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Clinical Cancer Research Vol. 10, 4077-4082, June 15, 2004
© 2004 American Association for Cancer Research


Clinical Trials

Phase I Study of Rituximab-CHOP Regimen in Combination with Granulocyte Colony-Stimulating Factor in Patients with Follicular Lymphoma

Nozomi Niitsu1, Miyuki Hayama1, Masataka Okamoto2, Mika Khori1, Masaaki Higashihara1, Jun-ichi Tamaru3 and Masami Hirano2

1 Department of Hematology and Internal Medicine IV, Kitasato University School of Medicine, Kanagawa, Japan; 2 Department of Internal Medicine, Fujita Health University School of Medicine, Toyoake, Japan; and 3 Department of Pathology, Saitama Medical Center, Saitama Medical School, Kawagoe, Japan

Purpose: Rituximab is an anti-CD20 monoclonal antibody, and it is used to treat B-cell lymphomas. Antibody-dependent cellular cytotoxicity (ADCC) is considered one of the mechanisms through which rituximab exerts its effects. Granulocyte colony-stimulating factor (G-CSF) enhances the cytotoxicity of neutrophils through ADCC, and it can be speculated that a combination of rituximab and G-CSF may augment the treatment efficacy of rituximab.

Experimental Design: We administered rituximab with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) treatment with G-CSF to 15 patients with follicular lymphoma, and we investigated the safety and efficacy of this regimen. We investigated ADCC activity in neutrophils and the expression of cell surface antigens including Fc{gamma} receptor type I [Fc{gamma}RI (CD64)] on neutrophils to determine the optimal dose of G-CSF.

Results: Adverse reactions occurred in 14 of 15 patients and consisted mainly of grade 3/4 hematological toxicity. The response rate was 100%, with complete remission in 12 patients (80%) and partial remission in 3 patients (20%). At 14 months, the median length of the observation period, 2 of 12 patients had relapsed. G-CSF administration increased both Fc{gamma}RI expression and ADCC activity. There were no significant differences in the levels of Fc{gamma}RI expression or ADCC activity between the 2 µg/kg G-CSF and 5 µg/kg G-CSF groups, indicating that the optimal dose of G-CSF was 2 µg/kg.

Conclusions: We conclude that the combination of rituximab-CHOP and G-CSF is well tolerated. We plan to carry out a randomized trial to compare efficacy between rituximab-CHOP treatment and treatment with a combination of rituximab-CHOP and G-CSF.




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Copyright © 2004 by the American Association for Cancer Research.