| |
|
|
|
|
|
|
|||
|
Blood, 12 February 2009, Vol. 113, No. 7, pp. 1412-1421. Prepublished online as a Blood First Edition Paper on December 12, 2008; DOI 10.1182/blood-2008-08-175653.
CLINICAL TRIALS AND OBSERVATIONS Phase 1/2 study of fractionated 131I-rituximab in low-grade B-cell lymphoma: the effect of prior rituximab dosing and tumor burden on subsequent radioimmunotherapy1 School of Cancer and Imaging Sciences, University of Manchester, Manchester; 2 Department of Clinical Oncology, Poole Hospital National Health Service (NHS) Foundation Trust, Poole; 3 Cancer Sciences Division, School of Medicine, University of Southampton, Southampton General Hospital, Southampton; 4 Institute of Nuclear Medicine, University College London Hospitals NHS Foundation Trust, London; 5 Department of Nuclear Medicine, Royal Marsden NHS Foundation Trust, Sutton; 6 Department of Nuclear Medicine, Southampton University Hospitals NHS Trust, Southampton; and 7 Department of Nuclear Medicine, Christie Hospital NHS Foundation Trust, Manchester, United Kingdom The effect of induction therapy with multiple doses of rituximab on the subsequent efficacy and toxicity of anti-CD20 radioimmunotherapy is unknown. We evaluated a novel protocol using 4 weekly infusions of 375 mg/m2 rituximab followed by 2 fractions of 131I-rituximab, preceded by a 100-mg/m2 predose of rituximab, in relapsed indolent B-cell lymphoma. Induction therapy with rituximab significantly increased the effective half-life of 131I-rituximab (P = .003) and high serum levels of rituximab after induction therapy correlated with increased effective half-life of the radioimmunoconjugate (P = .009). Patients with large tumor burdens experienced significant increases in the effective half-life of 131I-rituximab between delivery of the first and second fractions (P = .007). Induction therapy with multiple doses of rituximab did not appear to compromise the clinical efficacy or increase toxicity of subsequent 131I-rituximab radioimmunotherapy. The overall response rate was 94%, with complete response rate 50%. The median time to progression was 20 months, significantly longer than for the last qualifying chemotherapy (P = .001). Fractionation of 131I-rituximab allowed cumulative whole-body doses of more than 120 cGy, approximately 60% greater than those previously achieved with a single administration of a murine radioimmunconjugate, to be delivered without significant hematologic toxicity.
This article has been cited by other articles:
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Copyright © 2009 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||