Fusion dual-tracer SPECT-based hepatic dosimetry predicts outcome after radioembolization for a wide range of tumour cell types

Purpose Fusion dual-tracer SPECT imaging enables physiological rather than morphological voxel-based partitioning and dosimetry for 90 Y hepatic radioembolization (RE). We evaluated its prognostic value in a large heterogeneous cohort of patients with extensive hepatic malignancy. Methods A total of...

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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2015-07, Vol.42 (8), p.1192-1201
Hauptverfasser: Lam, Marnix G. E. H., Banerjee, Arjun, Goris, Michael L., Iagaru, Andrei H., Mittra, Erik S., Louie, John D., Sze, Daniel Y.
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Sprache:eng
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Zusammenfassung:Purpose Fusion dual-tracer SPECT imaging enables physiological rather than morphological voxel-based partitioning and dosimetry for 90 Y hepatic radioembolization (RE). We evaluated its prognostic value in a large heterogeneous cohort of patients with extensive hepatic malignancy. Methods A total of 122 patients with primary or secondary liver malignancy (18 different cell types) underwent SPECT imaging after intraarterial injection of 99m Tc macroaggregated albumin (TcMAA) as a simulation of subsequent 90 Y microsphere distribution, followed by administration of an excess of intravenous 99m Tc-labelled sulphur colloid (TcSC) as a biomarker for functional liver, and a second SPECT scan. TcMAA distribution was used to estimate 90 Y radiation absorbed dose in tumour ( D T ) and in functional liver. Laboratory and clinical follow-up were recorded for 12 weeks after RE, and radiographic responses according to (m)RECIST were evaluated at 3 and 6 months. Dose–response relationships were determined for efficacy and toxicity. Results Patients were treated with a median of 1.73 GBq activity of resin microspheres (98 patients) or glass microspheres (24 patients), in a whole-liver approach (97 patients) or a lobar approach (25 patients). The objective response rate was 41 % at 3 months and 48 % at 6 months. Response was correlated with D T ( P  
ISSN:1619-7070
1619-7089
DOI:10.1007/s00259-015-3048-z