The evolution of chemotherapy in brain tumors: from historical milestones to precision medicine in glioblastoma.

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2026-05-21 eCollection Date: 2026-01-01 DOI:10.37349/etat.2026.1002374
Alessia Ciafarone, Paola Palumbo
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引用次数: 0

Abstract

Chemotherapy has profoundly shaped modern oncology, evolving from early cytotoxic approaches to biologically informed strategies. In glioblastoma (GBM), the highly aggressive primary brain tumor, precision medicine does not rely on the identification of a single crucial oncogenic driver but integrates biologically informed stratification strategies to predict treatment response, resistance, and therapy-induced adaptation. This review recapitulates the historical milestones of chemotherapeutic development in neuro-oncology, with particular emphasis on GBM. As the main chemotherapeutic agent currently used in GBM, temozolomide (TMZ) initially represented a major therapeutic breakthrough; however, its clinical use has progressively unveiled the biological and clinical limitations of conventional cytotoxic paradigms. While TMZ exerts antitumor activity through DNA damage-induced apoptosis, accumulating experimental evidence indicates that it may also elicit adaptive responses, ultimately supporting tumor progression and therapy resistance. By integrating historical milestones with recent molecular understanding, this review highlights how improved knowledge of therapy-induced adaptations may inform emerging precision medicine strategies in GBM, underscoring the need for tailored treatments to overcome tumor heterogeneity and adaptive responses.

脑肿瘤化疗的演变:从历史里程碑到胶质母细胞瘤的精准医学。
化疗深刻地塑造了现代肿瘤学,从早期的细胞毒性方法发展到生物学知情的策略。在胶质母细胞瘤(GBM)这种高度侵袭性的原发性脑肿瘤中,精准医学不依赖于识别单一的关键致癌驱动因素,而是整合生物学信息分层策略来预测治疗反应、耐药性和治疗诱导的适应。这篇综述概述了神经肿瘤学化疗发展的历史里程碑,特别强调了GBM。作为目前用于GBM的主要化疗药物,替莫唑胺(TMZ)最初代表了一项重大的治疗突破;然而,它的临床应用逐渐揭示了传统细胞毒性范式的生物学和临床局限性。虽然TMZ通过DNA损伤诱导的细胞凋亡发挥抗肿瘤活性,但越来越多的实验证据表明,TMZ也可能引发适应性反应,最终支持肿瘤进展和治疗耐药性。通过整合历史里程碑和最近的分子理解,本综述强调了治疗诱导的适应知识的改进如何为GBM的新兴精准医学策略提供信息,强调了定制治疗以克服肿瘤异质性和适应性反应的必要性。
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
2.80
自引率
0.00%
发文量
0
审稿时长
13 weeks
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