[1]常娟娟,李太平,康婉英,等.容积旋转调强与调强放疗在宫颈癌放疗中的应用及剂量学、安全性研究[J].陕西医学杂志,2024,(2):194-198.[doi:DOI:10.3969/j.issn.1000-7377.2024.02.010]
 CHANG Juanjuan,LI Taiping,KANG Wanying,et al.Application,dosimetric and safety analysis of volumetric modulated arc therapy and intensity modulated radiation therapy in radiotherapy of cervical cancer[J].,2024,(2):194-198.[doi:DOI:10.3969/j.issn.1000-7377.2024.02.010]
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容积旋转调强与调强放疗在宫颈癌放疗中的应用及剂量学、安全性研究
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《陕西医学杂志》[ISSN:1000-7377/CN:61-1281/TN]

卷:
期数:
2024年2期
页码:
194-198
栏目:
临床研究
出版日期:
2024-02-05

文章信息/Info

Title:
Application,dosimetric and safety analysis of volumetric modulated arc therapy and intensity modulated radiation therapy in radiotherapy of cervical cancer
作者:
常娟娟李太平康婉英张 飞王光明
(阜阳市肿瘤医院放疗科,安徽 阜阳 236000)
Author(s):
CHANG JuanjuanLI TaipingKANG WanyingZHANG FeiWANG Guangming
(Department of Radiotherapy,Fuyang Cancer Hospital,Fuyang 236000,China)
关键词:
宫颈癌 容积旋转调强 调强放疗 剂量 危及器官 安全性
Keywords:
Cervical cancer Volumetric modulated arc therapy Intensity modulated radiation therapy Dose Organs-at-risk Safety
分类号:
R 737.33
DOI:
DOI:10.3969/j.issn.1000-7377.2024.02.010
文献标志码:
A
摘要:
目的:探究容积旋转调强放疗(VMAT)与调强放疗(IMRT)在宫颈癌根治术后放疗中的应用及剂量学、安全性。方法:选取宫颈癌根治后且拟行放疗的患者60例,根据随机数字表法将其分为VMAT组(30例)和IMRT组(30例),分别给予VMAT治疗与IMRT治疗,对比两组机器跳数、治疗计划执行时间、靶区适形度(CI)和均匀性指数(HI)、危及器官的剂量差异及不良反应等。结果:VMAT组在计划控制点多于IMRT组的情况下,其治疗时间仍短于IMRT组。通过Delta验证,VAMT组患者的3%/3 mm和4%/4 mm γ通过率低于IMRT组(均P<0.05)。VAMT组计划的CI记录与IMRT组比较无统计学差异(P>0.05),但与IMRT组相比,VAMT组的HI更接近于1,差异有统计学意义(P<0.05)。VAMT组直肠的V30、V40、V50低于IMRT组,VAMT组对骨盆、膀胱的V20、V30、V40低于IMRT组(均P<0.05); VAMT组和IMRT组发生胃肠道反应患者分别有9例(30.00%)、14例(46.67%); VAMT组和IMRT组发生膀胱反应的患者分别有3例(10.00%)、5例(16.67%),两组胃肠道、膀胱反应发生率比较均无统计学差异(均P>0.05)。两组疗效及随访期内复发或转移情况对比均无统计学差异(均P>0.05)。结论:在宫颈癌根治术后放疗时,VMAT治疗可时间缩短,且治疗效率及剂量学参数优于IMRT,可有效保护骨盆、直肠和膀胱,安全性好。
Abstract:
Objective:To investigate the application,dosimetric and safety differences between volumetric modulated arc therapy(VMAT)and intensity modulated radiation therapy(IMRT)in radiotherapy of cervical cancer after radical operation.Methods:Sixty patients who underwent radical operation for cervical cancer and planned to receive radiotherapy were selected,and randomly divided into the observation group(30 cases)and the control group(30 cases).The control group was treated with IMRT,while the observation group was treated with VMAT.The monitor unit,treatment plan execution time,Conformal Index(CI)and Homogeneity Index(HI)of target volume,organs-at-risk,and adverse reactions were compared between two groups.Results:In the case of planned control points of VMAT more than those of IMRT,the duration of VMAT was still shorter than that of IMRT.Delta validation found that the pass rates of 3%/3 mm and 4%/4 mm γ in VAMT group were lower than those in IMRT group(all P<0.05).The CI records of VAMT regimen were similar to those of IMRT(P>0.05).Compared with IMRT,HI of VAMT was closer to 1(P<0.05).Rectal V30,V40 and V50 in VAMT group were lower than those in IMRT group.V30,V40 and V50 of the pelvis and bladder in VAMT group were significantly lower than those in IMRT group(all P<0.05).There were 9(30.00%)and 14(46.67%)patients with gastrointestinal reactions in VAMT group and IMRT group,respectively.There were 3(10.00%)and 5(16.67%)patients with bladder reactions in VAMT group and IMRT groups,respectively.There were no statistically significant differences in the incidence rates of gastrointestinal reactions and bladder reactions between the groups(all P>0.05).There was no statistically significant difference between the two groups in terms of efficacy and recurrence/metastasis during the follow-up period(all P>0.05).Conclusion:In radiotherapy after radical operation for cervical cancer,the duration of VMAT is relatively short.In addition,the treatment efficiency and dosimetric parameters are better than IMRT.It also can effectively protect the pelvis,rectum and,bladder,with good safety.

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备注/Memo

备注/Memo:
基金项目:安徽省卫生健康委员会科研项目(AHWJ2021a049)
更新日期/Last Update: 2024-02-05