4.1 Article

I-131-cG250 monoclonal antibody immunoscintigraphy versus [F-18]FDG-PET imaging in patients with metastatic renal cell carcinoma: a comparative study

Journal

NUCLEAR MEDICINE COMMUNICATIONS
Volume 23, Issue 3, Pages 229-236

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00006231-200203000-00005

Keywords

renal cell carcinoma; monoclonal antibody cG250; [F-18] FDG-PET; radioimmunoscintigraphy

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The aims of this study were to establish the percentage of metastatic renal cell carcinoma (RCC) lesions detected by radioimmunoscintigraphy (RIS) with the chimeric monoclonal antibody I-131-cG250 versus positron emission tomography (PET) with F-18-labelled deoxyglucose ([F-18]FDG), and to evaluate the use of these radionuclide imaging modalities compared with routinely used imaging techniques. Twenty patients with metastatic RCC disease were examined with [F-18]FDG-PET and I-131-cG250 RIS within 1 week. Total body gamma camera images were obtained up to 120 h after injection of 232 MBq I-131-cG250. Total body PET scanning was performed 45-60 min after intravenous injection of 370 MBq [F-18]FDG. Nuclear medicine techniques were compared to routine imaging procedures. Routine imaging modalities revealed a total of 79 metastases. [F-18]FDG-PET and I-131-cG250 RIS detected 33 previously unknown metastases, of which 32 were [F-18]FDG positive and seven were I-131-cG250 positive. Of the 112 tumour lesions that were documented, [F-18]FDG-PET detected 69% (77 out of 112), whereas I-131-cG250 RIS detected only 30% (34 out of 112). In conclusion, [F-18]FDG-PET is superior to I-131-cG250 RIS in detecting metastases in patients with metastatic RCC, and therefore seems a promising tool for (re)staging patients with RCC. The usefulness of RIS with a diagnostic dose of I-131-cG250 seems to be restricted to selecting patients for radioimmunotherapy with I-131-cG250. (C) 2002 Lippincott Williams Wilkins).

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