1. A phase II protection study of BB-10010 in patients with high grade non-Hodgkin's lymphoma undergoing intensive chemotherapy.
- Author
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Hough RE, Lorigan PC, Poynton C, Newland A, Gupta RK, Foran J, and Hancock BW
- Subjects
- Adult, Aged, Antineoplastic Combined Chemotherapy Protocols adverse effects, Cell Division drug effects, Chemokine CCL3, Chemokine CCL4, Female, Growth Inhibitors adverse effects, Hematopoietic Stem Cells drug effects, Humans, Lymphoma, T-Cell drug therapy, Male, Middle Aged, Neutropenia chemically induced, Neutropenia prevention & control, Safety, Thrombocytopenia chemically induced, Thrombocytopenia prevention & control, Treatment Failure, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Growth Inhibitors therapeutic use, Lymphoma, Large B-Cell, Diffuse drug therapy, Lymphoma, Non-Hodgkin drug therapy, Macrophage Inflammatory Proteins therapeutic use
- Abstract
The aim of this study was to determine whether administration of BB-10010, a synthetic stem cell inhibitor, would allow more intensive chemotherapy to be administered to patients with newly diagnosed high grade NHL. Thirteen patients were randomised to receive BB-10010 concurrently with dose-intensified BEMOP/CA chemotherapy (7 patients) or chemotherapy alone (6 patients). Although the mean neutrophil count of BB-10010 treated patients was higher following cycles 1, 2 and 3 of chemotherapy compared with those receiving chemotherapy alone, there was no difference in the mean number of cycles tolerated, blood component usage and hospital admissions due to infections. No specific toxicity of BB-10010 was identified. Whilst BB-10010 can be administered safely, it does not improve the ability of patients to tolerate intensive chemotherapy for high grade NHL.
- Published
- 2003
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