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Stereotactic body radiotherapy for primary hepatocellular carcinoma
David L. Andolino; Cynthia S. Johnson; Mary Maluccio; Paul Kwo; A. Joseph Tector; Jennifer Zook; Peter A.S. Johnstone; Higinia R. Cardenes (Profiled Authors: Paul Y. Kwo; Higinia R. Cardenes; Peter A.S. Johnstone; Jennifer Zook; Mary A. Maluccio; A. Joseph Tector)
International Journal of Radiation Oncology Biology Physics. 2011;81(4):e447-e453.
AbstractPurpose: To evaluate the safety and efficacy of stereotactic body radiotherapy (SBRT) for the treatment of primary hepatocellular carcinoma (HCC). Methods and Materials: From 2005 to 2009, 60 patients with liver-confined HCC were treated with SBRT at the Indiana University Simon Cancer Center: 36 Child-Turcotte-Pugh (CTP) Class A and 24 CTP Class B. The median number of fractions, dose per fraction, and total dose, was 3, 14 Gy, and 44 Gy, respectively, for those with CTP Class A cirrhosis and 5, 8 Gy, and 40 Gy, respectively, for those with CTP Class B. Treatment was delivered via 6 to 12 beams and in nearly all cases was prescribed to the 80% isodose line. The records of all patients were reviewed, and treatment response was scored according to Response Evaluation Criteria in Solid Tumors v1.1. Toxicity was graded according to the Common Terminology Criteria for Adverse Events v4.0. Local control (LC), time to progression (TTP), progression-free survival (PFS), and overall survival (OS) were calculated according to the method of Kaplan and Meier. Results: The median follow-up time was 27 months, and the median tumor diameter was 3.2 cm. The 2-year LC, PFS, and OS were 90%, 48%, and 67%, respectively, with median TTP of 47.8 months. Subsequently, 23 patients underwent transplant, with a median time to transplant of 7 months. There were no ≥Grade 3 nonhematologic toxicities. Thirteen percent of patients experienced an increase in hematologic/hepatic dysfunction greater than 1 grade, and 20% experienced progression in CTP class within 3 months of treatment. Conclusions: SBRT is a safe, effective, noninvasive option for patients with HCC ≤6 cm. As such, SBRT should be considered when bridging to transplant or as definitive therapy for those ineligible for transplant. © 2011 Elsevier Inc.
PMID: 21645977
Scientific Context
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1.
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2.
1999Naga Chalasani; John C. Horlander Sr.; Areen Said; Helena Hoen; Kenyon K. Kopecky; Stephan M. Stockberger Jr.; Rajesh Manam; Paul Y. Kwo; Lawrence Lumeng
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3.
1999R. Saxena; M.Q. Ye; S. Emre; F. Klion; M.A. Nalesnik; S.N. Thung
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