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14 - 90Yttrium radioembolization for hepatocellular carcinoma

from Section III - Organ-specific cancers – primary liver cancers

Published online by Cambridge University Press:  05 September 2016

Ryan M. Hickey
Affiliation:
Northwestern University
Riad Salem
Affiliation:
Hadassah Hebrew University Medical Center
Robert J. Lewandowski
Affiliation:
Northwestern University
Jean-Francois H. Geschwind
Affiliation:
Yale University School of Medicine, Connecticut
Michael C. Soulen
Affiliation:
Department of Radiology, University of Pennsylvania Hospital, Philadelphia
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Summary

Radioembolization refers to the intra-arterial, transcatheter administration of micrometer-sized particles loaded with a radioisotope, most commonly yttrium-90 (Y90). Because liver tumors derive the majority of their blood supply from hepatic arteries, as opposed to the predominantly portal venous blood supply of normal liver tissue, hepatic arterial injection of Y90-labeled microspheres results in greater deposition of the spheres in tumor tissue as opposed to normal liver parenchyma. Since Y90 radioembolization provides an internal source of radiation to hepatic tumors, it is considered brachytherapy.

Preferential deposition of radioactive microspheres within tumor tissue provides for relative sparing of the uninvolved liver parenchyma from the radiation effects of Y90, thereby permitting significantly higher radiation doses than can be safely administered using external-beam radiation. The radiosensitive nature of normal liver tissue has traditionally limited the role of external-beam radiation in the treatment of primary and metastatic hepatic malignancies, as the incidence of severe radiation-induced liver disease (RILD) may exceed 50% for external-beam radiation doses greater than 35–40 Gy. However, with radioembolization, radiation doses in excess of 150 Gy can be safely administered.

Y90, a pure beta emitter with a half-life of 64.2 hours and tissue penetration of 2.5–11 mm, is incorporated into glass or resin microspheres ranging in size from 20–30 μm (glass) to 20–60 μm (resin). Glass microspheres (Therasphere, BTG International Canada, Ottawa, ON, Canada) were approved in 1999 by the US Food and Drug Administration (FDA) under a Humanitarian Device Exemption for the treatment of unresectable hepatocellular carcinoma (HCC). Resin microspheres (SIR-Spheres, Sirtex Medical, Lane Cove, Australia) were granted full premarketing approval in 2002 by the US FDA for the treatment of unresectable colorectal metastases in conjunction with intrahepatic floxuridine.

Safe and effective treatment of hepatic tumors with radioembolization requires not only the angiographic and endovascular skills critical for selective embolization procedures, but also a comprehensive understanding of radiation administration and safety, including radiation dosimetry and radiation dose modification based on tumor characteristics and a patient's clinical profile.

Patient selection

The patient selection process for Y90 radioembolization involves an assessment of the patient's burden of disease, hepatic biochemical profile, and performance status. Patients should have no extrahepatic disease and a tumor burden less than 70% of the liver volume.

Type
Chapter
Information
Interventional Oncology
Principles and Practice of Image-Guided Cancer Therapy
, pp. 128 - 133
Publisher: Cambridge University Press
Print publication year: 2016

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References

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