Acute toxicity of mitoxantrone, chlorambucil and prednisolone (MCP) versusMCP plus rituximab in low-grade non-Hodgkin's lymphoma - Interim results of a phase III trial
M. Herold et al., Acute toxicity of mitoxantrone, chlorambucil and prednisolone (MCP) versusMCP plus rituximab in low-grade non-Hodgkin's lymphoma - Interim results of a phase III trial, ONKOLOGIE, 23(2), 2000, pp. 164-166
Background: Phase I and II studies utilizing the chimeric anti-CD 20 antibo
dy rituximab demonstrate good results in relapsed and resistant follicular
and low-grade lymphoma; in combination with cyclophosphamide, doxorubicin,
vincristine, and prednisone (CHOP) chemotherapy excellent remission rates a
nd survival data have been achieved. These data justify to evaluate the eff
icacy and toxicity of a combination of chemotherapy and rituximab in compar
ison to standard chemotherapy alone in a prospective randomized trial. Incl
uded in this study are untreated patients with advanced follicular lymphoma
(FCL grades I and II) and lymphoplasmocytoid lymphoma as well as mantle ce
ll lymphoma stages III and IV. According to the results of phase I and II t
rials we expect a better quality of remissions resulting in an improved fre
edom from treatment failure (FFTF) and survival in the experimental arm of
the study. Material and Methods: In this trial, MCP (mitoxantrone 8 mg/m(2)
, days 1+2, chlorambucil 3x3 mg/m(2), days 1-5, and prednisolone 25 mg/m(2)
, days 1-5, q4 weeksx8) is compared with the combination of rituximab (R) (
375 mg/m(2), day 1) and MCP (days 3-7) q4 weeksx8. In an interim analysis o
f 30 patients, 15 in each treatment group, the acute toxicity of 52 and 50
matched cycles of MCP and MCP+R, respectively, were evaluated. Both patient
groups are comparable. Results: Counting all adverse events (CTC grades 1-
4) there are 36 events in the MCP+R arm and 14 in the MCP arm. If only adve
rse events of CTC grades 3 and 4 are analyzed, however, the differences are
much less pronounced; only 6 patients in each group had leukopenia or thro
mbocylopenia of grade 3 or 4. When comparing treatment cycles, myelotoxicit
y (CTC grades 3 and 4 concerning leukocytes and CTC grades 2-4 for platelet
s) occurred in 17/50 MCP+R cycles but in only 9/52 MCP cycles. Conclusion:
Our preliminary data regarding acute toxicity suggest a tendency to more ad
verse events in the experimental arm (MCP+R) of our study. In the cohort of
patients analyzed we did not observe severe infusion-related events in the
patients who were treated with rituximab.