Abstract

BackgroundTo investigate the clinical and dose–volumetric parameters that predict the risk of radiation-induced liver disease (RILD) for patients with small, unresectable hepatocellular carcinoma (HCC) treated with stereotactic body radiotherapy (SBRT).MethodsBetween March 2007 and December 2009, 92 patients with HCC treated with SBRT were reviewed for RILD within 3 months of completing treatment. RILD was evaluated according to the Common Terminology Criteria for Adverse Events, version 3.0. A dose of 10–20 Gy (median, 15 Gy) per fraction was given over 3–4 consecutive days for a total dose of 30–60 Gy (median, 45 Gy). The following clinical and dose–volumetric parameters were examined: age, gender, Child-Pugh class, presence of hepatitis B virus, gross tumor volume, normal liver volume, radiation dose, fraction size, mean dose to the normal liver, and normal liver volumes receiving from < 5 Gy to < 60 Gy (in increments of 5 Gy).ResultsSeventeen (18.5%) of the 92 patients developed grade 2 or worse RILD after SBRT (49 patients in grade 1, 11 in grade 2, and 6 in ≥ grade 3). On univariate analysis, Child-Pugh class was identified as a significant clinical parameter, while normal liver volume and normal liver volumes receiving from < 15 Gy to < 60 Gy were the significant dose–volumetric parameters. Upon multivariate analysis, only Child-Pugh class was a significant parameter for predicting grade 2 or worse RILD.ConclusionsThe Child-Pugh B cirrhosis was found to have a significantly greater susceptibility to the development of grade 2 or worse RILD after SBRT in patients with small, unresectable HCC. Additional efforts aimed at testing other models to predict the risk of RILD in a large series of HCC patients treated with SBRT are needed.

Highlights

  • To investigate the clinical and dose–volumetric parameters that predict the risk of radiation-induced liver disease (RILD) for patients with small, unresectable hepatocellular carcinoma (HCC) treated with stereotactic body radiotherapy (SBRT)

  • Gross tumor volume (GTV) was delineated based on the visible gross tumor as seen on the computed tomography (CT) images at end-expiratory phase; extension based on movement within the gating phase (30–70%) from the GTV was set as the internal target volume (ITV)

  • The clinical and dose–volumetric parameters analyzed were age, gender, Child-Pugh class, presence of hepatitis B virus (HBV) infection, Eastern Cooperative Oncology HBs-Ag hepatitis B (Group) performance score (ECOG Eastern cooperative oncology group performance score (PS)), GTV, Planning target volume (PTV), normal liver volume, radiation dose, fraction size, mean dose to the normal liver, dose to 33% of the normal liver (D33%), dose to 50% of the normal liver (D50%), and the normal liver volumes receiving from < 5 Gy to < 60 Gy in increments of 5 Gy (respectively, rV5Gy, rV10Gy, rV15Gy, receiving < 20 Gy (rV20Gy), rV25Gy, rV30Gy, rV35Gy, rV40Gy, rV45Gy, rV50Gy, rV55Gy, and rV60Gy)

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Summary

Introduction

To investigate the clinical and dose–volumetric parameters that predict the risk of radiation-induced liver disease (RILD) for patients with small, unresectable hepatocellular carcinoma (HCC) treated with stereotactic body radiotherapy (SBRT). Surgical resection and liver transplantation are the primary treatment modalities for HCC [2,3,4]. Radiofrequency ablation (RFA) can be used with curative intent for small HCC which is unsuitable for surgery [5,6]. Overall, only 30–40% of patients may derive benefit from the various radical curative treatments due to the numerous clinical conditions [7]. In these clinical settings, alternative local therapeutic modalities are urgently needed

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