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Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study

Advanced biliary tract carcinomas (BTCs) are often diagnosed at an advanced/metastatic stage and have a poor prognosis. The combination of gemcitabine and oxaliplatin (GEMOX) has shown promising activity in this setting. This international phase II study evaluated the efficacy and safety of GEMOX as...

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Autores principales: André, T, Reyes-Vidal, J M, Fartoux, L, Ross, P, Leslie, M, Rosmorduc, O, Clemens, M R, Louvet, C, Perez, N, Mehmud, F, Scheithauer, W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538748/
https://www.ncbi.nlm.nih.gov/pubmed/19238628
http://dx.doi.org/10.1038/sj.bjc.6604628
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author André, T
Reyes-Vidal, J M
Fartoux, L
Ross, P
Leslie, M
Rosmorduc, O
Clemens, M R
Louvet, C
Perez, N
Mehmud, F
Scheithauer, W
author_facet André, T
Reyes-Vidal, J M
Fartoux, L
Ross, P
Leslie, M
Rosmorduc, O
Clemens, M R
Louvet, C
Perez, N
Mehmud, F
Scheithauer, W
author_sort André, T
collection PubMed
description Advanced biliary tract carcinomas (BTCs) are often diagnosed at an advanced/metastatic stage and have a poor prognosis. The combination of gemcitabine and oxaliplatin (GEMOX) has shown promising activity in this setting. This international phase II study evaluated the efficacy and safety of GEMOX as first-line therapy in patients with advanced BTCs. Eligible patients with previously untreated locally advanced or metastatic BTC received gemcitabine 1000 mg m(−2) (day 1) and oxaliplatin 100 mg m(−2) (day 2), every 2 weeks. Seventy patients were enroled; 72.9% had metastatic disease. Sixty-seven patients were treated. There were 10 confirmed partial responses (14.9%; 95% confidence interval (CI), 7.4–25.7%) in the treated population (RECIST). Twenty-four patients (35.8 %) had stable disease. The objective response rate was 20.5% in patients with non-gallbladder cancers (9/44 patients) and 4.3% in patients with gallbladder cancers (1/23). Median overall survival for the intent-to-treat population was 8.8 months (95% CI, 6.9–11.1%) and progression-free survival was 3.4 months (95% CI, 2.5–4.6%). Grade 3/4 toxicities included thrombocytopenia (14.9% of patients), alanine aminotransferase elevation (13.4%), anaemia (10.4%), neutropenia (11.9%) and pain (11.9%). In this study, GEMOX demonstrated activity in non-gallbladder carcinoma, but poor activity in gallbladder carcinoma. GEMOX is well tolerated in advanced BTCs.
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spelling pubmed-25387482009-09-16 Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study André, T Reyes-Vidal, J M Fartoux, L Ross, P Leslie, M Rosmorduc, O Clemens, M R Louvet, C Perez, N Mehmud, F Scheithauer, W Br J Cancer Clinical Study Advanced biliary tract carcinomas (BTCs) are often diagnosed at an advanced/metastatic stage and have a poor prognosis. The combination of gemcitabine and oxaliplatin (GEMOX) has shown promising activity in this setting. This international phase II study evaluated the efficacy and safety of GEMOX as first-line therapy in patients with advanced BTCs. Eligible patients with previously untreated locally advanced or metastatic BTC received gemcitabine 1000 mg m(−2) (day 1) and oxaliplatin 100 mg m(−2) (day 2), every 2 weeks. Seventy patients were enroled; 72.9% had metastatic disease. Sixty-seven patients were treated. There were 10 confirmed partial responses (14.9%; 95% confidence interval (CI), 7.4–25.7%) in the treated population (RECIST). Twenty-four patients (35.8 %) had stable disease. The objective response rate was 20.5% in patients with non-gallbladder cancers (9/44 patients) and 4.3% in patients with gallbladder cancers (1/23). Median overall survival for the intent-to-treat population was 8.8 months (95% CI, 6.9–11.1%) and progression-free survival was 3.4 months (95% CI, 2.5–4.6%). Grade 3/4 toxicities included thrombocytopenia (14.9% of patients), alanine aminotransferase elevation (13.4%), anaemia (10.4%), neutropenia (11.9%) and pain (11.9%). In this study, GEMOX demonstrated activity in non-gallbladder carcinoma, but poor activity in gallbladder carcinoma. GEMOX is well tolerated in advanced BTCs. Nature Publishing Group 2008-09-16 2008-08-26 /pmc/articles/PMC2538748/ /pubmed/19238628 http://dx.doi.org/10.1038/sj.bjc.6604628 Text en Copyright © 2008 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
André, T
Reyes-Vidal, J M
Fartoux, L
Ross, P
Leslie, M
Rosmorduc, O
Clemens, M R
Louvet, C
Perez, N
Mehmud, F
Scheithauer, W
Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title_full Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title_fullStr Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title_full_unstemmed Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title_short Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study
title_sort gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase ii study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538748/
https://www.ncbi.nlm.nih.gov/pubmed/19238628
http://dx.doi.org/10.1038/sj.bjc.6604628
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