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

Savage Paul, White Douglas R, Higgs Vetta and 4 more

BMC Cancer · 2002

doi:10.1186/1471-2407-2-9 (opens in a new tab)

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Abstract

<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods</p> <p>Ninety-seven patients with metastatic colorectal cancer were enrolled onto the study. Methotrexate – 30 mg/m<sup>2</sup> was administered every 6 hours for 6 doses followed by a 2 hour infusion of LV – 500 mg/m<sup>2</sup>. Midway through the leucovorin infusion, patients received 5-fluorouracil – 600 mg/m<sup>2</sup>. This constituted a cycle of therapy and was repeated every 2 weeks until progression.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>

Abstract licence: CC BY-NC-ND

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