Adaptive brachytherapy treatment planning for cervical cancer using FDG-PET

被引:84
作者
Lin, Lilie L.
Mutic, Sasa
Low, Daniel A.
LaForest, Richard
Vicic, Milos
Zoberi, Imran
Miller, Tom R.
Grigsby, Perry W.
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Radiol Sci, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Div Nucl Sci, Mallinckrodt Inst Radiol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 67卷 / 01期
关键词
PET; treatment planning; cervix; brachytherapy;
D O I
10.1016/j.ijrobp.2006.08.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: A dosimetric study was conducted to compare intracavitary brachytherapy using both a conventional and a custom loading intended to cover a positron emission tomography (PET)-defined tumor volume in patients with cervix cancer. Methods and Materials: Eleven patients who underwent an [F-18]-fluoro-deoxy-D-glucose (FDG)-PET in conjunction with their first, middle, or last brachytherapy treatment were included in this prospective study. A standard plan that delivers 6.5 Gy to point A under ideal conditions was compared with an optimized plan designed to conform the 6.5-Gy isodose surface to the PET defined volume. Results: A total of 31 intracavitary brachytherapy treatments in conjunction with an FDG-PET were performed. The percent coverage of the target isodose surface for the first implant with and without optimization was 73% and 68% (p = 0.21). The percent coverage of the target isodose surface for the mid/final implant was 83% and 70% (p = 0.02), respectively. The dose to point A was higher with the optimized plans for both the first implant (p = 0.02) and the mid/last implants (p = 0.008). The dose to 2 cm(3) and 5 cm(3) of both the bladder and rectum were not significantly different. Conclusions: FDG-PET based treatment planning allowed for improved dose coverage of the tumor without significantly increasing the dose to the bladder and rectum. (c) 2007 Elsevier Inc.
引用
收藏
页码:91 / 96
页数:6
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