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Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study

BACKGROUND: 5-fluorouracil remains the standard therapy for patients with advanced/metastatic colorectal cancer. Pre-clinical studies have demonstrated the biological modulation of 5-fluorouracil by methotrexate and leucovorin. This phase II study was initiated to determine the activity and toxicity...

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Autores principales: Tomlinson, Shannon K, Melin, Susan A, Higgs, Vetta, White, Douglas R, Savage, Paul, Case, Douglas, Blackstock, A William
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC113263/
https://www.ncbi.nlm.nih.gov/pubmed/11988109
http://dx.doi.org/10.1186/1471-2407-2-9
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author Tomlinson, Shannon K
Melin, Susan A
Higgs, Vetta
White, Douglas R
Savage, Paul
Case, Douglas
Blackstock, A William
author_facet Tomlinson, Shannon K
Melin, Susan A
Higgs, Vetta
White, Douglas R
Savage, Paul
Case, Douglas
Blackstock, A William
author_sort Tomlinson, Shannon K
collection PubMed
description BACKGROUND: 5-fluorouracil remains the standard therapy for patients with advanced/metastatic colorectal cancer. Pre-clinical studies have demonstrated the biological modulation of 5-fluorouracil by methotrexate and leucovorin. This phase II study was initiated to determine the activity and toxicity of sequential methotrexate – leucovorin and 5-fluorouracil chemotherapy in patients with advanced colorectal cancer. METHODS: Ninety-seven patients with metastatic colorectal cancer were enrolled onto the study. Methotrexate – 30 mg/m(2) was administered every 6 hours for 6 doses followed by a 2 hour infusion of LV – 500 mg/m(2). Midway through the leucovorin infusion, patients received 5-fluorouracil – 600 mg/m(2). This constituted a cycle of therapy and was repeated every 2 weeks until progression. RESULTS: The median age was 64 yrs (34–84) and the Eastern Cooperative Group Oncology performance score was 0 in 37%, 1 in 55% and 2 in 8% of patients. Partial and complete responses were seen in 31% of patients with a median duration of response of 6.4 months. The overall median survival was 13.0 months. The estimated 1-year survival was 53.7%. Grade III and IV toxic effects were modest and included mucositis, nausea and vomiting. CONCLUSIONS: This phase II study supports previously reported data demonstrating the modest clinical benefit of 5-FU modulation utilizing methotrexate and leucovorin in patients with metastatic colorectal cancer. Ongoing studies evaluating 5-fluorouracil modulation with more novel agents (Irinotecan and/or oxaliplatin) are in progress and may prove encouraging.
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spelling pubmed-1132632002-05-23 Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study Tomlinson, Shannon K Melin, Susan A Higgs, Vetta White, Douglas R Savage, Paul Case, Douglas Blackstock, A William BMC Cancer Research Article BACKGROUND: 5-fluorouracil remains the standard therapy for patients with advanced/metastatic colorectal cancer. Pre-clinical studies have demonstrated the biological modulation of 5-fluorouracil by methotrexate and leucovorin. This phase II study was initiated to determine the activity and toxicity of sequential methotrexate – leucovorin and 5-fluorouracil chemotherapy in patients with advanced colorectal cancer. METHODS: Ninety-seven patients with metastatic colorectal cancer were enrolled onto the study. Methotrexate – 30 mg/m(2) was administered every 6 hours for 6 doses followed by a 2 hour infusion of LV – 500 mg/m(2). Midway through the leucovorin infusion, patients received 5-fluorouracil – 600 mg/m(2). This constituted a cycle of therapy and was repeated every 2 weeks until progression. RESULTS: The median age was 64 yrs (34–84) and the Eastern Cooperative Group Oncology performance score was 0 in 37%, 1 in 55% and 2 in 8% of patients. Partial and complete responses were seen in 31% of patients with a median duration of response of 6.4 months. The overall median survival was 13.0 months. The estimated 1-year survival was 53.7%. Grade III and IV toxic effects were modest and included mucositis, nausea and vomiting. CONCLUSIONS: This phase II study supports previously reported data demonstrating the modest clinical benefit of 5-FU modulation utilizing methotrexate and leucovorin in patients with metastatic colorectal cancer. Ongoing studies evaluating 5-fluorouracil modulation with more novel agents (Irinotecan and/or oxaliplatin) are in progress and may prove encouraging. BioMed Central 2002-05-02 /pmc/articles/PMC113263/ /pubmed/11988109 http://dx.doi.org/10.1186/1471-2407-2-9 Text en Copyright © 2002 Tomlinson et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Tomlinson, Shannon K
Melin, Susan A
Higgs, Vetta
White, Douglas R
Savage, Paul
Case, Douglas
Blackstock, A William
Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title_full Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title_fullStr Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title_full_unstemmed Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title_short Schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase II study
title_sort schedule-selective biochemical modulation of 5-fluorouracil in advanced colorectal cancer – a phase ii study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC113263/
https://www.ncbi.nlm.nih.gov/pubmed/11988109
http://dx.doi.org/10.1186/1471-2407-2-9
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