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. 2015 May;56(3):561-7.
doi: 10.1093/jrr/rru130. Epub 2015 Feb 16.

Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma

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Survival outcomes after stereotactic body radiotherapy for 79 Japanese patients with hepatocellular carcinoma

Hideomi Yamashita et al. J Radiat Res. 2015 May.

Abstract

Stereotactic body radiotherapy (SBRT) is a relatively new treatment for liver tumor. Outcomes of SBRT for liver tumors unsuitable for ablation or surgical resection were evaluated. A total of 79 patients treated with SBRT for primary hepatocellular carcinoma (HCC) between 2004 and 2012 in six Japanese institutions were studied retrospectively. Patients treated with SBRT preceded by trans-arterial chemoembolization were eligible. Their median age was 73 years, 76% were males, and their Child-Pugh scores were Grades A (85%) and B (11%) before SBRT. The median biologically effective dose (α/β = 10 Gy) was 96.3 Gy. The median follow-up time was 21.0 months for surviving patients. The 2-year overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival were 53%, 40% and 76%, respectively. Sex and serum PIVKA-II values were significant predictive factors for OS. Hypovascular or hypervascular types of HCC, sex and clinical stage were significant predictive factors for PFS. The 2-year PFS was 66% in Stage I vs 18% in Stages II-III. Multivariate analysis indicated that clinical stage was the only significant predictive factor for PFS. No Grade 3 laboratory toxicities in the acute, sub-acute, and chronic phases were observed. PFS after SBRT for liver tumor was satisfactory, especially for Stage I HCC, even though these patients were unsuitable for resection and ablation. SBRT is safe and might be an alternative to resection and ablation.

Keywords: SBRT; hepatocellular carcinoma; stereotactic body radiotherapy.

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Figures

Fig. 1.
Fig. 1.
Overall survival curves by serum PIVKA-II value (over 35 vs under 35 AU/ml). There was no patient with serum PIVKA-II level of just 35 AU/ml.
Fig. 2.
Fig. 2.
Progression-free survival curves by HCC type (hypovascular vs hypervascular).
Fig. 3.
Fig. 3.
Progression-free survival curves by clinical stage (I vs II–III).

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