Hypofractionated stereotactic body radiation therapy (SBRT) for limited hepatic metastases

被引:185
作者
Katz, Alan W. [1 ]
Carey-Sampson, Madeleine [1 ]
Muhs, Ann G. [1 ]
Milano, Michael T. [1 ]
Schell, Michael C. [1 ]
Okunieff, Paul [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Radiat Oncol, Rochester, NY 14642 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 67卷 / 03期
关键词
liver metastases; oligometastases; tolerance; novalis radiosurgery; stereotactic body radiation therapy;
D O I
10.1016/j.ijrobp.2006.10.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the feasibility and efficacy of hypofractionated stereotactic body radiation therapy (SBRT) for the treatment of liver metastases. Methods and Materials: The records of 69 patients with 174 metastatic liver lesions treated with SBRT between April 2001 and October 2004 were reviewed. The most common primary tumors were colorectal (n = 20), breast (n = 16), pancreas (n = 9), and lung (n = 5). The mean number of lesions treated per patient was 2.5 (range, 1-6). The longest diameter of the lesions ranged in size from 0.6 to 12.2 cm (median, 2.7 cm). Dose per fraction ranged from 2 Gy to 6 Gy, with a median total dose of 48 Gy (range, 30-55 Gy). Dose was prescribed to the 100% isodose line (IDL), with the 80% IDL covering the gross tumor volume with a minimum margin of 7 mm. Results: The median follow up was 14.5 months. Sixty patients were evaluable for response based on an abdominal computed tomography scan obtained at a minimum of 3 months after completion of SBRT. The actuarial overall infield local control rate of the irradiated lesions was 76% and 57% at 10 and 20 months, respectively. The median overall survival time was 14.5 months. The progression-free survival rate was 46% and 24% at 6 and 12 months, respectively. None of the patients developed Grade 3 or higher toxicity. Conclusion: Hypofractionated SBRT provides excellent local control with minimal side effects in selected patients with limited hepatic metastases. (c) 2007 Elsevier Inc.
引用
收藏
页码:793 / 798
页数:6
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