Why the study?
Does an intermittent single high-dosage schedule of adriamycin provide efficacy and safety in patients with malignancies?
Population
96 patients with malignancies
Design
Case_series
Authors
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Supports exploration of intermittent high-dose adriamycin; leaves open its role pending controlled trials.
Does an intermittent single high-dosage schedule of adriamycin provide efficacy and safety in patients with malignancies?
An intermittent single high-dosage schedule of adriamycin (60 mg/m2 I.V. every 3 weeks) is efficacious across various malignancies, but requires a 50-75% dose reduction in patients with impaired liver function to avoid severe toxicity.
Benjamin et al. (1974) studied this question.
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