立体定向碘-125近距离治疗低级别胶质瘤的蒙特卡罗研究

Shahrzad Valizadeh, E. Saeedzadeh, A. Zali, H. Nedaei, Saeed Zare Ganjaroodi
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引用次数: 1

摘要

背景:立体定向近距离放射治疗是一种合适的方法,40多年来一直被世界上许多患者用于脑肿瘤和转移治疗。此外,自1979年以来,碘-125近距离放射疗法已被用于脑肿瘤的间质近距离放射治疗。尽管这些植入物的物理和生物学特征使其对微创治疗特别有吸引力,但本文的主要目标是使用蒙特卡罗模型评估不同大小脑胶质瘤肿瘤的I-125种子时间和剂量。方法:在本文中,通过具有20(MBq)活性的Gate代码将蒙特卡罗模拟应用于低级别神经胶质瘤肿瘤治疗的碘种子设计。该来源的剂量测定特征由更新的TG-43U1建议定义。使用Gate代码在液态水中计算种子周围的吸收剂量分布。结果:理想的近距离治疗条件是小于4cm的肿瘤。随着肿瘤尺寸的增大,肿瘤与健康组织交界处的吸收剂量将降低,种子植入时间将增加。结论:在肿瘤内放置碘-125源是不够的,因为肿瘤内的剂量分布不均匀,治疗时间长。使用四个碘-125源可以消除肿瘤,而且在肿瘤中产生均匀的剂量分布,植入时间将分别缩短。
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Stereotactic Iodine-125 Brachytherapy for Low-Grade Glioma Treatment: A Monte Carlo study
Background: Stereotactic brachytherapy is an appropriate method that has been used for brain tumors and metastases treatment for more than 40 years for many patients in the world. Also, iodine-125 brachytherapy has been utilized in brain tumors for interstitial brachytherapy treatment since 1979. Even though the physical and biological features make these implants particularly attractive for minimal invasive treatment, the main goal of this paper is to evaluate the I-125 seed time and dose reached to brain glioma tumors of different sizes for treatment using Monte Carlo modeling. Methods: In this paper, Monte Carlo simulation has been applied by the Gate code with 20 (MBq) activity for an iodine seed design for low-grade glioma tumors treatment. Dosimetry features of this source were defined by the updated TG-43U1 recommendations. The absorbed dose distribution around the seed was calculated using the Gate code in liquid water. Result: The ideal condition for brachytherapy is for tumors smaller than 4 cm. With a larger tumor size, the absorption dose at the border of tumor and healthy tissue will be decreased and the implantation time for seeds will increase. Conclusion: Placing an iodine-125 source inside the tumor is not sufficient because of the non-uniform dose distribution in the tumor and the length of treatment time. Using four iodine-125 sources eliminates the tumor, and also, a uniform dose distribution is created in the tumor and the implantation time will be reduced, respectively.
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