PHASE-II STUDY OF ETOPOSIDE, IFOSFAMIDE, AND MITOXANTRONE FOR THE TREATMENT OF RESISTANT ADULT ACUTE LYMPHOBLASTIC-LEUKEMIA

Citation
G. Schiller et al., PHASE-II STUDY OF ETOPOSIDE, IFOSFAMIDE, AND MITOXANTRONE FOR THE TREATMENT OF RESISTANT ADULT ACUTE LYMPHOBLASTIC-LEUKEMIA, American journal of hematology, 43(3), 1993, pp. 195-199
Citations number
30
Categorie Soggetti
Hematology
ISSN journal
03618609
Volume
43
Issue
3
Year of publication
1993
Pages
195 - 199
Database
ISI
SICI code
0361-8609(1993)43:3<195:PSOEIA>2.0.ZU;2-L
Abstract
Although combination chemotherapy induces complete remission in 60-90% of adults with acute lymphoblastic leukemia, only 20-45% of patients remain in continued remission 5 years from diagnosis. For patients wit h a short first remission, multiple relapses, or patients with disease refractory to initial induction chemotherapy, few salvage treatments are successful. To improve the results of salvage therapy we studied t he efficacy and toxicity of a combination of etoposide (100 mg/m2 IV q d x 5), ifosfamide (1.5 g/m2/d x 5), and mitoxantrone (8 mg/m2/d IV x 3) in 11 adult patients with relapsed or refractory ALL. The median fo llow-up of all patients completing therapy is 208 days (30-484+ days). Eight of 11 (73%; 95% confidence interval 45-92%) achieved a complete remission, two patients failed to enter remission, and one patient di ed of multiorgan system failure shortly after receiving therapy. Media n DFS is 96 days and median survival from remission is 234 days. Five patients who achieved CR subsequently relapsed with a median time to r elapse of 80 days (50-151 days). Median time to granulocyte > .5 X 10( 9)/L was 28 days (21-46 days) and the median time to platelet recovery > 20 x 10(9)/L was 24 days (21-39 days). Although gastrointestinal to xicity was common, no patient developed severe cardiac, hepatic, pulmo nary, or neurologic complications. These results demonstrate that the combination of etoposide, ifosfamide, and mitoxantrone can be used as an effective salvage therapy for patients with resistant ALL.