High dose stereotactic body radiotherapy using three fractions for colorectal oligometastases

被引:63
作者
Bae, Sun Hyun [1 ]
Kim, Mi-Sook [1 ]
Cho, Chul Koo [1 ]
Kang, Jin-Kyu [1 ]
Kang, Hye Jin [2 ]
Kim, Young Han [3 ]
Shin, Ui-Sup [4 ]
Moon, Sun Mi [4 ]
Lee, Dong Han [5 ]
机构
[1] Korea Inst Radiol & Med Sci, Dept Radiat Oncol, Seoul 139706, South Korea
[2] Korea Inst Radiol & Med Sci, Dept Hemato Oncol, Seoul 139706, South Korea
[3] Korea Inst Radiol & Med Sci, Dept Radiol, Seoul 139706, South Korea
[4] Korea Inst Radiol & Med Sci, Dept Gen Surg, Seoul 139706, South Korea
[5] Korea Inst Radiol & Med Sci, CyberKnife Ctr, Seoul, South Korea
关键词
colorectal cancer; cyberknife; oligometastases; SBRT; PHASE I/II TRIAL; RADIATION-THERAPY; HEPATIC RESECTION; PULMONARY METASTASES; SURGICAL RESECTION; RECURRENCE; LIVER; LUNG; SURVIVAL; CANCER;
D O I
10.1002/jso.23058
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives This study evaluated the treatment result of high dose stereotactic body radiation therapy (SBRT) for colorectal oligometastases. Methods Between 2003 and 2009, 41 patients with 50 lesions confined to one organ from colorectal cancer (CRC) and treated with high dose SBRT =45?Gy were retrospectively reviewed. Lymph nodes (LNs) (18 patients) were the most frequent sites followed in order by lung (12) and liver (11). SBRT doses ranged from 45 to 60?Gy in three fractions (median 48?Gy). The cumulative gross tumor volume (GTV) ranged from 2 to 123?ml (median 13?ml). Results The median follow-up period from the SBRT date was 28 months (range, 665 months). The 3-year local control and overall survival rates were 64 and 60%, and the respective 5-year rates were 57 and 38%. Cumulative GTV and SBRT dose were statistically significant prognostic factors for local control. The grade 3 or 4 complications occurred in three patients (7%). Conclusions High dose SBRT for colorectal oligometastases was found to produce results comparable with surgical series. To improve local control, dose higher than 48?Gy are recommend when possible, but further study will be required to define the optimal normal tissue constraints and acceptable toxicity. J. Surg. Oncol. 2012; 106:138143. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:138 / 143
页数:6
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