NANO-GBM trial of AGuIX nanoparticles with radiotherapy and temozolomide in the treatment of newly diagnosed Glioblastoma: Phase 1b outcomes and MRI-based biodistribution

被引:2
|
作者
Biau, J. [1 ,2 ,3 ,4 ]
Durando, X. [2 ,3 ,4 ,5 ,6 ]
Boux, F. [3 ]
Molnar, I. [1 ,2 ,4 ]
Moreau, J. [1 ,2 ]
Leyrat, B. [1 ,2 ]
Guillemin, F. [1 ,2 ]
Lavielle, A. [7 ,8 ]
Cremillieux, Y. [8 ]
Seddik, K. [7 ]
Dufort, S. [7 ]
De Beaumont, O.
Thivat, E. [2 ,3 ,4 ]
Le Duc, G. [7 ]
机构
[1] Ctr Jean Perrin, Radiat Dept, F-63011 Clermont Ferrand, France
[2] Univ Clermont Auvergne, UFR Med, Clermont Ferrand, France
[3] Univ Clermont Auvergne, INSERM, U1240 IMoST, FR-63000 Clermont Ferrand, France
[4] Ctr Invest Clin UMR 501, F-63001 Clermont Ferrand, France
[5] Ctr Jean Perrin, Dept Clin Res Delegat Rech Clin & Innovat, F-63011 Clermont Ferrand, France
[6] Ctr Jean Perrin, Oncol Dept, F-63011 Clermont Ferrand, France
[7] NH TherAguix SA, Meylan, France
[8] Univ Bordeaux, Inst Sci Mol, UMR5255, Bordeaux, France
关键词
Glioblastoma; Radiotherapy; Nanoparticles; AGuIX; GADOLINIUM-BASED NANOPARTICLES; PLUS CONCOMITANT; BRAIN;
D O I
10.1016/j.ctro.2024.100833
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 mu M), and high (123-291 mu M) or very high (>291 mu M) 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 nano- particles 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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页数:7
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