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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...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2002
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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. |
format | Text |
id | pubmed-113263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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