A prolonged methoxymorpholino doxorubicin (PNU-152243 or MMRDX) infusion schedule in patients with solid tumours: A phase 1 and pharmacokinetic study

Abstract

The aim of this phase I study was to assess feasibility, pharmacokinetics and toxicity of methoxymorpholino doxorubicin (MMRDX or PNU-152243) administered as a 3 h intravenous infusion once every 4 weeks. Fourteen patients with intrinsically anthracycline-resistant tumours received 37 cycles of MMRDX. The first cohort of patients was treated with 1 mg m-2 of MMRDX. The next cohorts received 1.25 mg m-2 and 1.5 mg m-2 respectively. Common toxicity criteria (CTC) grade III/IV nausea and vomiting were observed in 1/18 cycles at 1.25 mg m-2 and in 2/11 cycles at 1.5 mg m-2. Transient elevation in transaminases up to CTC grade III was observed in 2/16 cycles at 1.25 mg m-2 and 4/11 cycles at 1.5 mg m-2. No cardiotoxicity was observed. At 1.25 mg m-2 CTC grade IV neutropenia occurred in 1/17 cycles. At 1.5 mg m-2 CTC grade III neutropenia was seen in 2/7 and grade IV in 3/7 evaluable cycles. Thrombocytopenia grade III was observed in 2/9 and grade IV in 1/9 evaluable cycles. One patient treated at 1.5 mg m-2 died with neutropenic fever. Therefore, dose-limiting toxicity was reached and 1.25 mg m-2 was considered the maximum tolerated dose for MMRDX as 3 h infusion. No tumour responses were observed. Pharmacokinetic parameters showed a rapid clearance of MMRDX from the circulation by an extensive tissue distribution. Renal excretion of the drug and its metabolite was negligible. In conclusion, prolongation of MMRDX infusion to 3 h does not improve the toxicity profile as compared with bolus administration. (C) 2000 Cancer Research Campaign.