Abstract
In a phase I trial 4-demethoxydaunorubicin (4-dm DNR) was administered as oral capsules once a week to 51 adults with advanced mainly gastrointestinal solid tumors. No fatal toxicity was observed at doses up to 25.0 mg/m2. Dose-limiting granulocytopenia and non-hematologic toxicity developed at dosages greater than or equal to 22.5 mg/m2. No response to the therapy was observed. The plasma concentrations of 4-dm DNR were measured in 4 of the patients.
Originalsprog | Engelsk |
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Tidsskrift | Acta oncologica |
Vol/bind | 27 |
Udgave nummer | 5 |
Sider (fra-til) | 521-5 |
Antal sider | 5 |
ISSN | 0284-186X |
Status | Udgivet - 1988 |