A feasibility study of the Nativis Voyager® device in patients with recurrent glioblastoma in Australia.

Q1 Medicine CNS Oncology Pub Date : 2019-03-01 Epub Date: 2019-02-07 DOI:10.2217/cns-2018-0017
Michael Murphy, Anthony Dowling, Christopher Thien, Emma Priest, Donna Morgan Murray, Santosh Kesari
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引用次数: 5

Abstract

Aim: Evaluation of the Nativis Voyager®, an investigational medical device, as monotherapy for recurrent glioblastoma (rGBM).

Materials & methods: A total of 15 patients with rGBM were treated with one of two Voyager ultra-low radio frequency energy cognates: A1A or A2HU. Safety and clinical utility were assessed every 2-4 months.

Results: Median overall survival was 8.04 months in the A1A arm and 6.89 months in the A2HU arm. No serious adverse events associated with Voyager were reported. No clinically relevant trends were noted in clinical laboratory parameters or physical exams.

Conclusion: The data suggest that the Voyager is safe and feasible for the treatment of rGBM.

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澳大利亚对复发性胶质母细胞瘤患者应用native Voyager®设备的可行性研究
目的:评价一种试验性医疗器械“native Voyager®”作为复发性胶质母细胞瘤(rGBM)的单药治疗。材料与方法:共15例rGBM患者接受两种Voyager超低射频能量同源物:A1A或A2HU中的一种治疗。每2-4个月评估一次安全性和临床效用。结果:A1A组的中位总生存期为8.04个月,A2HU组为6.89个月。未报告与Voyager相关的严重不良事件。在临床实验室参数或体格检查中没有发现临床相关的趋势。结论:Voyager治疗rGBM是安全可行的。
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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
期刊最新文献
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