Multi-isocenter stereotactic radiotherapy: Implications for target dose distributions of systematic and random localization errors

被引:4
作者
Ebert, MA
Zavgorodni, SF
Kendrick, LA
Weston, S
Harper, CS
机构
[1] Sir Charles Gairdner Hosp, Dept Radiat Oncol, Nedlands, WA 6009, Australia
[2] Univ Western Australia, Dept Phys, Crawley, WA, Australia
[3] Royal Adelaide Hosp, Dept Med Phys, Adelaide, SA 5000, Australia
[4] Univ Adelaide, Dept Phys & Math Phys, Adelaide, SA 5001, Australia
[5] Medtron Sofamor Danek, Surg Navigat Technol, Louisville, CO USA
[6] Cookridge Hosp, Inst Med Phys & Engn, Yorkshire Ctr Clin Oncol, Leeds Teaching Hosp Trust, Leeds LS16 6QB, W Yorkshire, England
[7] Perth Radiat Oncol Ctr, Wembley, WA, Australia
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2001年 / 51卷 / 02期
关键词
stereotactic radiotherapy; setup errors; misalignment;
D O I
10.1016/S0360-3016(01)01683-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This investigation examined the effect of alignment and localization errors on dose distributions in stereotactic radiotherapy (SRT) with arced circular fields. In particular, it was desired to determine the effect of systematic and random localization errors on multi-isocenter treatments. Methods and Materials: A research version of the FastPlan system from Surgical Navigation Technologies was used to generate a series of SRT plans of varying complexity. These plans were used to examine the influence of random setup errors by recalculating dose distributions with successive setup errors convolved into the off-axis ratio data tables used in the dose calculation. The influence of systematic errors was investigated by displacing isocenters from their planned positions. Results: For single-isocenter plans, it is found that the influences of setup error are strongly dependent on the size of the target volume, with minimum doses decreasing most significantly with increasing random and systematic alignment error. For multi-isocenter plans, similar variations in target dose are encountered, with this result benefiting from the conventional method of prescribing to a lower isodose value for multi-isocenter treatments relative to single-isocenter treatments. Conclusions: It is recommended that the systematic errors associated with target localization in SRT be tracked via a thorough quality assurance program, and that random setup errors be minimized by use of a sufficiently robust relocation system. These errors should also be accounted for by incorporating corrections into the treatment planning algorithm or, alternatively, by inclusion of sufficient margins in target definition. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:545 / 554
页数:10
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