Follow-up imaging after cryoablation of clear cell renal cell carcinoma is feasible using single photon emission computed tomography with <sup>111</sup>In-girentuximab.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 31768601.
- Also identified by DOI 10.1007/s00259-019-04613-z and PMC identifier 7299921.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Detection of residual or recurrent vital renal tumor on follow-up (FU) cross-sectional imaging after ablative therapy is challenging. The specific and high expression levels of carbonic anhydrase IX (CAIX) in clear cell renal cell carcinoma (ccRCC) makes it a suitable target for imaging using radiolabeled anti-CAIX antibody girentuximab. The objective of this study was to evaluate the feasibility of targeted FU imaging 1 month after cryoablation of ccRCC using single photon emission computed tomography (SPECT) after <sup>111</sup>In-labeled girentuximab administration. In this prospective study 16 patients underwent <sup>111</sup>In-girentuximab-SPECT before MR-guided renal cryoablation between February 2015 and September 2018. In case of tumor targeting <sup>111</sup>In-girentuximab-SPECT was repeated 1 month following MR-guided cryoablation. Presence of residual or recurrent vital tumor was assessed on contrast-enhanced cross-sectional imaging during further FU. The standard FU imaging protocol consisted of MRI/CT scans at 1, 3, 6, 12, and 18 months and annually thereafter. A total of 10 (63%) patients showed positive tumor targeting on <sup>111</sup>In-girentuximab-SPECT before cryoablation and 9 ( 56%) were eligible to undergo FU SPECT. Of the 9 <sup>111</sup>In-girentuximab-SPECT FU scans, 8 (89%) were considered negative. One (11%) scan showed uptake suggestive for residual vital tumor. Six months after treatment, FU CT showed contrast enhancement suggestive for residual/recurrent disease in the ablated zone at the site of the <sup>111</sup>In-girentuximab uptake after treatment. During a mean FU of 21 months (range 1-33) no other cases with residual/recurrent disease were detected. FU imaging with <sup>111</sup>In-girentuximab-SPECT is feasible after ccRCC cryoablation and may contribute to early detection of residual or recurrent disease.
Medical subject headings
- Carcinoma, Renal Cell
- Cryosurgery
- Kidney Neoplasms