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作 者:张先稳[1] 张西志[1] 花威[1] 汪步海[1] 陈婷婷[1] 李军[1]
机构地区:[1]江苏省苏北人民医院放疗科,江苏扬州225001
出 处:《现代肿瘤医学》2015年第17期2503-2505,共3页Journal of Modern Oncology
摘 要:目的:探讨Rapid Arc在前列腺癌放疗中的适用性。方法:对6例前列腺癌患者设计双弧Rapid Arc计划,处方剂量为7600c Gy。用COMPASS系统验证剂量。利用剂量体积直方图分析临床靶区、危及器官OARs的各评价指标。结果:CTV的HI、CI分别为1.08±0.03、0.87±0.06,有较好的均匀性和适合度。PTV的HI、CI稍差。膀胱和直肠的V40仅为(18.98±4.82)%和(20.50±3.03)%,平均剂量也较低,在3000c Gy左右。股骨头D5%也在4000c Gy以内。COMPASS剂量验证所得CTV和PTV各指标差异在4%以内,危及器官评价指标差异在5%以内。等中心处绝对剂量准确率达(99.08±0.66)%,靶区和各危及器官的γ通过率达96%、98%以上。结论:Rapid Arc能够满足前列腺癌放疗的临床剂量学要求。Objective:To study the application suitability of RapidArc for prostate cancer. Methods:We design two arcs RapidArc plan for 6 patients. Prescription dose was 7600cGy. The COMPASS dose verification system was used to verify these plans. Target and organs at risk( OAR)were evaluated with dose-volume histograms( DVH). Results:CTV had good HI,CI,separately was 1. 08 ± 0. 03,0. 87 ± 0. 06. PTV HI,CI slightly worse. The V40 of blad-der and rectum were(18. 98 ± 4. 82)%,(20. 50 ± 3. 03)%. The Dmean was low,at about 3000cGy. The femoral head D5% within 4000cGy. The COMPASS dose verification of CTV and PTV index difference was less than 4%. In addi-tion,organs at risk evaluation index difference was less than 5%. Center absolute dose accuracy was(99. 08 ± 0. 66)%. The gamma pass rates of target and OARs were more than 96%,98%. Conclusion:RapidArc could satisfy the clinical requirements of dose radiotherapy for prostate cancer.
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