CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Immunosuppressive therapy using antithymocyte globulin, cyclosporine, and danazol with or without human granulocyte colony-stimulating factor in children with acquired aplastic anemia

A prospective multicenter trial of 119 children 1 to 18 years of age with newly diagnosed aplastic anemia (AA) was conducted, comparing treatment using antithymocyte globulin (ATG), cyclosporine (CyA), and danazol (DAN) with or without rhG-CSF (400 mg/m2, day on days 1-90). All children with very severe AA received rhG-CSF (VSAA group, n 5 50). The other children were randomized to receive ATG, CyA, DAN, and rhG-CSF (G-CSF1 group, n 5 35) or ATG, CyA, and DAN without rhG-CSF (G-CSF2 group, n 5 34). After 6 months, the hematologic response rate was 71%, 55%, and 77% in the VSAA group, G-CSF1 group, and G-CSF2 group, respectively. There was no difference in the incidence of febrile episodes and documented infections between the G-CSF1 and G-CSF2 groups. Bone marrow transplantation (BMT) was attempted in 22 patients in whom initial immunosuppressive therapy (IST; n 5 18) failed or in whom a relapse occurred after an initial response (n 5 4). Nineteen of the 22 patients are alive and well after a median follow-up of 18 months (range, 3 to 66 months) since BMT. The probability of survival at 4 years was 83% 6 7% in the VSAA group, 91% 6 5% in the G-CSF1 group, and 93% 6 6% in the G-CSF2 group. Myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) developed in one patient in each of the three groups; the overall risk for MDS/AML was 3% 6 2% at 4 years. Because the results of IST were encouraging, it is suggested that children with AA receive IST as first-line therapy if there is no human leukocyte antigen-matched sibling donor. (Blood. 2000;96:2049-2054)