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- W2010063556 abstract "Radioimmunotherapy is limited by the absorbed dose to radiosensitive organs. Removal of circulating radiolabeled MAbs after tumor tissue has been optimally targeted and should permit the administration of higher radioactivity to patients, resulting in a higher absorbed tumor dose. A novel extracorporeal affinity adsorption treatment (ECAT) device (MitraDep®) was tested, with which biotinylated and radiolabeled MAbs can be removed from the circulation by passing whole blood over a filter coated with avidin. The antibodies were simultaneously radiolabeled and biotinylated using a trifunctional moiety comprising DOTA and biotin. Eight patients—all but 1 of whom with aggressive or mantle cell B-cell lymphoma— who had failed to respond to standard therapies received infusions of 250 mg/m2 cold rituximab and 150 MBq 111In-rituximab-biotin for immunoscintigraphy. A week later, the patients were treated with another 250 mg/m2 rituximab followed by 111In/-90Y-rituximab-biotin (11 or 15 90Y MBq/kg). ECAT was performed 48 hours later. All 8 patients receiving 111In-rituximab-biotin showed tumor uptake. Seven patients received radioimmunotherapy and subsequent ECAT. The mean depletion of 90Y-rituximab-biotin in whole blood after ECAT was 96%, in the whole body 49%, in the lungs 62%, and in the liver and kidneys 40%. No effects on patients' vital signs and no adverse effects on hematological or coagulation parameters was observed during the ECAT procedure. A dose-escalation study is initiated." @default.
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- W2010063556 date "2005-08-01" @default.
- W2010063556 modified "2023-10-02" @default.
- W2010063556 title "A Novel Platform for Radioimmunotherapy: Extracorporeal Depletion of Biotinylated and <sup>90</sup>Y-Labeled Rituximab in Patients with Refractory B-Cell Lymphoma" @default.
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- W2010063556 doi "https://doi.org/10.1089/cbr.2005.20.457" @default.
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