Ifosfamide is an alkylating agent with proven efficacy in the treatment of
solid tumours and malignant lymphomas. Because it causes only mild to moder
ate myelosuppression, ifosfamide is often used in combination regimens with
other agents, Ifosfamide has been mainly used in therapy of lymphoma as a
component of salvage regimens, but high-dose ifosfamide is also effective i
n the mobilization of peripheral stem cells for treatment of patients with
relapsed or refractory lymphoma with regimens containing autologous stem ce
ll transplantation. Based on promising data with a new combination regimen
containing idarubicin, etoposide and ifosfamide (IIVP-16) in patients with
poor-risk non-Hodgkin's lymphoma, we have performed a phase II study using
DIZE (dexamethasone 20 mg i.v. days 1-4, idarubicin 8 mg/m(2) i.v. days 1+2
, ifosfamide 1.0 g/m(2) continuous infusion (c.i.) days 1-4, and etoposide
160 mg/m(2) c.i. days 1-4) in patients with relapsed or refractory Hodgkin'
s and non-Hodgkin's lymphoma. In 43 evaluable patients, the response rate w
as 58%, including 11 complete remissions (CR) and 14 partial remissions (PR
). The mean duration of response was 8 months (1-30). Myelosuppression was
generally mild with mean duration of neutropenia < 1000/muL of 2.5 days (ra
nge 0-18) and thrombocytopenia < 25 000/muL of 1.5 days (0-17). Thus, DIZE
is an effective and safe regimen for pretreated patients with aggressive ly
mphoma. These results appear to compare favourably with other salvage regim
ens such as IMVP-16 or DHAP. In conclusion, salvage regimens containing ifo
sfamide can play an important role in patients who are not eligible fur hig
h-dose chemotherapies. Moreover, ifosfamide might also have a role in reduc
ing tumour burden and selecting those patients who qualify for HDCT.