首页|宫颈癌调强放射治疗三维在体剂量验证分析及最佳γ通过率阈值

宫颈癌调强放射治疗三维在体剂量验证分析及最佳γ通过率阈值

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目的:对宫颈癌调强放射治疗(IMRT)进行基于电子射野影像装置的三维在体剂量验证(EIVD)分析,研究测量剂量与计划剂量间的差异,并通过剂量学敏感性探讨EIVD质控中最佳γ通过率阈值。方法:回顾性分析浙江大学医学院附属妇产科医院行IMRT的45例宫颈癌患者,所有患者在治疗过程中行EIVD验证,获取测量剂量。采用2 mm/2%、2 mm/3%、3 mm/3%的全局γ指标进行通过率分析,采用剂量体积直方图参数评估测量剂量和计划剂量之间的差异。通过皮尔逊(Pearson)相关性分析研究γ通过率与剂量学差异间的相关性,绘制受试者工作特征(ROC)曲线确定最佳γ通过率阈值。结果:3类γ指标2 mm/2%、2 mm/3%、3 mm/3%的平均通过率分别为(83。07±5。25)%、(91。69±3。52)%、(95。02±2。46)%;EIVD测量剂量与计划剂量在计划靶区(PTV)的平均剂量(Dmean)偏差为2。43%(P=0。016),膀胱、直肠、小肠的Dmean偏差分别为0。35%、0。46%、0。30%(P>0。05)。Pearson分析显示3类γ指标与PTV的剂量偏差相关性较强(r>0。7),与危及器官相关性较弱(r<0。7);ROC分析显示2 mm/2%、2 mm/3%、3 mm/3%最佳的γ通过率阈值分别为79。06%、90。04%、94。19%。结论:EIVD能够有效保证宫颈癌IMRT过程中PTV剂量传递的精准性,利用γ通过率阈值能够为下一步宫颈癌自适应IMRT提供一定的临床依据。
In vivo three-dimensional dose validation for intensity-modulated radiotherapy of cervical cancer and the optimal gamma passing rate threshold
Objective To analyze thein vivo three-dimensional dose verification using electronic portal imaging device(EIVD)for intensity-modulated radiotherapy(IMRT)of cervical cancer for investigating the differences between the measured and planned doses,and explore the optimal threshold for gamma passing rate in EIVD quality control based on dosimetric sensitivity.Methods A retrospective analysis was conducted on a cohort of 45 patients with cervical cancer who underwent IMRT at Women's Hospital,School of Medicine,Zhejiang University.During the treatment,all patients underwent EIVD to obtain the measured doses.The passing rate was analyzed using global gamma criteria of 2 mm/2%,2 mm/3%,and 3 mm/3%.Additionally,dose-volume histogram parameters were utilized to evaluate any differences between the measured and planned doses.Pearson correlation analysis was employed to investigate the relationship between the gamma passing rate and dosimetric differences.Furthermore,receiver operating characteristic(ROC)curve was generated to determine the optimal threshold for the gamma passing rate.Results The average gamma passing rates for the criteria of 2 mm/2%,2 mm/3%,and 3 mm/3%were 83.07%±5.25%,91.69%±3.52%,and 95.02%±2.46%,respectively.The Dmean deviation between EIVD measurement and planned dose in the planning target area was 2.43%(P=0.016),while the Dmean deviations in the bladder,rectum,and small intestine were 0.35%,0.46%,and 0.30%,respectively(P>0.05).Pearson analysis revealed a strong correlation between the 3 gamma indexes and dosimetric differences in the PTV(r>0.7),but a weak correlation with organs-at-risk(r<0.7).ROC analysis indicated that the optimal gamma passing rate thresholds for the criteria of 2 mm/2%,2 mm/3%,and 3 mm/3%were 79.06%,90.04%,and 94.19%,respectively.Conclusion The implementation of EIVD can ensure the accuracy of dose delivery within the PTV during IMRT for cervical cancer.Moreover,establishing a gamma passing rate threshold provides a valuable clinical basis for subsequent adaptive IMRT for cervical cancer.

cervical cancerin vivodose validationdosimetrygamma passing rate

王佳浩、谢洪玲、陈玉凯、唐秋

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浙江大学医学院附属妇产科医院放疗科,浙江杭州 310000

宫颈癌 在体剂量验证 剂量学 γ通过率

浙江省基础公益研究计划

ZCLTGY24H1602

2024

中国医学物理学杂志
南方医科大学,中国医学物理学会

中国医学物理学杂志

CSTPCD
影响因子:0.483
ISSN:1005-202X
年,卷(期):2024.41(7)