Vairy Stephanie, Michaiel George
Division of Hematology-Oncology, Department of Pediatrics, Centre Hospitalier Universitaire de Sherbrooke, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Centre de Recherche du CHUS, Sherbrooke, QC J1H 5N4, Canada.
Curr Oncol. 2025 Jul 25;32(8):417. doi: 10.3390/curroncol32080417.
Advances in molecular diagnostics have enabled precision medicine approaches in pediatric neuro-oncology, with small-molecule drugs emerging as promising therapeutic candidates targeting specific genetic and epigenetic alterations in central nervous system (CNS) tumors. This review provides a focused overview of several small-molecule agents under investigation or in early clinical use, including ONC201, tazemetostat, vorasidenib, CDK inhibitors, selinexor, and aurora kinase A inhibitors, among others. Highlighted are their mechanisms of action, pharmacokinetic properties, early efficacy data, and tolerability in pediatric populations. Despite encouraging preclinical and early-phase results, most agents face limitations due to study heterogeneity, lack of large-scale pediatric randomized trials, and challenges in drug delivery to the CNS. The review underscores the critical need for robust prospective clinical trials for the integration of these therapies into pediatric neuro-oncology care.
分子诊断学的进展已使小儿神经肿瘤学能够采用精准医学方法,小分子药物作为针对中枢神经系统(CNS)肿瘤中特定基因和表观遗传改变的有前景的治疗候选药物而出现。本综述重点概述了几种正在研究或处于早期临床应用阶段的小分子药物,包括ONC201、他泽司他、伏立替尼、CDK抑制剂、塞利尼索和极光激酶A抑制剂等。重点介绍了它们在儿科人群中的作用机制、药代动力学特性、早期疗效数据和耐受性。尽管临床前和早期阶段的结果令人鼓舞,但由于研究的异质性、缺乏大规模儿科随机试验以及药物向中枢神经系统递送方面的挑战,大多数药物都面临局限性。该综述强调了开展强有力的前瞻性临床试验以将这些疗法纳入小儿神经肿瘤学治疗的迫切需求。