PubMed · 1997 · 26 citations · 0 references
MedicineOncologyPharmacologyChemotherapyClinical PharmacologyPharmacokinetics Of Anticancer AgentsDose Adjustment In OncologyPharmacokinetics Of Anticancer DrugsToxicity ManagementChemotherapy Dose OptimizationComplete Response AssessmentMaximum Tolerated EffectMetastatic Breast Cancer TreatmentOncology Chemotherapy DosingPharmacokinetic Study DesignPharmacokinetics Of Cytotoxic ChemotherapyTreatment Regimen Modification
This was a phase I dose-finding and pharmacokinetic study of vinorelbine (Navelbine) and docetaxel (Taxotere) as first-line chemotherapy for metastatic breast cancer. Vinorelbine dose, 20 or 22.5 mg/m2, on days 1 and 5, was followed on day 1 by docetaxel every 21 days, in doses increasing from 60 to 100 mg/m2. Two maximum tolerated doses were reached, the first at 75 mg/m2 of docetaxel and 22.5 mg/m2 of vinorelbine, and the second at 100 mg/m2 of docetaxel and 20 mg/m2 of vinorelbine. Symptomatic peripheral neuropathy was not observed. The recommended doses for phase II studies are 75 to 85 mg/m2 of docetaxel on day 1 and 20 mg/m2 of vinorelbine on days 1 and 5, every 3 weeks. The treatment regimen, which included 3-day corticosteroid prophylaxis, resulted in only mild fluid retention. Responses were seen at all dose levels, with an 80% overall response rate at the higher recommended dose; the overall response rate for patients at all dose levels was 66%. A high rate of response, including a complete response, was observed in patients with liver metastases.