PLoS ONE · 2015 · 34 citations · 48 references
MedicineOncologyPharmacologyImmunotherapyMedical OncologyRadionuclide TherapyBeta-particle TherapyRadiation TherapyRadiopharmaceutical TherapyTargeted Cancer TherapyTargeted Radionuclide TherapyTargeted TherapyAntibody-based Radionuclide TherapyNon-hodgkin Lymphoma TherapyNon-hodgkin Lymphoma TreatmentRadiation Toxicity MonitoringRituximab-based TherapyTargeted Therapy ToxicityTumor Growth RateTumor Targeting Specificity
177Lu-DOTA-HH1 (177Lu-HH1) is a novel anti-CD37 radioimmunoconjugate developed to treat non-Hodgkin lymphoma. Mice with subcutaneous Ramos xenografts were treated with different activities of 177Lu-HH1, 177Lu-DOTA-rituximab (177Lu-rituximab) and non-specific 177Lu-DOTA-IgG1 (177Lu-IgG1) and therapeutic effect and toxicity of the treatment were monitored. Significant tumor growth delay and increased survival of mice were observed in mice treated with 530 MBq/kg 177Lu-HH1 as compared with mice treated with similar activities of 177Lu-rituximab or non-specific 177Lu-IgG1, 0.9% NaCl or unlabeled HH1. All mice injected with 530 MBq/kg of 177Lu-HH1 tolerated the treatment well. In contrast, 6 out of 10 mice treated with 530 MBq/kg 177Lu-rituximab experienced severe radiation toxicity. The retention of 177Lu-rituximab in organs of the mononuclear phagocyte system was longer than for 177Lu-HH1, which explains the higher toxicity observed in mice treated with 177Lu-rituximab. In vitro internalization studies showed that 177Lu-HH1 internalizes faster and to a higher extent than 177Lu-rituximab which might be the reason for the better therapeutic effect of 177Lu-HH1.
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Mark Kaminski, Melissa Tuck, Judith Estes et al. · New England Journal of Medicine · 2005 · 715 citations · Full text
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