放射治疗小儿视通路胶质瘤的最新进展

N. Kim, D. Lim
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引用次数: 5

摘要

视神经通路胶质瘤(OPG)是一种位于视神经、视束或视交叉的罕见肿瘤。OPG的治疗选择包括手术、放射治疗(RT)和化疗。尽管放疗在辅助或挽救目的方面可能提供有利的长期结果,但由于放疗可能的晚期效应,化疗优先的方法越来越多地被采用。与传统的x射线治疗相比,质子束放疗可能允许正常组织免于辐射暴露。因此,质子束放射治疗有望减少放射治疗的并发症。本文讨论了OPG肿瘤预后的最新进展,放射治疗后的晚期毒性,并比较了x线治疗和质子束放射治疗的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Updates on Radiation Therapy for Pediatric Optic Pathway Glioma
Optic pathway glioma (OPG) is a rare tumor located in optic nerve, optic tract, or optic chiasm. Treatment options for OPG include surgery, radiation therapy (RT), and chemotherapy. Although RT may provide favorable long-term outcomes in manner of either adjuvant or salvage aim, chemotherapy-first approach is increasingly performed due to possible late effects of RT. Proton beam RT may allow normal tissue sparing of radiation exposure compared to conventional X-ray treatment. Therefore, proton beam RT is expected to reduce complications from RT. This review discusses the recent updates on oncologic outcomes of OPG, late toxicities following RT, and compares the outcomes between X-ray treatment and proton beam RT.
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