Litcius/Paper detail

The Prognostic Value of Quantitative Bone SPECT/CT Before <sup>223</sup>Ra Treatment in Metastatic Castration-Resistant Prostate Cancer

Helmut Dittmann, Sabine Kaltenbach, Matthias Weissinger, Francesco Fiz, Peter Martus, Maren Pritzkow, Juergen Kupferschlaeger, Christian la Fougère

2020Journal of Nuclear Medicine24 citationsDOIOpen Access PDF

Abstract

Radiolabeled bisphosphonates such as <sup>99m</sup>Tc-3,3-diphosphono-1,2-propanodicarboxylic acid (<sup>99m</sup>Tc-DPD) typically show intense uptake in skeletal metastases from metastatic castration-resistant prostate cancer (mCRPC). Extensive bone involvement is regarded as a risk factor for mCRPC patients treated with <sup>223</sup>Ra-dichloride (<sup>223</sup>Ra). The aim of this study was to quantify <sup>99m</sup>Tc-DPD uptake by means of SPECT/CT before <sup>223</sup>Ra and compare the results with the feasibility of treatment and overall survival (OS). <b>Methods:</b> Sixty consecutive mCRPC patients were prospectively included in this study. SPECT/CT of the central skeleton covering the skull to the mid-femoral level was performed before the first cycle of <sup>223</sup>Ra. The bone compartment was defined by means of low-dose CT. Emission data were corrected for scatter, attenuation, and decay supplemented by resolution recovery using dedicated software. The Kaplan–Meier estimator, <i>U</i> test, and Cox regression analysis were used for statistics. <b>Results:</b> Total <sup>99m</sup>Tc-DPD uptake of the central skeleton varied between 11% and 56% of injected dose (%ID) or between 1.8 and 10.5 %ID/1,000 mL of bone volume (%ID/L). SUV<sub>mean</sub> ranged from 1.9 to 7.4, whereas the SUV<sub>max</sub> range was 18–248. Patients unable to complete <sup>223</sup>Ra treatment because of progression and/or cytopenia (<i>n</i> = 23) showed significantly higher uptake (31.9 vs. 25.4 %ID and 6.0 vs. 4.7 %ID/L; <i>P</i> &lt; 0.02). OS after <sup>223</sup>Ra (median, 15.2 mo) was reduced to 7.3 mo in cases of skeletal uptake that was 26 %ID or higher, as compared with 30.8 mo if lower than 26 %ID (<i>P</i> = 0.008). Similar results were obtained for %ID/L and SUV<sub>mean</sub>. SUV<sub>max</sub> did not correlate with survival. %ID/L was identified as an independent prognostic factor for OS (hazard ratio, 1.381 per unit), along with number of previous treatment lines. <b>Conclusion:</b> Quantitative SPECT/CT of bone scans performed at baseline is prognostic for survival in mCRPC patients treated with <sup>223</sup>Ra.

Topics & Concepts

Prostate cancerMedicineOncologyOverall survivalCancerInternal medicineNuclear medicineProstate Cancer Treatment and ResearchRadiopharmaceutical Chemistry and ApplicationsBone health and treatments