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Volume 20, Issue 11, Pages 1460-1463 (November 2009)


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Hepatic Vein Tumor Thrombus as a Risk Factor for Excessive Pulmonary Deposition of Microspheres during TheraSphere Therapy for Unresectable Hepatocellular Carcinoma

Chad J. Fleming, MDa, James C. Andrews, MDaCorresponding Author Informationemail address, Gregory A. Wiseman, MDb, Denise N. Gansen, CNMTb, Lewis R. Roberts, MBChB, PhDc

Received 15 April 2008; received in revised form 13 July 2009; accepted 16 July 2009.

Purpose

To evaluate the impact of identifiable hepatic vein tumor thrombus on the ability to safely deliver TheraSphere (yttrium 90–containing glass microspheres) for the treatment of hepatocellular carcinoma (HCC).

Materials and Methods

A retrospective review was performed of 87 patients (71 men, 16 women; mean age, 64.5 years; age range, 25–83 y) referred for TheraSphere therapy for HCC during a 2-year period between April 2005 and May 2007. Evaluation included contrast-enhanced computed tomography or magnetic resonance imaging, selective mesenteric angiography, and radionuclide perfusion scintigraphy to measure the arteriovenous shunting through the tumor.

Results

Of the 87 patients, 83 underwent angiography and perfusion scintigraphy; 53 were ultimately treated with 65 glass microsphere infusions. Twelve of 83 were identified as having tumor thrombus in a hepatic vein or extending into the inferior vena cava. The mean lung shunt for the patients with hepatic vein tumor thrombus was 30% (range, 11%–60%), compared with 8.2% (range, 3%–23%) for patients without identifiable tumor thrombus. Two of the 12 patients were treated with reduced doses of glass microspheres, and the remaining 10 were offered alternative therapies.

Conclusions

The presence of hepatic vein tumor thrombus is a risk factor for an increased lung shunt that may prohibit delivery of a therapeutic dose of TheraSphere to hepatic tumor.

a Department of Radiology, Division of Vascular and Interventional Radiology, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905

b Division of Nuclear Medicine, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905

c Department of Internal Medicine, Division of Gastroenterology, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905

Corresponding Author InformationAddress correspondence to J.C.A.

 None of the authors have identified a conflict of interest.

PII: S1051-0443(09)00803-3

doi:10.1016/j.jvir.2009.07.033


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