A phase I study of convection-enhanced delivery (CED) of liposomal-irinotecan using real-time magnetic resonance imaging in patients with recurrent high-grade glioma.

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY Journal of Neuro-Oncology Pub Date : 2025-01-06 DOI:10.1007/s11060-024-04904-y
Kazim H Narsinh, Karishma Kumar, Krystof Bankiewicz, Alastair J Martin, Mitchell Berger, Jennifer Clarke, Jennie Taylor, Nancy Ann Oberheim Bush, Annette M Molinaro, Manish Aghi, Nicholas Butowski
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Abstract

Background: Irinotecan demonstrates anti-tumor efficacy in preclinical glioma models but clinical results are modest due to drug delivery limitations. Convection enhanced delivery (CED) improves drug delivery by increasing intratumoral drug concentration. Real-time magnetic resonance imaging of infusate delivery during CED may optimize tumor coverage. This phase 1 trial examines the safety and tolerability of liposomal irinotecan and gadolinium delivered via CED using real-time MRI guidance in recurrent high-grade glioma patients.

Methods: Initially, a 3 + 3 dose-escalating, single dose trial was planned with 4 cohorts based on a fixed drug dose and volume. After 9 patients, a protocol amendment allowed for variable volume and dose of the study agent based on tumor size. The amended design specified 'personalized' drug volume but fixed concentration of 20 mg/mL of liposomal irinotecan in the first cohort escalating to 40 mg/mL in the second cohort.

Results: Eighteen patients with recurrent WHO grade 3 or 4 gliomas (diameter 1-4 cm) were treated. Based on the tumor volume, the total dose of liposomal irinotecan was 20-680 mg in a total volume of 2-17 ml. Technical challenges were overcome by real-time MRI guidance and protocol amendment. The only dose-limiting toxicity (DLT) was a grade 3 stroke. Safety and survival information is presented.

Conclusions: CED of liposomal irinotecan using real-time MRI in patients with recurrent high-grade glioma is feasible. Image-guidance allowed for improved placement of CED cannulas and optimal tumor coverage. Our results warrant further study with repeat CED dosing.

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一项利用实时磁共振成像技术对复发性高级别胶质瘤患者进行对流增强输送(CED)脂质体伊立替康的I期研究。
背景:伊立替康在临床前神经胶质瘤模型中显示出抗肿瘤疗效,但由于药物递送的限制,临床结果并不理想。对流增强传递(CED)通过增加肿瘤内药物浓度来改善药物传递。实时磁共振成像灌注输注在CED期间可以优化肿瘤覆盖。该1期临床试验检验了伊立替康和钆脂质体在高级别胶质瘤复发患者中的安全性和耐受性。方法:最初,计划进行3 + 3剂量递增的单剂量试验,4个队列,基于固定的药物剂量和体积。在9例患者后,修改了一项方案,允许根据肿瘤大小改变研究药物的体积和剂量。修改后的设计指定了“个性化”药物体积,但在第一个队列中伊立替康脂质体的固定浓度为20mg /mL,在第二个队列中增加到40mg /mL。结果:18例WHO 3级或4级胶质瘤(直径1 ~ 4cm)复发患者接受治疗。根据肿瘤体积,伊立替康脂质体总剂量为20-680 mg,总体积为2-17 ml。通过实时MRI指导和方案修改,克服了技术难题。唯一的剂量限制性毒性(DLT)是3级中风。提供安全和生存信息。结论:实时MRI检测伊立替康脂质体在复发性高级别胶质瘤患者中的应用是可行的。图像引导可以改善CED套管的放置和最佳的肿瘤覆盖。我们的结果值得进一步研究重复给药。
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来源期刊
Journal of Neuro-Oncology
Journal of Neuro-Oncology 医学-临床神经学
CiteScore
6.60
自引率
7.70%
发文量
277
审稿时长
3.3 months
期刊介绍: The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.
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