强度调节质子治疗保留海马的预防性颅脑照射:与光子治疗的计划比较。

IF 3.4 2区 医学 Q2 ONCOLOGY
Xiaoyan Yin, Xiutong Lin, Guifang Zhang, Yong Yin, Tao Sun
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引用次数: 0

摘要

背景:本研究的目的是评估体积调制弧线治疗(VMAT)、螺旋断层治疗(HT)和调强质子治疗(IMPT)的剂量学特征,并比较两种IMPT方案与共面和非共面光束在保留海马的预防性颅脑照射(PCI)治疗小细胞肺癌(SCLC)中的剂量学差异。方法:入选25例诊断为有限期SCLC并接受PCI治疗的患者。设计了四种治疗方案:VMAT、HT和两种共面和非共面光束的IMPT方案(分别称为IMPT-cop和IMPT-noncop)。处方剂量为25 Gy,按2.5 Gy(RBE)分次给药。在VMAT和HT方案中均对PTV进行了优化。在IMPT方案中,采用多场优化和CTV稳健优化,设置不确定度为3 mm,范围不确定度为3.5%。根据RTOG 0933方案,海马的剂量限为100%体积接受剂量(D100)≤9 Gy,最大剂量(Dmax)≤16 Gy。结果:对于靶区,两种IMPT方案均较VMAT和HT方案显著提高了V100、D98、均匀性指数(HI)和梯度指数(GI)。与其他三种方案相比,HT方案的符合性指数(CI)最高。与VMAT和HT方案相比,两种IMPT方案显著降低海马D100、Dmax和Dmean、双侧眼球和腮腺平均剂量、双侧晶状体和晶状体PRV最大剂量。对于海马D100, IMPT-cop和IMPT-noncop方案分别比VMAT和HT方案降低43.23%、42.55%、41.14%和40.43%。对于海马Dmax, IMPT-cop和IMPT-noncop计划分别比VMAT和HT计划降低8.22%、8.29%、7.86%和7.93%。对于海马Dmean, IMPT-cop和IMPT-noncop方案分别比VMAT和HT方案降低23.1%、22.48%、20.55%和19.91%。VMAT方案对双侧眼球的最大剂量值在四种方案中最低。对比两种IMPT方案,IMPT-cop方案显著降低海马平均剂量,双侧眼球Dmean和Dmax以及双侧晶状体和晶状体PRV的Dmax均高于IMPT-noncop方案。结论:与光子计划相比,质子计划在保留海马的PCI中显著减少了对海马、晶状体、眼球和腮腺的剂量。与共面光束的IMPT方案相比,非共面光束的IMPT方案在眼球和晶状体中显示出剂量学优势,而在海马体中没有剂量节约的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intensity-modulated proton therapy for hippocampal-sparing prophylactic cranial irradiation: a planning comparison with photon therapy.

Background: The purpose of the study was to evaluate the dosimetric characteristics of volumetric modulated arc therapy (VMAT), helical tomotherapy (HT), and intensity-modulated proton therapy (IMPT) and to compare the dosimetric differences between the two IMPT plans with coplanar and non-coplanar beams in prophylactic cranial irradiation (PCI) with hippocampal-sparing for small cell lung cancer (SCLC).

Methods: Twenty-five patients diagnosed with limited-stage SCLC and received PCI were enrolled in the study. Four treatment plans were designed: VMAT, HT, and two IMPT plans with coplanar and non-coplanar beams (referred to as IMPT-cop and IMPT-noncop, respectively). The prescription dose was 25 Gy in 2.5 Gy(RBE) fractions. The PTV was optimized in both the VMAT and HT plans. In IMPT plans, multifield optimization and CTV robust optimization with a 3-mm setup uncertainty and 3.5% range uncertainty were used. According to the RTOG 0933 protocol, the dose limits for the hippocampus were the dose received by 100% volume (D100) ≤ 9 Gy and the maximum dose (Dmax) ≤ 16 Gy.

Results: For the target, the two IMPT plans significantly improved the V100, D98, the homogeneity index (HI) and gradient index (GI) compared with VMAT and HT plans. The HT plans showed the highest conformity index (CI) compared to the other three plans. The two IMPT plans significantly reduced the D100, Dmax and Dmean of the hippocampus, the mean dose of bilateral eyeballs and parotids, the maximum dose of bilateral lenses and lenses PRV compared to the VMAT and HT plans. For D100 in hippocampus, the IMPT-cop and IMPT-noncop plans reduced by 43.23%, 42.55%, 41.14%, and 40.43%, respectively, relative to VMAT and HT plans. For Dmax in hippocampus, the IMPT-cop and IMPT-noncop plans decreased by 8.22%, 8.29%, 7.86%, and 7.93%, respectively, relative to VMAT and HT plans. For hippocampal Dmean, IMPT-cop and IMPT-noncop plans decreased by 23.1%, 22.48%, 20.55%, and 19.91% compared with VMAT and HT plans, respectively. VMAT plans showed the lowest values for the maximum dose to the bilateral eyeballs among the four plans. When comparing the two IMPT plans, IMPT-cop plans significantly reduced the mean dose to the hippocampus, and increased the Dmean and Dmax of bilateral eyeballs, and the Dmax of bilateral lenses and lenses PRV compared to IMPT-noncop plans.

Conclusions: Compared with photon plans, proton plans significantly reduce the dose to the hippocampus, lenses, eyeballs and parotids in hippocampal-sparing PCI. Compared to IMPT plans with coplanar beams, IMPT plans with non-coplanar beams have shown dosimetric advantages in eyeballs and lenses, with no benefit for dose sparing in the hippocampus.

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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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