You have accessJournal of UrologyKidney Cancer: Basic Research I1 Apr 201072 INTRATUMORAL ADMINISTRATION OF HOLMIUM LOADED MICROSPHERES AS A NOVEL MINIMALLY INVASIVE THERAPY FOR KIDNEY CANCER; AN ANIMAL STUDY Judith Jans, Wouter Bult, Stephanie Kroeze, Freek Beekman, Ruud Bosch, and Frank Nijsen Judith JansJudith Jans More articles by this author , Wouter BultWouter Bult More articles by this author , Stephanie KroezeStephanie Kroeze More articles by this author , Freek BeekmanFreek Beekman More articles by this author , Ruud BoschRuud Bosch More articles by this author , and Frank NijsenFrank Nijsen More articles by this author View All Author Informationhttps://doi.org/10.1016/j.juro.2010.02.120AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookTwitterLinked InEmail INTRODUCTION AND OBJECTIVES The widespread use of cross-sectional imaging techniques resulted in a dramatic increase of incidentally detected small kidney tumours. Less invasive treatments need to be developed to eradicate these masses. Besides partial nephrectomy, minimally invasive techniques presently used include cryoablation and radiofrequency ablation. These thermoablative techniques employ either freezing or heat to eradicate tumours. Here, we present a novel local ablation technique using small (12 μm) holmium-166 acetylacetonate microspheres (166HoAcAc MS). 166Ho, in addition to high-energy beta particles, emits gamma rays that allow for nuclear imaging. Moreover, non-radioactive holmium-165 can be visualized by CT and MRI, due to its high electron density and paramagnetism, respectively. These imaging opportunities offer many advantages such as imaging of the distribution of holmium MS post treatment for direct therapy evaluation and follow-up. The objective of this study was to assess the efficacy of 166HoAcAc MS in a mouse kidney cancer model. METHODS HoAcAc MS were prepared as described by Bult et al. (Pharm Res 2009;26) and neutron irradiated to render them radioactive. 10 μl of the 166HoAcAc MS suspension was administered intratumorally in kidney tumour bearing mice. Post administration CT, SPECT and MRI was performed. At several timepoints after administration of MS mice were sacrificed and tissue was analyzed for presence of tumour-kill, proliferation and apoptosis. RESULTS HoAcAc MS were successfully administered to tumour bearing mice. Post administration CT imaging revealed depots of HoAcAc MS in the kidney. The SPECT images showed selective deposition in the kidney and no leakage of MS to the lungs (Fig 1). As expected, tumours in the control group showed a strong growth over time. In contrast, a striking near-complete tumour-control was observed in the 166HoAcAc treated group. No toxicity was observed. Figure 1. Small animal imaging: CT (top), SPECT (middle) and SPECT-CT fusion (bottom). The yellow arrow indicates the depot of MS. CONCLUSIONS We demonstrate the potential of intratumorally administered 166HoAcAc MS as a local treatment of RCC. In addition to a strong cancer control, it provides powerful multimodality imaging opportunities. We anticipate that this is a powerful novel minimally invasive approach to combat small renal masses. Utrecht, Netherlands© 2010 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 183Issue 4SApril 2010Page: e30-e31 Advertisement Copyright & Permissions© 2010 by American Urological Association Education and Research, Inc.MetricsAuthor Information Judith Jans More articles by this author Wouter Bult More articles by this author Stephanie Kroeze More articles by this author Freek Beekman More articles by this author Ruud Bosch More articles by this author Frank Nijsen More articles by this author Expand All Advertisement Advertisement PDF downloadLoading ...
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