Bone marrow sparing in intensity modulated proton therapy for cervical cancer: Efficacy and robustness under range and setup uncertainties

被引:39
作者
Dinges, Eric [1 ]
Felderman, Nicole [1 ]
McGuire, Sarah [1 ,2 ]
Gross, Brandie [1 ]
Bhatia, Sudershan [1 ,2 ]
Mott, Sarah [2 ]
Buatti, John [1 ,2 ]
Wang, Dongxu [1 ,2 ]
机构
[1] Univ Iowa, Dept Radiat Oncol, Iowa City, IA 52242 USA
[2] Univ Iowa Hosp & Clin, Holden Comprehens Canc Ctr, Iowa City, IA 52242 USA
关键词
Bone marrow sparing; Cervical cancer; Proton; Robustness; ACUTE HEMATOLOGIC TOXICITY; RADIATION-THERAPY; CONCURRENT CHEMOTHERAPY; INTER-FRACTION; RADIOTHERAPY; SENSITIVITY; PROSTATE; OPTIMIZATION; PREDICTORS; CISPLATIN;
D O I
10.1016/j.radonc.2015.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: This study evaluates the potential efficacy and robustness of functional bone marrow sparing (BMS) using intensity-modulated proton therapy (IMPT) for cervical cancer, with the goal of reducing hematologic toxicity. Material and methods: IMPT plans with prescription dose of 45 Gy were generated for ten patients who have received BMS intensity-modulated X-ray therapy (IMRT). Functional bone marrow was identified by F-18-flourothymidine positron emission tomography. IMPT plans were designed to minimize the volume of functional bone marrow receiving 5-40 Gy while maintaining similar target coverage and healthy organ sparing as IMRT. IMPT robustness was analyzed with +/- 3% range uncertainty errors and/or +/- 3 mm translational setup errors in all three principal dimensions. Results: In the static scenario, the median dose volume reductions for functional bone marrow by IMPT were: 32% for V-5Gy, 47% for V-10Gy, 54% for V-20Gy, and 57% for V-40Gy, all with p < 0.01 compared to IMRT. With assumed errors, even the worst-case reductions by IMPT were: 23% for V-5Gy, 37% for V-10Gy, 41% for V-20Gy, and 39% for V-40Gy, all with p < 0.01. Conclusions: The potential sparing of functional bone marrow by IMPT for cervical cancer is significant and robust under realistic systematic range uncertainties and clinically relevant setup errors. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:373 / 378
页数:6
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