4.7 Article

Safety and Efficacy of 166Ho Radioembolization in Hepatocellular Carcinoma: The HEPAR Primary Study

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 63, Issue 12, Pages 1891-1898

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.122.263823

Keywords

hepatocellular carcinoma; radioembolization; holmium; oncology; locoregional treatment

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This study aimed to determine the toxicity profile of 166Ho radioembolization in HCC patients who met certain criteria. The results showed low major toxicity and efficacy, supporting further evaluation.
The safety and efficacy of 166Ho radioembolization was first deter-mined in the HEPAR and HEPAR II studies, which, however, excluded patients with hepatocellular carcinoma (HCC). The aim of this prospec-tive clinical early phase II study was to establish the toxicity profile of 166Ho radioembolization in patients with measurable, liver-dominant HCC; Barcelona clinic liver cancer stage B or C; a Child-Pugh score of no more than B7; and an Eastern Cooperative Oncology Group perfor-mance status of 0-1 without curative treatment options. Methods: The primary endpoint was a rate of unacceptable toxicity defined as grade 3 hyperbilirubinemia (Common Terminology Cancer Adverse Events, version 4.03) in combination with a low albumin or ascites level in the absence of disease progression or treatment-related serious adverse events. Secondary endpoints included overall toxicity, response, sur-vival, change in a-fetoprotein, and quality of life. Thirty-one patients with Barcelona clinic liver cancer stage B (71%) or C (29%) HCC were included, mostly multifocal (87%) or bilobar (55%) disease. Results: Common grade 1 or 2 clinical toxicity included fatigue (71%), back pain (55%), ascites (32%), dyspnea (23%), nausea (23%), and abdom-inal pain (23%), with no more than 10% grade 3-5 toxicity. Grade 3 laboratory toxicity (>10%) included an aspartate transaminase and y-glutamyltransferase increase (16%), hyperglycemia (19%), and lym-phopenia (29%). Treatment-related unacceptable toxicity occurred in 3 of 31 patients. At 3 mo, 54% of target lesions showed a complete or partial response according to modified RECIST. Median overall sur-vival was 14.9 mo (95% CI, 10.4-24.9 mo). No significant changes in quality of life or pain were observed. Conclusion: The safety of 166Ho radioembolization was confirmed in HCC, with less than 10% unac-ceptable toxicity. Efficacy data support further evaluation.

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