A PHASE-I AND PHASE-II TRIAL OF DOSE-INTENSIFIED CYCLOPHOSPHAMIDE AND GM-CSF IN PEDIATRIC MALIGNANT BRAIN-TUMORS

Purpose: Cyclophosphamide is commonly used in the treatment of children with malignant brain tumors. The purpose of this study was to develop a multicycle, high-dose intensity cyclophosphamide regimen with granulocyte-macrophage colony-stimulating factor (GM-CSF) and to assess its activity against malignant glioma and primitive neuroectodermal tumor (PNET). Methods: Twenty-three patients with brain tumors, including 15 with malignant glioma and six with PNET, were enrolled. Cyclophosphamide (1.8-2.25 g/m(2)/day for 2 days i.v.; total dose 3.6-4.5 g/m(2)) was administered and was followed by recombinant human GM-CSF (5 mu g/kg/day s.c.) on days 3-11 or until the absolute granulocyte count reached 1.5 X 10(9)/L. Results: With a total of 83 cycles administered, the mean dose intensity of cyclophosphamide ranged from 1.5 g/m(2)/week through cycle 2 (22 patients) to 0.8 g/m(2)/week through cycle 8 (two patients). No activity was seen against malignant glioma, and five of six patients with PNET had partial responses. The mean duration of a neutrophil count of <0.5 x 10(9)/L was only 8 days; the platelet recovery was substantially longer. Fever during neutropenia occurred in 54 of 83 cycles. One patient died from transfusion-related graft-versus-host disease.