Phase 1 trial of hypofractionated stereotactic re-irradiation in combination with nivolumab, ipilimumab, and bevacizumab for recurrent high-grade gliomas.

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2025-02-08 eCollection Date: 2025-01-01 DOI:10.1093/noajnl/vdaf033
Solmaz Sahebjam, Raju R Raval, Peter A Forsyth, Heiko Enderling, Nam D Tran, John A Arrington, Robert Macaulay, Haley K Perlow, Joshua D Palmer, Jayeeta Ghose, Prajwal Rajappa, Pierre Giglio, Zihai Li, Arnold B Etame, Sepideh Mokhtari, Ruben J Cruz-Chamorro, Menal Bhandari, Ram Thapa, Timothy J Robinson, Dung-Tsa Chen, Hsiang-Hsuan Michael Yu
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引用次数: 0

Abstract

Background: Our previous clinical investigation suggested that hypofractionated stereotactic re-irradiation (HFSRT) and PD-1 blockade may act synergistically to enhance the immune response against glioma. This subsequent trial investigated the dual blockade of CTLA4 and PD-1 in combination with HFSRT and bevacizumab.

Methods: This phase I study enrolled eligible patients with bevacizumab-naïve recurrent glioblastoma or anaplastic astrocytoma. Participants received nivolumab, ipilimumab, and bevacizumab concurrently with HFSRT (3000 cGy in 5 fractions). Subsequently, nivolumab, ipilimumab, and bevacizumab were administered for a total of 4 cycles followed by nivolumab and bevacizumab until progression. The primary end point of this study was the safety and tolerability of HFSRT in combination with nivolumab, ipilimumab, and bevacizumab in patients with recurrent HGGs. Secondary end points included 6-month survival and 9-month survival.

Results: Twenty-six patients were treated. Treatment-related adverse events (TRAEs) of grade 3 or 4 were observed in 12 (48%) evaluable patients with no unexpected TRAEs. Six months and 9 months survival were 92% (95% CI, 82-100%) and 75% (95% CI, 60-95%), respectively. The median progression-free survival and overall survival were 7.1 months (95% CI, 5.2-12.2) and 15.6 months (95% CI, 11.3-27.0), respectively.

Conclusions: The combination of HFSRT with ipilimumab, nivolumab, and bevacizumab is safe. Our results underscore the potential synergies between stereotactic re-irradiation and checkpoint immunotherapy in patients with recurrent high-grade gliomas.

低分割立体定向再照射联合纳武单抗、伊匹单抗和贝伐单抗治疗复发性高级别胶质瘤的一期试验。
背景:我们之前的临床研究表明,低分割立体定向再照射(HFSRT)和PD-1阻断可能协同作用,增强对胶质瘤的免疫反应。随后的试验研究了HFSRT和贝伐单抗联合对CTLA4和PD-1的双重阻断。方法:这项I期研究纳入了bevacizumab-naïve复发性胶质母细胞瘤或间变性星形细胞瘤的合格患者。参与者同时接受nivolumab, ipilimumab和bevacizumab与HFSRT (3000 cGy分5次)。随后,纳武单抗、伊匹单抗和贝伐单抗共给予4个周期,随后给予纳武单抗和贝伐单抗,直到进展。本研究的主要终点是HFSRT联合纳武单抗、伊匹单抗和贝伐单抗治疗复发性hgg患者的安全性和耐受性。次要终点包括6个月和9个月的生存期。结果:治疗26例。在12例(48%)可评估的患者中观察到3级或4级治疗相关不良事件(TRAEs),没有意外TRAEs。6个月和9个月生存率分别为92% (95% CI, 82-100%)和75% (95% CI, 60-95%)。中位无进展生存期和总生存期分别为7.1个月(95% CI, 5.2-12.2)和15.6个月(95% CI, 11.3-27.0)。结论:HFSRT联合伊匹单抗、纳武单抗和贝伐单抗是安全的。我们的研究结果强调了立体定向再照射和检查点免疫治疗在复发性高级别胶质瘤患者中的潜在协同作用。
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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来源期刊
CiteScore
6.20
自引率
0.00%
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审稿时长
12 weeks
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