In Vivo Dosimetry Based on SPECT and MR Imaging of166Ho-Microspheres for Treatment of Liver Malignancies
作者
Maarten L. J. Smits,Mattijs Elschot,Maurice A. A. J. van den Bosch,Gerrit H. van de Maat,Alfred D. van het Schip,Bernard A. Zonnenberg,Peter R. Seevinck,Helena M. Verkooijen,Chris J.G. Bakker,Hugo W. A. M. de Jong,Marnix G. E. H. Lam,Johannes F.W. Nijsen
出处
期刊:Journal of nuclear medicine [Society of Nuclear Medicine and Molecular Imaging] 日期:2013-10-17卷期号:54 (12): 2093-2100被引量:90
UNLABELLED: (166)Ho-poly(l-lactic acid) microspheres allow for quantitative imaging with MR imaging or SPECT for microsphere biodistribution assessment after radioembolization. The purpose of this study was to evaluate SPECT- and MR imaging-based dosimetry in the first patients treated with (166)Ho radioembolization. METHODS: Fifteen patients with unresectable, chemorefractory liver metastases of any origin were enrolled in this phase 1 study and were treated with (166)Ho radioembolization according to a dose escalation protocol (20-80 Gy). The contours of all liver segments and all discernible tumors were manually delineated on T2-weighted posttreatment MR images and registered to the posttreatment SPECT images (n = 9) or SPECT/CT images (n = 6) and MR imaging-based R2* maps (n = 14). Dosimetry was based on SPECT (n = 15) and MR imaging (n = 9) for all volumes of interest, tumor-to-nontumor (T/N) activity concentration ratios were calculated, and correlation and agreement of MR imaging- and SPECT-based measurements were evaluated. RESULTS: The median overall T/N ratio was 1.4 based on SPECT (range, 0.9-2.8) and 1.4 based on MR imaging (range, 1.1-3.1). In 6 of 15 patients (40%), all tumors had received an activity concentration equal to or higher than the normal liver (T/N ratio ≥ 1). Analysis of SPECT and MR imaging measurements for dose to liver segments yielded a high correlation (R(2) = 0.91) and a moderate agreement (mean bias, 3.7 Gy; 95% limits of agreement, -11.2 to 18.7). CONCLUSION: With the use of (166)Ho-microspheres, in vivo dosimetry is feasible on the basis of both SPECT and MR imaging, which enables personalized treatment by selective targeting of inadequately treated tumors.