Surgical adjuvant therapy of large-bowel carcinoma: an evaluation of levamisole and the combination of levamisole and fluorouracil. The North Central Cancer Treatment Group and the Mayo Clinic.

John A. Laurie(Grand Forks Air Force Base), C G Moertel(Mayo Clinic in Arizona), Thomas R. Fleming(Mayo Clinic in Arizona), Harry S. Wieand(Mayo Clinic in Arizona), John E. Leigh(Mayo Clinic in Arizona), Joseph Rubin(Mayo Clinic in Arizona), G McCormack(Mayo Clinic in Arizona), James B. Gerstner(Mayo Clinic in Arizona), James E. Krook(Mayo Clinic in Arizona), James A. Malliard(Mayo Clinic in Arizona)
Journal of Clinical Oncology
October 1, 1989
Cited by 699

Abstract

A total of 401 eligible patients with resected stages B and C colorectal carcinoma were randomly assigned to no-further therapy or to adjuvant treatment with either levamisole alone, 150 mg/d for 3 days every 2 weeks for 1 year, or levamisole plus fluorouracil (5-FU), 450 mg/m2/d intravenously (IV) for 5 days and beginning at 28 days, 450 mg/m2 weekly for 1 year. Levamisole plus 5-FU, and to a lesser extent levamisole alone, reduced cancer recurrence in comparison with no adjuvant therapy. These differences, after correction for imbalances in prognostic variables, were only suggestive for levamisole alone (P = .05) but quite significant for levamisole plus 5-FU (P = .003). Whereas both treatment regimens were associated with overall improvements in survival, these improvements reached borderline significance only for stage C patients treated with levamisole plus 5-FU (P = .03). Therapy was clinically tolerable with either regimen and severe toxicity was uncommon. These promising results have led to a large national intergroup confirmatory trial currently in progress.


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