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Simultaneous integrated boost-intensity modulated radiation therapy for inoperable hepatocellular carcinoma
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Simultaneous integrated boost-intensity modulated radiation therapy for inoperable hepatocellular carcinoma
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Simultaneous integrated boost-intensity modulated radiation therapy for inoperable hepatocellular carcinoma
Simultaneous integrated boost-intensity modulated radiation therapy for inoperable hepatocellular carcinoma
Journal Article

Simultaneous integrated boost-intensity modulated radiation therapy for inoperable hepatocellular carcinoma

2014
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Overview
Purpose The aim of this work was to evaluate the clinical efficacy and safety of simultaneous integrated boost-intensity modulated radiation therapy (SIB-IMRT) in patients with inoperable hepatocellular carcinoma (HCC). Methods and materials A total of 53 patients with inoperable HCC underwent SIB-IMRT using two dose-fractionation schemes, depending on the proximity of gastrointestinal structures. The 41 patients in the low dose-fractionation (LD) group, with internal target volume (ITV) < 1 cm from gastrointestinal structures, received total doses of 55 and 44 Gy in 22 fractions to planning target volume 1 (PTV1) and 2 (PTV2), respectively. The 12 patients in the high dose-fractionation (HD) group, with ITV ≥ 1 cm from gastrointestinal structures, received total doses of 66 and 55 Gy in 22 fractions to the PTV1 and PTV2, respectively. Results Overall, treatment was well tolerated, with no grade > 3 toxicity. The LD group had larger sized tumors (median: 6 vs. 3.4 cm) and greater frequencies of vascular invasion (80.6 vs. 16.7 %) than patients in the HD group ( p  < 0.05 each). The median overall survival (OS) was 25.1 mKonzept ist machbar und sicheronths and the actuarial 2-year local progression-free survival (LPFS), relapse-free survival (RFS), and OS rates were 67.3, 14.7, and 54.7 %, respectively. The HD group tended to show better tumor response (100 vs. 62.2 %, p  = 0.039) and 2-year LPFS (85.7 vs. 59 %, p  = 0.119), RFS (38.1 vs. 7.3 %, p  = 0.063), and OS (83.3 vs. 44.3 %, p  = 0.037) rates than the LD group. Multivariate analysis showed that tumor response was significantly associated with OS. Conclusion SIB-IMRT is feasible and safe for patients with inoperable HCC.