S. Baruchel et al., A PHASE-I STUDY OF ACIVICIN IN REFRACTORY PEDIATRIC SOLID TUMORS - A PEDIATRIC-ONCOLOGY-GROUP STUDY, Investigational new drugs, 13(3), 1995, pp. 211-216
Forty-two patients with progressive solid tumors and brain tumors were
entered in this Phase I study pf the glutamine antagonist acivicin gi
ven intravenously over thirty minutes daily for five days. The major t
oxicities encountered were myelosuppression and central nervous system
toxicity (nightmares and somnolence). The maximum tolerated dosage on
this schedule was 26 mg/M(2) daily for five days. Six patients includ
ing three patients with brain tumor had stable disease.