Thermal ablation compared to stereotactic body radiation therapy for hepatocellular carcinoma: A multicenter retrospective comparative study
- PMID: 37314737
- PMCID: PMC10270501
- DOI: 10.1097/HC9.0000000000000184
Thermal ablation compared to stereotactic body radiation therapy for hepatocellular carcinoma: A multicenter retrospective comparative study
Abstract
Background aims: Early-stage HCC can be treated with thermal ablation or stereotactic body radiation therapy (SBRT). We retrospectively compared local progression, mortality, and toxicity among patients with HCC treated with ablation or SBRT in a multicenter, US cohort.
Approach results: We included adult patients with treatment-naïve HCC lesions without vascular invasion treated with thermal ablation or SBRT per individual physician or institutional preference from January 2012 to December 2018. Outcomes included local progression after a 3-month landmark period assessed at the lesion level and overall survival at the patient level. Inverse probability of treatment weighting was used to account for imbalances in treatment groups. The Cox proportional hazard modeling was used to compare progression and overall survival, and logistic regression was used for toxicity. There were 642 patients with 786 lesions (median size: 2.1 cm) treated with ablation or SBRT. In adjusted analyses, SBRT was associated with a reduced risk of local progression compared to ablation (aHR 0.30, 95% CI: 0.15-0.60). However, SBRT-treated patients had an increased risk of liver dysfunction at 3 months (absolute difference 5.5%, aOR 2.31, 95% CI: 1.13-4.73) and death (aHR 2.04, 95% CI: 1.44-2.88, p < 0.0001).
Conclusions: In this multicenter study of patients with HCC, SBRT was associated with a lower risk of local progression compared to thermal ablation but higher all-cause mortality. Survival differences may be attributable to residual confounding, patient selection, or downstream treatments. These retrospective real-world data help guide treatment decisions while demonstrating the need for a prospective clinical trial.
Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases.
Conflict of interest statement
Amit G. Singal is a consultant or advisory boards for Genentech, AstraZeneca, Eisai, Bayer, Exelixis, FujiFilm Medical Sciences, Exact Sciences, Glycotest, GRAIL, Freenome, Universal Dx, and TARGET RWE. Andrew M. Moon is a consultant for TARGET RWE. David A. Gerber is a consultant for Medtronic. Dawn Owenreceived research funding (no salary support) from AstraZeneca and Varian. Honorarium from UptoDate. Michael R. Folkert received research funding (no salary support) from Boston Scientific, Inc. Neehar D. Parikh is a consultant or advisory boards for Fujifilm Medical Sciences, AstraZeneca, Eisai, Bayer, Exelixis, Exact Sciences, Freenome, and Gilead. Paul H. Hayashi: Dr. Hayashi is employed by the US Food and Drug Administration (FDA), but the opinions and conclusions in this paper do not reflect any opinions of the FDA. The FDA has not evaluated the opinions or conclusions in this paper. The remaining authors have no conflicts to report.
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Comment in
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Reply : Understanding survival comparisons in non-randomized treatment comparisons for patients with early-stage HCC.Hepatol Commun. 2023 Sep 15;7(10):e0282. doi: 10.1097/HC9.0000000000000282. eCollection 2023 Oct 1. Hepatol Commun. 2023. PMID: 37708458 Free PMC article. No abstract available.
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Understanding survival comparisons in nonrandomized treatment comparisons for patients with early-stage HCC.Hepatol Commun. 2023 Dec 15;8(1):e0281. doi: 10.1097/HC9.0000000000000281. eCollection 2024 Jan 1. Hepatol Commun. 2023. PMID: 38099862 Free PMC article. No abstract available.
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- Heimbach JK, Kulik LM, Finn RS, Sirlin CB, Abecassis MM, Roberts LR, et al. . AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology. 2018;67:358–380. - PubMed
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