The current study will investigate whether a similar distribution pattern can also be observed in human subjects and whether this inhomogeneous distribution is concentrated around the tumour sites. Hepatic arterial injection with 99mTc-MAA and subsequent scintigraphic imaging is widely used to predict the biodistribution of 90Y microspheres, prior

to the actual radioembolization procedure. Its accuracy can however be disputed. In our centre, we have observed that patients with a borderline lung shunt fraction of 10% to 19%, as calculated using the 99mTc-MAA images (approximately Tipifarnib in vivo 24% of all patients, all of whom were instilled a by 50% reduced amount of radioactivity), had no signs of lung shunting on post- 90Y-RE Bremsstrahlung images. In these cases, it seems that the 99mTc-MAA-scan had false-positively predicted extrahepatic spread. This may be explained by the fact that 99mTc-MAA differs in many aspects from the microspheres that are used. Shape, size, density, in-vivo half-life, and number of 99mTc-MAA particles do not resemble the microspheres in any way [13, 31]. In addition, free technetium that is released from the MAA particles can disturb the (correct) assessment of extrahepatic spread. We hypothesize that

a small safety dose with low-activity PLX4032 solubility dmso 166Ho-PLLA-MS will be a more accurate predictor of distribution than 99mTc-MAA. The unique characteristics see more of 166Ho-microspheres, in theory, allow a more accurate prediction of

the distribution with the use of scintigraphy and MRI. In this study, we chose to perform both an injection with 99mTc-MAA and administration of a safety dose of 166Ho-PLLA-MS. The respective distributions of the 99mTc-MAA and the 166Ho-PLLA-MS safety dose will be compared with the distribution of the treatment dose of 166Ho-PLLA-MS by quantitative analysis of the scintigraphic images. Both commercially available 4-Aminobutyrate aminotransferase 90Y-MS products are approved by the Food and Drug Administration (FDA) and European Medicines Agency as a medical device and not as a drug. Radioactive microspheres are a medical device since these implants do not achieve any of their primary intended purposes through chemical action within or on the body and are not dependent upon being metabolized for the achievement of their primary intended purpose. In accordance with the definition of a medical device by the FDA and in analogy with the 90Y-MS, we consider the 166Ho-PLLA-MS to be a medical device [32]. The Dutch medicine evaluation board has discussed this issue (13 July 2007) and has concluded that the microspheres are indeed to be considered as a medical device. One important issue concerning the resin-based SIR-Spheres ® is the relatively high number of particles instilled (>1,000 mg), since this may sometimes be associated with macroscopic embolization as observed during the fluoroscopic guidance [28, 33].