HUDDINGE, SWEDENTwo cycles of rituximab (Rituxan) are
effective and well tolerated in patients with symptomatic previously untreated
or first-relapse low-grade lymphomas, reported Eva Kimby, MD. Speaking on
behalf of the Nordic Lymphoma Group, Dr. Kimby, who is in the Department of
Medicine at Huddinge Hospital, in Huddinge, Sweden, said that early data
suggest that the effect of rituximab might be augmented by interferon-alfa-2a
(IFN). This phase-II study included researchers from Sweden, Norway, Denmark,
This randomized trial of rituximab vs rituximab/IFN was
conducted, Dr. Kimby explained, because rituximab is approved for use in
patients with relapsed and refractory follicular lymphoma and because IFN has
immune modulating effects and single-agent efficacy in follicular lymphoma. The
study enrolled patients with symptomatic previously untreated or first- relapse
(< 6 months of low-dose chlorambucil (Leukeran) and/or local radiotherapy)
CD20+ low-grade lymphomas. "All patients had indications for treatment and
did not have low tumor burdens," Dr. Kimby said.
All patients were treated first with rituximab (375 mg/m2 every
week × 4 by IV infusion). Patients were evaluated at weeks 9 and 14. Those in
complete remission (CR) at week 14 were observed with no further treatment
until symptomatic relapse. Patients with stable disease (SD) or progressive
disease (PD) went off study. Those with partial response (PR) or minor response
(MR) were randomized to receive either a second cycle of rituximab 375 mg/m2
every week × 4 or IFN (Roferon) 3 million IU/day SC (week 1), 4.5 million
IU/day (weeks 2-5) in combination with ri-tuximab 375 mg/m2 every week (weeks
Dr. Kimby reported that the study enrolled 127 patients (71
males, 56 females) with "a rather low median age" of 54.1 years
(range 26-75 years). Seventy-six percent had follicular lymphomas. Three
patients were excluded from treatment, leaving 124 patients. Of these, 65% had
stage IV disease, 24% had stage III, and 11% had stage II. Twenty-three percent
had elevated LDH levels, and 18% had more than one extranodal site of disease.
Ninety patients had no previous treatment, 34 had received previous short-term
chlorambucil, 20 had received previous steroids, and 14 had undergone previous
Response data at week 14 following the first cycles of
rituximab were available for 120 of the 124 treated patients and included CR in
11 patients, PR in 56 patients, and MR in 13 patients. (See Table 1.) The 69
patients with PR or MR were randomized to a second treatment cycle of either
rituximab alone (n = 36) or rituximab/IFN (n = 33).
Complete response occurred in
8/36 rituximab patients vs 16/33 rituximab/IFN patients. (See Table 2.) Partial
responses occurred in 20 rituximab patients vs 15 rituximab/IFN patients.
"Rituximab efficacy might be augmented when combined with
interferon," Dr. Kimby said. She also observed that responses were seen in
patients with low- and high-intensity CD20 expression on tumor cells.
Toxicity was mild and mostly related to the first infusion in
both cycles. In cycle 1, 88% of patients reported side effects. In cycle 2, 33
patients had at least one new side effect. Grade 3 reversible thrombocytopenia
occurred in two patients in the rituximab/IFN group. Grade 4 neutropenia
occurred in two patients in the rituximab/IFN group. Grade 3 decrease in liver
function occurred in one patient in the rituximab/IFN group.