Treatment of Recurrent Glioblastoma Multiforme (rGBM) with Antineoplaston AS2-1 in Combination with Targeted Therapy

S. Burzynski, T. Janicki, S. Beenken
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引用次数: 4

Abstract

Treatment of recurrent glioblastoma multiforme (rGBM) poses a difficult challenge. Therefore, the purpose of this report was to evaluate objective response (OR), progression-free survival (PFS), overall survival (OS), and the incidence of adverse events (AEs) in rGBM patients, age 19-70 years, who were treated with antineoplaston AS2-1 (Astugenal) plus targeted therapy. A retrospective analysis was performed. Tumor response was assessed by gadolinium-enhanced magnetic resonance imaging (MRI). Twenty-nine adult rGBM patients were treated between 9/11/2015 and 06/23/2018. Seven had no prior treatment with bevacizumab elsewhere, had radiologic evidence of rGBM, and had MRI assessment of tumor response. The median treatment time was 101 days (range: 55-208 days). OR was seen in six patients (85.7%) with complete disappearance of gadolinium enhancement in four patients (57.1%) and a 50% or greater reduction in gadolinium enhancement in two patients (28.6%). Progressive disease was seen in one patient (14.3%). The median time to first response was 29 days (range: 22-96 days) while the median duration of response was 141 days (range 55-739+ days). Six- and 12-month PFS was 57% and 19%, respectively while 6- and 12-month OS at was 86% and 54%, respectively. Treatment was well-tolerated with no patients experiencing grade 3 or 4 antineoplaston-related toxicity. Regarding response to treatment and toxicity, AS2-1 plus targeted therapy compares favorably with other reported rGBM therapies. Duration of response was shortened by the ill-advised decision of some patients to discontinue treatment after a tumor response was achieved.  
AS2-1联合靶向治疗复发性多型胶质母细胞瘤
复发性多形性胶质母细胞瘤(rGBM)的治疗是一项艰巨的挑战。因此,本报告的目的是评估年龄在19-70岁的rGBM患者的客观反应(OR)、无进展生存期(PFS)、总生存期(OS)和不良事件发生率,这些患者接受抗弓形虫AS2-1(Astugenal)联合靶向治疗。进行了回顾性分析。肿瘤反应通过钆增强磁共振成像(MRI)进行评估。在2015年9月11日至2018年6月23日期间,29名成人rGBM患者接受了治疗。其中7人之前没有在其他地方接受过贝伐单抗治疗,有rGBM的放射学证据,并对肿瘤反应进行了MRI评估。中位治疗时间为101天(范围:55-208天)。6名患者(85.7%)出现OR,4名患者(57.1%)钆增强完全消失,2名患者(28.6%)钆强化减少50%或以上。1名患者(14.3%)出现进展性疾病。首次反应的中位时间为29天(范围:22-96天),而中位反应持续时间为141天(范围55-739天以上)。6个月和12个月的PFS分别为57%和19%,而6个月或12个月OS分别为86%和54%。治疗耐受性良好,没有患者出现3级或4级抗弓形虫相关毒性。关于治疗反应和毒性,AS2-1加靶向治疗与其他报道的rGBM治疗相比是有利的。一些患者在肿瘤反应后做出了不明智的决定,停止治疗,从而缩短了反应的持续时间。
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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