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
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.