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癌症神经科学临床试验设计的新方法。

Novel approaches to clinical trial design in cancer neuroscience.

作者信息

Jones Gregory, Anderson Jennifer L, Nguyen Phuong T T, Gleber-Netto Frederico O, Hwang William L, Puduvalli Vinay K, Monje Michelle, Amit Moran

机构信息

Experimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Neuron. 2025 Sep 3;113(17):2791-2813. doi: 10.1016/j.neuron.2025.08.015.

Abstract

The emerging field of cancer neuroscience has revealed profound bidirectional interactions between the nervous system and cancer cells, identifying novel therapeutic vulnerabilities across diverse malignancies. This review examines the unique challenges and strategies for translating these insights into effective therapies. We propose innovative approaches to overcome these barriers through drug repurposing, enhanced biomarker development, and optimized trial designs. Repurposing neuroactive drugs with established safety profiles offers an accelerated path to clinical impact, particularly for targeting glutamatergic, adrenergic, and neurotrophic signaling pathways. Emphasizing mitigation of neurotoxicity and improved patient quality of life will be paramount moving forward. Repurposed agents that show preliminary potential for "dual use" (i.e., simultaneous toxicity mitigation and synergistic anti-tumor effects) are highlighted for special consideration. Master protocols and window-of-opportunity trials provide platforms to rapidly validate mechanisms while addressing patient-centered outcomes. By systematically addressing these foundational elements across disciplines, cancer neuroscience can translate its profound mechanistic insights into meaningful therapeutic advances for patients with treatment-resistant malignancies.

摘要

癌症神经科学这一新兴领域揭示了神经系统与癌细胞之间深刻的双向相互作用,确定了多种恶性肿瘤中全新的治疗靶点。本综述探讨了将这些见解转化为有效疗法所面临的独特挑战及策略。我们提出了创新方法,通过药物再利用、加强生物标志物开发和优化试验设计来克服这些障碍。重新利用具有既定安全特性的神经活性药物为产生临床影响提供了一条加速途径,特别是针对靶向谷氨酸能、肾上腺素能和神经营养信号通路。强调减轻神经毒性和改善患者生活质量在未来将至关重要。具有 “双重用途”(即同时减轻毒性和产生协同抗肿瘤作用)初步潜力的重新利用药物被特别强调以供特殊考虑。主方案和机会窗试验提供了平台,以便在解决以患者为中心的结果的同时迅速验证机制。通过系统地解决各学科的这些基础要素,癌症神经科学能够将其深刻的机制见解转化为对难治性恶性肿瘤患者有意义的治疗进展。

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