Superselective intraarterial cerebral infusion of cetuximab with blood brain barrier disruption combined with Stupp Protocol for newly diagnosed glioblastoma.

Q3 Pharmacology, Toxicology and Pharmaceutics
Kay O Kulason, Julia R Schneider, Shamik Chakraborty, Christopher G Filippi, Bidyut Pramanik, Tamika Wong, Sherese Fralin, Karissa Tan, Ashley Ray, Rachel A Alter, Rafael Ortiz, Alexis Demopoulos, David J Langer, John A Boockvar
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Abstract

Objective: We describe the first case of a novel treatment for a newly diagnosed glioblastoma (GBM) using superselective intraarterial cerebral infusion (SIACI) of cetuximab after osmotic disruption of the blood-brain barrier (BBB) with mannitol. A 51year-old female underwent craniotomy for removal of a right frontal GBM. Pathology confirmed EGFR amplification, and she underwent three treatments of SIACI of cetuximab to the tumor site. The first treatment was given within a week of starting standard of care chemoradiation (Stupp protocol), which is a combination of radiation treatment (2 Gy per/ day x 30 days, total of 60 Gy) and oral temozolomide (75 mg/m2). The second and third SIACI of cetuximab were administered 3 and 6 months later, while the patient continued on maintenance temozolomide. Post-radiation changes on MRI were stable, and there were no signs of recurrence at 4 and 6 months post-resection. Herein, we detail the technical aspects of this novel treatment paradigm and suggest that SIACI of cetuximab after BBB disruption using mannitol, combined with the standard of care chemoradiation therapy, may be an effective treatment method for newly diagnosed EGFR amplified glioblastoma.

超选择性脑动脉灌注西妥昔单抗合并血脑屏障破坏联合Stupp方案治疗新诊断的胶质母细胞瘤。
目的:我们描述了在甘露醇渗透破坏血脑屏障(BBB)后,使用西妥昔单抗超选择性脑动脉输注(SIACI)治疗新诊断的胶质母细胞瘤(GBM)的第一例新疗法。一名51岁女性接受开颅手术切除右额部GBM。病理证实EGFR扩增,患者接受了三次西妥昔单抗对肿瘤部位的SIACI治疗。第一次治疗在开始标准护理放化疗(Stupp方案)的一周内进行,这是放射治疗(2 Gy /天x 30天,总计60 Gy)和口服替莫唑胺(75 mg/m2)的组合。第二次和第三次西妥昔单抗SIACI分别在3个月和6个月后给予,同时患者继续使用替莫唑胺维持治疗。放疗后MRI变化稳定,术后4、6个月无复发迹象。在此,我们详细介绍了这种新治疗模式的技术方面,并建议在使用甘露醇破坏血脑屏障后西妥昔单抗的SIACI,结合标准护理放化疗,可能是新诊断的EGFR扩增胶质母细胞瘤的有效治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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