Dahl Nathan A, Liu Arthur K, Foreman Nicholas K, Widener Melissa, Fenton Laura Z, Macy Margaret E
Center for Cancer and Blood Disorders, Children's Hospital Colorado, B-115, 13123 East 16th Avenue, Aurora, CO, 80045, USA.
Morgan Adams Foundation Pediatric Brain Tumor Research Program, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Childs Nerv Syst. 2019 Nov;35(11):2043-2046. doi: 10.1007/s00381-019-04304-y. Epub 2019 Jul 31.
Radiation-induced injury is a well-described toxicity in children receiving radiation therapy for tumors of the central nervous system. Standard therapy has historically consisted primarily of high-dose corticosteroids, which carry significant side effects. Preclinical models suggest that radiation necrosis may be mediated in part through vascular endothelial growth factor (VEGF) overexpression, providing the rationale for use of VEGF inhibitors in the treatment of CNS radiation necrosis. We present the first prospective experience examining the safety, feasibility, neurologic outcomes, and imaging characteristics of bevacizumab therapy for CNS radiation necrosis in children.
Seven patients between 1 and 25 years of age with neurologic deterioration and MRI findings consistent with radiation injury or necrosis were enrolled on an IRB-approved pilot feasibility study. Patients received bevacizumab at a dose of 10 mg/kg intravenously every 2 weeks for up to 6 total doses.
Five patients (83%) were able to wean off corticosteroid therapy during the study period and 4 patients (57%) demonstrated improvement in serial neurologic exams. All patients demonstrated a decrease in T1-weighted post-gadolinium enhancement on MRI, while 5 (71%) showed a decrease in FLAIR signal. Four patients developed a progressive disease of their underlying tumor during bevacizumab therapy.
Our experience lends support to the safety and feasibility of bevacizumab administration for the treatment of radiation necrosis for appropriately selected patients within the pediatric population.
辐射诱导的损伤是接受中枢神经系统肿瘤放射治疗的儿童中一种广为人知的毒性反应。传统上,标准治疗主要包括大剂量皮质类固醇,但会带来显著的副作用。临床前模型表明,放射性坏死可能部分通过血管内皮生长因子(VEGF)的过度表达介导,这为使用VEGF抑制剂治疗中枢神经系统放射性坏死提供了理论依据。我们首次前瞻性地研究了贝伐单抗治疗儿童中枢神经系统放射性坏死的安全性、可行性、神经学结果和影像学特征。
7例年龄在1至25岁之间、出现神经功能恶化且MRI表现符合辐射损伤或坏死的患者参加了一项经机构审查委员会批准的初步可行性研究。患者接受贝伐单抗治疗,剂量为10mg/kg,每2周静脉注射一次,总共最多6次剂量。
5例患者(83%)在研究期间能够停用皮质类固醇治疗,4例患者(57%)在系列神经学检查中表现出改善。所有患者MRI上钆增强后的T1加权像增强均降低,而5例(71%)在液体衰减反转恢复(FLAIR)信号上降低。4例患者在贝伐单抗治疗期间出现了基础肿瘤的进展性疾病。
我们的经验支持了对于儿科人群中适当选择的患者,使用贝伐单抗治疗放射性坏死的安全性和可行性。