4.7 Article

In Vivo Dosimetry Based on SPECT and MR Imaging of 166Ho-Microspheres for Treatment of Liver Malignancies

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 54, Issue 12, Pages 2093-2100

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.113.119768

Keywords

radioembolization; holmium; SPECT; MRI; SIRT

Funding

  1. Dutch Cancer Society (KWF Kankerbestrijding) [UU2009-4346]
  2. Technology Foundation STW [06069, 06448, 11936]
  3. University Medical Center Utrecht

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Ho-166-pdy(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 Ho-166 radioembolization. Methods: Fifteen patients with unresectable, chemorefractory liver metastases of any origin were enrolled in this phase 1 study and were treated with Ho-166 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 R-2* maps (n = 14). Dosimetry was based on SPECT (n = 15) and MR imaging (n = 9) for all volumes of interest, tumor-to-nontumor (TIN) activity concentration ratios were calculated, and correlation and agreement of MR imaging- and SPECT-based measurements were evaluated. Results: The median overall TIN 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 Ho-166-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.

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