Suppr超能文献

联合抗血管生成疗法治疗成人脑干胶质瘤:一例报告及文献综述

Treatment of adult brainstem glioma with combined antiangiogenic therapy: a case report and literature review.

作者信息

Yu Dongdong, Han Guang, Liu Huali, Gao Likun, Verma Vivek

机构信息

Department of Radiation Oncology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, P.R. China.

Department of Radiation Oncology, Hubei Cancer Hospital, Wuhan, Hubei Province, P.R. China,

出版信息

Onco Targets Ther. 2019 Feb 18;12:1333-1339. doi: 10.2147/OTT.S195783. eCollection 2019.

Abstract

Adult brainstem gliomas belong to a rare and heterogeneous group of brain tumors. The overall prognosis is poor; therapeutic options are limited, given the resistance to radiotherapy and the unclear role of chemotherapy/antiangiogenic therapy. Apatinib, a tyrosine kinase inhibitor that selectively inhibits the vascular endothelial growth factor receptor and mildly inhibits c-Kit, PDGFR-β, RET, and c-SRC, has been reported to show efficacy among some patients with malignant supratentorial gliomas. However, its effect on brainstem glioma has not been reported so far. Herein, a 66-year-old man with brainstem anaplastic astrocytoma isocitrate dehydrogenase (IDH) wild type was treated initially with combined radiotherapy, temozolomide, and apatinib. The patient achieved a complete response by MRI and continues to have an ongoing progression-free survival of over 8 months. To our knowledge, this is the first case report using apatinib to treat brainstem IDH wild-type anaplastic astrocytoma, displaying an excellent outcome. We also summarize cases of adult brainstem glioma treated with antiangiogenic therapy. Experiences using various regimens may improve understanding of this rare disease, and thus help physicians to seek more effective treatments for these patients.

摘要

成人脑干胶质瘤属于一类罕见且异质性的脑肿瘤。总体预后较差;鉴于对放疗的耐药性以及化疗/抗血管生成治疗的作用不明确,治疗选择有限。阿帕替尼是一种酪氨酸激酶抑制剂,可选择性抑制血管内皮生长因子受体,并轻度抑制c-Kit、血小板衍生生长因子受体-β(PDGFR-β)、转染重排(RET)和原癌基因酪氨酸蛋白激酶(c-SRC),据报道,它在一些幕上恶性胶质瘤患者中显示出疗效。然而,其对脑干胶质瘤的影响迄今尚未见报道。在此,一名66岁的脑干间变性星形细胞瘤异柠檬酸脱氢酶(IDH)野生型男性患者最初接受了放疗、替莫唑胺和阿帕替尼联合治疗。患者通过磁共振成像(MRI)达到完全缓解,并且持续无进展生存期超过8个月。据我们所知,这是首例使用阿帕替尼治疗脑干IDH野生型间变性星形细胞瘤且疗效优异的病例报告。我们还总结了接受抗血管生成治疗的成人脑干胶质瘤病例。使用各种治疗方案的经验可能会增进对这种罕见疾病的了解,从而帮助医生为这些患者寻找更有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c04/6388961/33bf9b083488/ott-12-1333Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验