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Interventional MRI-guided catheter placement and real time drug delivery to the central nervous system.介入性磁共振成像引导下的导管置入及向中枢神经系统的实时药物递送。
Expert Rev Neurother. 2016 Jun;16(6):635-9. doi: 10.1080/14737175.2016.1175939. Epub 2016 Apr 20.
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Convection-enhanced delivery in glioblastoma: a review of preclinical and clinical studies.脑胶质瘤中的增强型递送:临床前和临床研究综述。
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Local delivery methods of therapeutic agents in the treatment of diffuse intrinsic brainstem gliomas.治疗弥漫性固有脑桥胶质瘤中治疗药物的局部递送方法。
Clin Neurol Neurosurg. 2016 Mar;142:120-127. doi: 10.1016/j.clineuro.2016.01.007. Epub 2016 Jan 11.
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Nanoliposomal irinotecan with fluorouracil and folinic acid in metastatic pancreatic cancer after previous gemcitabine-based therapy (NAPOLI-1): a global, randomised, open-label, phase 3 trial.奈拉滨脂质体、氟尿嘧啶和亚叶酸联合治疗既往基于吉西他滨方案治疗后的转移性胰腺导管腺癌(NAPOLI-1):一项全球性、随机、开放标签、3 期临床试验。
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Pharmacologic inhibition of histone demethylation as a therapy for pediatric brainstem glioma.组蛋白去甲基化的药理学抑制作为小儿脑干胶质瘤的一种治疗方法。
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Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations.弥漫性内生脑桥胶质瘤的基因组分析确定了三个分子亚群和反复出现的激活型 ACVR1 突变。
Nat Genet. 2014 May;46(5):451-6. doi: 10.1038/ng.2936. Epub 2014 Apr 6.
7
Pharmacokinetics, tumor accumulation and antitumor activity of nanoliposomal irinotecan following systemic treatment of intracranial tumors.纳米脂质体伊立替康全身治疗颅内肿瘤后的药代动力学、肿瘤蓄积及抗肿瘤活性
Nanomedicine (Lond). 2014 Jul;9(14):2099-108. doi: 10.2217/nnm.13.201. Epub 2014 Feb 4.
8
Comparing routes of delivery for nanoliposomal irinotecan shows superior anti-tumor activity of local administration in treating intracranial glioblastoma xenografts.比较纳米脂质体伊立替康的给药途径表明,局部给药在治疗颅内神经胶质瘤异种移植瘤方面具有更好的抗肿瘤活性。
Neuro Oncol. 2013 Feb;15(2):189-97. doi: 10.1093/neuonc/nos305. Epub 2012 Dec 21.
9
Characterization of a diffuse intrinsic pontine glioma cell line: implications for future investigations and treatment.弥漫性内生脑桥胶质瘤细胞系的特征:对未来研究和治疗的影响。
J Neurooncol. 2012 Dec;110(3):305-13. doi: 10.1007/s11060-012-0973-6. Epub 2012 Sep 17.
10
An experimental xenograft mouse model of diffuse pontine glioma designed for therapeutic testing.用于治疗测试的弥漫性脑桥胶质瘤实验性异种移植小鼠模型。
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新型脑干肿瘤治疗方法:动物模型中纳米脂质体伊立替康给药途径的比较。

New therapeutic approaches for brainstem tumors: a comparison of delivery routes using nanoliposomal irinotecan in an animal model.

机构信息

Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, 300 East Superior Street, Tarry 2-709, Chicago, IL, 60611, USA.

Brain Tumor Research Center, Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.

出版信息

J Neurooncol. 2018 Feb;136(3):475-484. doi: 10.1007/s11060-017-2681-8. Epub 2017 Nov 23.

DOI:10.1007/s11060-017-2681-8
PMID:29170909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5807192/
Abstract

Despite the advances in imaging, surgery and radiotherapy, the majority of patients with brainstem gliomas die within 2 years after initial diagnosis. Factors that contribute to the dismal prognosis of these patients include the infiltrative nature and anatomic location in an eloquent area of the brain, which prevents total surgical resection and the presence of the blood-brain barrier (BBB), which reduces the distribution of systemically administered agents. The development of new therapeutic approaches which can circumvent the BBB is a potential path to improve outcomes for these children. Convection-enhanced delivery (CED) and intranasal delivery (IND) are strategies that permit direct drug delivery into the central nervous system and are an alternative to intravenous injection (IV). We treated rats bearing human brainstem tumor xenografts with nanoliposomal irinotecan (CPT-11) using CED, IND, and IV. A single treatment of CED irinotecan had a similar effect on overall survival as multiple treatments by IV route. IND CPT-11 showed significantly increased survival of animals with brainstem tumors, and demonstrated the promise of this non-invasive approach of drug delivery bypassing the BBB when combined with nanoliposomal chemotherapy. Our results indicated that using CED and IND of nanoliposomal therapy increase likelihood of practical therapeutic approach for the treatment of brainstem gliomas.

摘要

尽管在影像学、手术和放疗方面取得了进展,但大多数脑干胶质瘤患者在初始诊断后 2 年内死亡。导致这些患者预后不佳的因素包括肿瘤的浸润性和位于大脑功能区的解剖位置,这使得完全手术切除变得不可能,以及血脑屏障(BBB)的存在,这减少了系统给予药物的分布。开发可以绕过 BBB 的新治疗方法是改善这些儿童预后的潜在途径。增强输送(CED)和鼻内输送(IND)是可以将药物直接递送到中枢神经系统的策略,是静脉注射(IV)的替代方法。我们使用 CED、IND 和 IV 为携带人脑干肿瘤异种移植物的大鼠治疗纳米脂质体伊立替康(CPT-11)。CED 伊立替康单次治疗对总生存期的影响与 IV 途径多次治疗相似。IND CPT-11 显示出脑干肿瘤动物的生存率显著提高,并证明了这种非侵入性的绕过 BBB 的药物输送方法与纳米脂质体化疗联合使用时具有很大的潜力。我们的结果表明,使用 CED 和 IND 的纳米脂质体治疗增加了治疗脑干胶质瘤的实际治疗方法的可能性。