AGuIX 纳米粒子与放疗和替莫唑胺联合治疗新诊断的胶质母细胞瘤的 NANO-GBM 试验:1b 期结果和基于 MRI 的生物分布

IF 2.7 3区 医学 Q3 ONCOLOGY Clinical and Translational Radiation Oncology Pub Date : 2024-07-31 DOI:10.1016/j.ctro.2024.100833
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引用次数: 0

摘要

背景在胶质母细胞瘤(GBM)中,肿瘤进展主要发生在受照射的肿瘤体积内。为了应对这一挑战,NANO-GBM 1b/2R 期试验(NCT04881032)正在探索使用静脉注射钆基治疗纳米粒子(AGuIX)的放射增敏策略。材料与方法符合条件的患者年龄在 18 至 75 岁之间,新诊断并经组织学确诊为 GBM,且未完全切除(活检或部分手术)。1b期采用剂量递增法(时间到事件连续再评估法),有三个剂量水平:50、75和100 mg/kg。患者接受RT(60 Gy)治疗,同时辅助TMZ和4次AGuIX注射(D-3/-7、D1、D8和D15)。剂量限制毒性(DLT)定义为任何3-4级不良事件(CTCAE v5.0),不包括脱发、恶心和快速控制的呕吐。结果2022年3月至2023年3月,8名患者入组:1名患者的剂量为50毫克/千克,1名患者的剂量为75毫克/千克,6名患者的剂量为100毫克/千克。所有患者都接受了四次 AGuIX 注射。只有一名患者出现了 DLT(剂量为 100 毫克/千克):3 级淋巴细胞减少症(与 TMZ 有关)。AGuIX的RP2D被确定为100毫克/千克。AGuIX的平均AUC随剂量增加而增加。GBM中AGuIX浓度为中度(36-123 µM)、高度(123-291 µM)或极高度(291 µM)的区域平均分别占38.7%和26.8%。这支持将 AGuIX 的 RP2D 设为 100 毫克/千克(注射 4 次),进入随机 2 期研究。
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NANO-GBM trial of AGuIX nanoparticles with radiotherapy and temozolomide in the treatment of newly diagnosed Glioblastoma: Phase 1b outcomes and MRI-based biodistribution

Background

In glioblastoma (GBM), tumor progression occurs mainly within the irradiated tumor volume. To address this challenge, a radiosensitization strategy with intravenous gadolinium-based theranostic nanoparticles (AGuIX) is being explored in the NANO-GBM phase1b/2R trial (NCT04881032). Here, we present the results of the phase 1b part, which is the first-in-human use of these nanoparticles with radiotherapy and chemotherapy for the treatment of newly diagnosed GBM.

Material and Methods

Eligible patients were aged 18 to 75 years with newly diagnosed and histologically confirmed GBM, with incomplete resection (biopsy or partial surgery). The phase 1b part was a dose escalation approach (Time-to-event Continuous Reassessment Method) with three dose levels: 50, 75, and 100 mg/kg. Patients were treated with RT (60 Gy), and concomitant and adjuvant TMZ, and 4 injections of AGuIX (D-3/-7, D1, D8, and D15). Dose-limiting-toxicity (DLT) was defined as any grade 3–4 adverse event (CTCAE v5.0), excluding alopecia, nausea, and rapidly controlled vomiting. Pharmacokinetic (PK), and biodistribution based on MRI were evaluated.

Results

Between March 2022 and March 2023, eight patients were enrolled: 1 at 50 mg/kg, 1 at 75 mg/kg, and 6 at 100 mg/kg. All patients received the four AGuIX injections. Only one patient experienced a DLT (at 100 mg/kg): a grade 3 lymphopenia (related to TMZ). The RP2D of AGuIX was determined as 100 mg/kg. AGuIX mean AUC increased with dose. Regions of GBM with moderate (36–123 µM), and high (123–291 µM) or very high (>291 µM) AGuIX concentrations accounted in average for 38.7 and 26.8 %, respectively.

Conclusion

These results confirm the lack of AGuIX-related toxicity and the widespread dispersion of nanoparticles throughout GBM. This supports progression to the randomized phase 2 part, utilizing an RP2D of AGuIX of 100 mg/kg (4 injections).

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来源期刊
Clinical and Translational Radiation Oncology
Clinical and Translational Radiation Oncology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.30
自引率
3.20%
发文量
114
审稿时长
40 days
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