TY - JOUR T1 - Optical Imaging of Renal Cell Carcinoma with Anti–Carbonic Anhydrase IX Monoclonal Antibody Girentuximab JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 1035 LP - 1040 DO - 10.2967/jnumed.114.137356 VL - 55 IS - 6 AU - Constantijn H.J. Muselaers AU - Alexander B. Stillebroer AU - Mark Rijpkema AU - Gerben M. Franssen AU - Egbert Oosterwijk AU - Peter F.A. Mulders AU - Wim J.G. Oyen AU - Otto C. Boerman Y1 - 2014/06/01 UR - http://jnm.snmjournals.org/content/55/6/1035.abstract N2 - Near-infrared dye-tagged antibodies can be used for the sensitive detection of tumor tissue in vivo. Surgery for clear-cell renal cell carcinoma (ccRCC) might benefit from the use of optical imaging to facilitate the intraoperative detection of carbonic anhydrase IX (CAIX)–expressing tumor lesions with chimeric monoclonal antibody (mAb) girentuximab, which has been shown to have excellent imaging capabilities for ccRCC. Here we studied the potential of fluorescence imaging to detect ccRCC tumors in nude mice with RCC xenografts by using mAb girentuximab conjugated with IRDye800CW; SPECT imaging was used as a reference. Methods: Groups of athymic BALB/c mice with subcutaneous CAIX-positive SK-RC-52 ccRCC tumors were injected intravenously with 125I-labeled girentuximab-IRDye800CW or 125I-labeled girentuximab. For determination of the specificity of the accumulation of the anti-CAIX antibody conjugate in ccRCC, separate groups of mice bearing a CAIX-positive tumor (SK-RC-52) and a CAIX-negative tumor (SK-RC-59) received 125I-girentuximab-IRDye800CW or 125I-labeled MOPC21-IRDye800CW (control mAb). Optical images and micro-SPECT images were acquired until 3 d after injection. Mice were euthanized after the last imaging session, and the biodistribution of the radiolabeled antibody preparations was determined. Results: Optical imaging and micro-SPECT imaging at 1 d after the injection of 125I-girentuximab-IRDye800CW showed clear delineation of the CAIX-expressing ccRCC xenografts, and image contrast improved with time. Fluorescence imaging and biodistribution studies showed high and specific uptake of 125I-girentuximab-IRDye800CW in CAIX-positive ccRCC xenografts (SK-RC-52, 31.5 ± 9.6 percentage injected dose per gram [%ID/g] at 72 h after injection). Tumor uptake was specific, as very low uptake of 125I-girentuximab-IRDye800CW was noted in the CAIX-negative SK-RC-59 tumor (4.1 ± 1.5 %ID/g), and no uptake of 125I-MOPC21-IRDye800CW (control mAb) was noted in the CAIX-positive SK-RC-52 tumor (1.2 ± 0.1 %ID/g). Conclusion: Subcutaneous CAIX-expressing ccRCC xenografts were visualized by optical imaging with 125I-girentuximab-IRDye800CW. Optical images showed good concordance with micro-SPECT images. The accumulation of 125I-girentuximab-IRDye800CW in ccRCC tumors was high and specific. Girentuximab-IRDye800CW potentially could be used for the intraoperative detection of CAIX-expressing tumors and the assessment of residual tumor in resection margins or metastatic lesions in patients with ccRCC. ER -