AMSTERDAMAdding granulocyte colony-stimulating factor
(G-CSF) to rituximab may improve response duration and increase the proportion
of complete responses in patients with relapsed B-cell non-Hodgkin’s lymphoma
(NHL). "Although the overall response rate seems comparable to data
reported for rituximab monotherapy, the complete response rate is higher, and
remission duration in this pilot phase-II study is remarkably long,"
Lizette E. van der Kolk, MD, reported in a poster presentation. Dr. van der
Kolk is a member of the Department of Hematology, Academic Medical Center,
Amsterdam, The Netherlands.
Rituximab is marketed as Rituxan in the United States and
MabThera in Europe.
This study included 20 patients who had relapsed after a
maximum of three prior systemic therapies for B-cell NHL. At entry, three
patients were stage II, two patients were stage III, and 15 were stage IV.
Patients received a total of four weekly intravenous doses of
rituximab (375 mg/m2) in combination with a standard subcutaneous dose of G-CSF
(5 µg/kg/d), administered for 3 days, starting 2 days before each rituximab
Longer Remission Duration
The overall response rate was 42% (8/19; 95% CI, 20%-67%).
Five patients (26%) achieved complete remissions (CR) and three patients (16%)
achieved partial remissions (PR). (See Table 1.) One patient was not evaluable.
The median duration of response had not been determined at a
median follow-up of 23 months, but ranged from 4 to more than 25 months. (See
Table 2.) Only one patient who achieved a CR showed progressive disease (after
18 months). The other 4 patients are still in CR for 13+, 24+, 25+, and 25+
months. "In four fifths of patients who achieved a CR, remission duration
was already considerably longer than achieved on last previous
chemotherapy," Dr. van der Kolk said.
The researchers think that rituximab may act through
complement-dependent and antibody-dependent cellular cytotoxicity (ADCC). G-CSF
enhances the cytotoxicity of neutrophils in ADCC, and the goal of testing this
combination was to increase the clinical efficacy of rituximab by the addition
Adverse events occurred almost exclusively during the first
rituximab infusion and mainly consisted of grade 1-2 fever, chills, and
allergic reactions. Toxicity was comparable to that reported for rituximab