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胶质母细胞瘤治疗中靶向α疗法的现状与未来方向

Current landscape and future directions of targeted-alpha-therapy for glioblastoma treatment.

作者信息

Roncali Loris, Hindré François, Samarut Edouard, Lacoeuille Franck, Rousseau Audrey, Lemée Jean-Michel, Garcion Emmanuel, Chérel Michel

机构信息

Centre for Research in Molecular Medicine and Chronic Diseases (CiMUS), University of Santiago de Compostela; E-15782 Santiago de Compostela, Spain.

University of Angers, INSERM, CNRS, CRCI 2 NA; F-49000 Angers, France.

出版信息

Theranostics. 2025 Mar 31;15(11):4861-4889. doi: 10.7150/thno.106081. eCollection 2025.

DOI:10.7150/thno.106081
PMID:40303349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12036880/
Abstract

Glioblastoma (GB) is the most aggressive malignancy of the central nervous system. Despite two decades of intensive research since the establishment of the standard of care, emerging strategies have yet to produce consistent satisfactory outcomes. Because of its specific localisation and intricate characteristics, GB is a uniquely regulated solid tumour with a strong resistance to therapy. Advances in targeted radionuclide therapy (TRT), particularly with the introduction of a-emitting radionuclides, have unveiled potential avenues for the management of GB. Recent preclinical and clinical studies underscored promising advancements for targeted-α-therapy (TAT), but these therapeutic approaches exhibit a vast design heterogeneity, encompassing diverse radionuclides, vectors, target molecules, and administration modalities. This review seeks to critically assess the therapeutic landscape of GB through the perspective of TAT. Here, the focus is made on the advancements and limitations of explorations, pilot studies, and clinical trials, to determine the best directions for future investigations. In doing so, we hope to identify existing challenges and draw insights that might pave the way towards a more effective therapeutic approach.

摘要

胶质母细胞瘤(GB)是中枢神经系统最具侵袭性的恶性肿瘤。尽管自确立治疗标准以来经过了二十年的深入研究,但新出现的策略尚未产生一致令人满意的结果。由于其特殊的定位和复杂的特征,GB是一种独特调控的实体瘤,对治疗具有很强的抗性。靶向放射性核素治疗(TRT)的进展,特别是随着发射α粒子的放射性核素的引入,为GB的治疗揭示了潜在途径。最近的临床前和临床研究强调了靶向α治疗(TAT)的有前景的进展,但这些治疗方法表现出巨大的设计异质性,包括不同的放射性核素、载体、靶分子和给药方式。本综述旨在通过TAT的视角批判性地评估GB的治疗前景。在此,重点关注探索性研究、试点研究和临床试验的进展与局限性,以确定未来研究的最佳方向。通过这样做,我们希望识别现有挑战并获得可能为更有效的治疗方法铺平道路的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ff/12036880/d1676d19b2ea/thnov15p4861g008.jpg
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