鼻咽癌放疗后正常脑组织IMRT与VMAT的剂量学比较研究。

Kainan Shao, Shuang Zheng, Yajuan Wang, Xue Bai, Hongying Luo, Fenglei Du
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引用次数: 1

摘要

背景:放疗是鼻咽癌(NPC)的主要治疗方法。然而,它可以通过照射正常脑组织引起隐性rt诱导的损伤。迄今为止,还没有关于辐射在大脑中的确切位置、相应的辐射剂量及其关系的详细报道。方法:我们分析了803例接受放疗的中国鼻咽癌患者,并使用蒙特利尔神经病学研究所(MNI)空间的CT脑模板,比较不同放疗技术(IMRT或VMAT)的放疗剂量分布的组间差异。结果:高剂量(>50 Gy)辐射的脑区主要位于颞叶和边缘叶部分,易发生放射性损伤。接受高剂量IMRT的脑区主要位于鼻咽肿瘤前部附近,而接受高剂量VMAT的脑区主要位于肿瘤后部附近。在T1期患者中,IMRT和VMAT无显著差异。对于T2期患者,差异分布广泛,VMAT在保护正常脑组织方面具有显著的剂量优势。对于T3期患者,VMAT在颞上回和边缘叶表现出优势,而IMRT在小脑后部表现出优势。对于T4期患者,VMAT在保护正常脑组织方面表现出劣势。这些结果表明,IMRT和VMAT在保留不同T期鼻咽癌患者脑内不同危险器官(OARs)方面具有各自的优势。结论:我们的方法在标准MNI空间中分析中国鼻咽癌患者的剂量学特征,为毒性和剂量学分析提供了更大的便利,定位精度更高。使用这种方法,我们发现了与先前报道的有趣差异:VMAT在保护T4期NPC患者的正常脑组织方面表现出劣势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A detailed dosimetric comparative study of IMRT and VMAT in normal brain tissues for nasopharyngeal carcinoma patients treated with radiotherapy.

A detailed dosimetric comparative study of IMRT and VMAT in normal brain tissues for nasopharyngeal carcinoma patients treated with radiotherapy.

A detailed dosimetric comparative study of IMRT and VMAT in normal brain tissues for nasopharyngeal carcinoma patients treated with radiotherapy.

A detailed dosimetric comparative study of IMRT and VMAT in normal brain tissues for nasopharyngeal carcinoma patients treated with radiotherapy.

Background: Radiotherapy (RT) is the primary treatment for nasopharyngeal carcinoma (NPC). However, it can cause implicit RT-induced injury by irradiating normal brain tissue. To date, there have been no detailed reports on the radiated exact location in the brain, the corresponding radiation dose, and their relationship.

Methods: We analyzed 803 Chinese NPC patients treated with RT and used a CT brain template in a Montreal Neurological Institute (MNI) space to compare the group differences in RT dose distribution for different RT technologies (IMRT or VMAT).

Results: Brain regions that received high doses (>50 Gy) of radiation were mainly located in parts of the temporal and limbic lobes, where radioactive damage often occurs. Brain regions that accepted higher doses with IMRT were mainly located near the anterior region of the nasopharyngeal tumor, while brain regions that accepted higher doses with VMAT were mainly located near the posterior region of the tumor. No significant difference was detected between IMRT and VMAT for T1 stage patients. For T2 stage patients, differences were widely distributed, with VMAT showing a significant dose advantage in protecting the normal brain tissue. For T3 stage patients, VMAT showed an advantage in the superior temporal gyrus and limbic lobe, while IMRT showed an advantage in the posterior cerebellum. For T4 stage patients, VMAT showed a disadvantage in protecting the normal brain tissue. These results indicate that IMRT and VMAT have their own advantages in sparing different organs at risk (OARs) in the brain for different T stages of NPC patients treated with RT.

Conclusion: Our approach for analyzing dosimetric characteristics in a standard MNI space for Chinese NPC patients provides greater convenience in toxicity and dosimetry analysis with superior localization accuracy. Using this method, we found interesting differences from previous reports: VMAT showed a disadvantage in protecting the normal brain tissue for T4 stage NPC patients.

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