Yttrium-90 radioembolization for primary and metastatic liver tumors exhibiting arterial-phase hypovascularity
Abstract
To investigate dosimetry-derived tumor-to-perfused normal tissue ratio (T/N) and corresponding clinical outcomes of patients receiving yttrium-90 radioembolization with glass microspheres for tumors identified as hypovascular on arterial-phase cross-sectional imaging. Patients with hypovascular lesions undergoing 90 Y-RE at a single institution were included. Inclusion criteria were hypodense or hypoattenuating tumors relative to normal liver on arterial phase CT or MRI, excluding necrotic tumors. Pre-treatment planning mapping angiography 99mTc-MAA SPECT/CT was used for multi-compartment dosimetry for T/N estimation. The final cohort comprised 27 patients (median age 68, range 52–85 years), including 13 with Child-Pugh A cirrhosis, and ECOG status of 0 ( n = 15), 1 ( n = 11), and 2 ( n = 1). Tumor types were hepatocellular carcinoma ( n = 11), intrahepatic cholangiocarcinoma ( n = 8), and liver metastases ( n = 8). Treatment strategies included lobar (19%), lobar plus segmentectomy (22%), single segmentectomy (33%) and multiple segmentectomies (30%). The mean index tumor size was 5.7 ± 3.2 cm. Mean tumor and perfused normal tissue doses were 480 ± 314 Gy and 270 ± 138 Gy, respectively. Median T/N ratio on planning SPECT/CT was 1.56 (range 0.28–4.79). Response assessments using mRECIST criteria for index lesions were complete response (41%), partial response (33%), stable disease (22%), and progressive disease (4%). Nine patients experienced Grade 1 adverse events (ALP, ALT, or AST serum markers) with no other adverse events. Calculated T/N ratios were greater than 1.00 for most patients with hypovascular tumors, indicating that tumor uptake of 90 Y may be greater than perceived from arterial-phase cross-sectional imaging. Post-treatment follow-up demonstrated favorable outcomes for this patient population.
Fields of Study & Subjects
Hepatocellular Carcinoma Treatment and Prognosis
Radiopharmaceutical Chemistry and Applications
Peptidase Inhibition and Analysis
Publication details
- Journal / source
- Scientific Reports
- Publisher
- Springer Science and Business Media LLC
- Volume
- 16
- Issue
- 1
- Pages
- 4588–4588
- Publication date
- 15 January 2026
- Language
- EN