Exploring the landscape of targetable alterations in patients with glioblastoma

IF 94.6 1区 医学 Q1 ONCOLOGY
Elisa Aquilanti, Mehdi Touat, Pim French, Antonio Iavarone, David Capper, Marjolein Geurts, Rifaquat Rahman, Roel Verhaak, Matthias Preusser, Martin van den Bent, Patrick Y. Wen
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Abstract

Glioblastomas remain the most lethal primary brain tumour in adults, with targeted therapies delivering only limited benefit despite deep molecular characterization. Several targeted drugs have received regulatory approval for low-grade gliomas, although progress in glioblastomas remains constrained by, among other aspects, extensive intratumoural heterogeneity, pathway redundancy, cellular plasticity and limited drug delivery to the central nervous system. Some of these challenges might be mitigated through strategies that enhance blood–brain penetration, including focused ultrasonography, convection-enhanced delivery, efflux avoidance and chemical modifications. Improved tumour profiling through multiregional sampling, prioritization of truncal dependencies and the development of novel therapeutic modalities, such as antibody–drug conjugates and theranostics, might also further improve outcomes. In this Review, we summarize the therapeutic landscape of targeted therapies in glioblastomas, spanning major target classes including receptor tyrosine kinases, intracellular signalling proteins, cell-cycle dysregulation and synthetic-lethal vulnerabilities. We also examine emerging strategies targeting genome integrity and telomeres, epigenetic modulators, and tumour–neural circuitry. Furthermore, we highlight tumour heterogeneity and extrachromosomal DNA dynamics as key drivers of oncogene amplification and therapeutic resistance as well as the roles of novel clinical trial designs and liquid biopsy-based monitoring strategies. Lastly, we discuss pathway-based glioblastoma classification and master kinase mapping as methods for aligning drugs with functional tumour states. Despite considerable progress in other cancer types, progress with the development of targeted therapies for patients with glioblastoma has remained limited, despite considerable research effort. In this Review, the authors summarize the various attempts to develop effective targeted therapies for patients with glioblastoma, including some of the challenges that have likely impaired progress thus far. The authors also highlight novel therapies, clinical trial designs and research directions that have been informed by the shortcomings of previous research efforts, all of which might eventually lead to improved outcomes for patients.
探索胶质母细胞瘤患者可靶向改变的前景。
胶质母细胞瘤仍然是成人中最致命的原发性脑肿瘤,尽管有深入的分子特征,但靶向治疗只能提供有限的益处。几种靶向药物已经获得了低级别胶质瘤的监管批准,尽管胶质母细胞瘤的进展仍然受到肿瘤内广泛的异质性、通路冗余、细胞可塑性和中枢神经系统药物递送有限等方面的限制。其中一些挑战可以通过增强血脑穿透的策略来缓解,包括聚焦超声、对流增强输送、避免外排和化学修饰。通过多区域采样改进肿瘤谱,对截断依赖性进行优先排序以及开发新的治疗方式,如抗体-药物偶联物和治疗学,也可能进一步改善结果。在这篇综述中,我们总结了胶质母细胞瘤靶向治疗的治疗前景,包括受体酪氨酸激酶、细胞内信号蛋白、细胞周期失调和合成致死脆弱性等主要靶点。我们还研究了针对基因组完整性和端粒、表观遗传调节剂和肿瘤神经回路的新兴策略。此外,我们强调肿瘤异质性和染色体外DNA动力学是癌基因扩增和治疗耐药性的关键驱动因素,以及新型临床试验设计和基于液体活检的监测策略的作用。最后,我们讨论了基于途径的胶质母细胞瘤分类和主激酶定位作为将药物与功能肿瘤状态对齐的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
99.40
自引率
0.40%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Nature Reviews publishes clinical content authored by internationally renowned clinical academics and researchers, catering to readers in the medical sciences at postgraduate levels and beyond. Although targeted at practicing doctors, researchers, and academics within specific specialties, the aim is to ensure accessibility for readers across various medical disciplines. The journal features in-depth Reviews offering authoritative and current information, contextualizing topics within the history and development of a field. Perspectives, News & Views articles, and the Research Highlights section provide topical discussions, opinions, and filtered primary research from diverse medical journals.
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