156+ weeks), median survival duration was 48 weeks (4 to 156+ weeks), and median response duration was 24 weeks (6–152 weeks). We conclude that docetaxel, cisplatin, oral UFT, and leucovorin combination chemotherapy is effective and tolerable for the treatment of advanced gastric cancer. Nature Publishing Group 2005-03-14 2005-02-22 /pmc/articles/PMC2361894/ /pubmed/15726097 http://dx.doi.org/10.1038/sj.bjc.6602446 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Oh, S C Park, K H Choi, I K Yoon, S Y Kim, S J Seo, J H Choi, C W Kim, B S Shin, S W Kim, J S Kim, Y H Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title | Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title_full | Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title_fullStr | Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title_full_unstemmed | Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title_short | Docetaxel (Taxotere), cisplatin, UFT, and leucovorin combination chemotherapy in advanced gastric cancer |
title_sort | docetaxel (taxotere), cisplatin, uft, and leucovorin combination chemotherapy in advanced gastric cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361894/ https://www.ncbi.nlm.nih.gov/pubmed/15726097 http://dx.doi.org/10.1038/sj.bjc.6602446 |
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