Between one and three bolus injections of 0.2-0.3 mL of perflutren lipid microsphere (Definity; Lantheus Medical Imaging, N. Billerica, MA) was injected intravenously and a low-mechanical-index (0.10-0.20) technique was used to dynamically
image any nodule of interest to 5 minutes postinjection. Imaging analysis was performed prospectively and in consensus by three fellowship trained hepatobiliary imagers with 7-11 years of experience. For each nodule, hypervascularity in the arterial phase and hypoenhancement in venous and/or delayed phases relative to the liver were determined. Hypoenhancement on the venous/delayed phase meant the lesion appeared lower in signal than adjacent liver irrespective of its appearance in the arterial phase. Malignancy was considered when a nodule demonstrated arterial hypervascularity and hypoenhancement in the venous or delayed phase relative to the liver. The Selleck PF 2341066 lack of definition of a nodule was the result of the absence of the diagnostic profile. Isodensity in each evaluated phase was considered a negative finding. Biopsy was 3-deazaneplanocin A clinical trial performed using US guidance with an 18-gauge needle (Temno Biopsy System; Allegiance
Systems, McGaw Park, IL) as part of routine clinical practice. Between one and three core biopsies were obtained. Univariate logistic regression analysis was used to determine the findings predictive of HCC. Generalized estimating equations were used to adjust for the correlation between multiple nodules within a patient. Odds ratios (ORs) with confidence intervals were calculated for
each variable; significance was defined as P ≤ 0.05. Sensitivity, specificity, and positive and negative predictive values were calculated for each of the variables with significant association with malignant behavior. Ninety-three indeterminate 1-2-cm nodules were found in 80 patients (Fig. 1). These include 10 nodules in 9 patients, which were detected on contrast-enhanced work-up imaging, selleck compound but not seen on the original surveillance US where another nodule had been detected. In 8 patients (with 8 nodules), final diagnosis could not be established: 6 patients underwent radiofrequency ablation without tissue biopsy or recurrence, and 2 died of non-HCC-related liver failure before 18 months of imaging follow-up. The final diagnosis was established in 85 nodules (72 patients). Benignity was determined in 72 of 85 (85%) nodules by long-term stability on follow-up imaging (mean follow-up, 29.9 months; range, 19-44). Malignancy was determined in 13 of 85 (15%) nodules, 9 by biopsy and 4 by growth, on follow-up imaging (at 13, 14, 24, and 25 months after detection). The 4 malignant nodules detected by growth also exhibited typical HCC enhancement characteristics (i.e., arterial hypervascularity and washout) on follow-up imaging.