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复发性高级别脑膜瘤药物治疗进展

英文原题:Advances in Pharmacological Therapy for Recurrent High-Grade Meningiomas.

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Advances in Pharmacological Therapy for Recurrent High-Grade Meningiomas.

PubMed 2026/07/24(内容时间) Curr Cancer Drug Targets Q3 · IF 2.5(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

传统细胞毒性化疗在复发性高级别脑膜瘤中显示的生存获益有限,主要用于姑息性症状管理。

研究思路结论见上方概要

世界卫生组织(WHO)2级和3级脑膜瘤是侵袭性肿瘤,以术后高复发率和不良预后为特征。尽管手术和放射治疗管理取得了进展,但复发性WHO 2/3级脑膜瘤的有效全身治疗选择仍然有限,大多数疗法仍处于临床研究阶段。

评估复发高级别脑膜瘤各种药物治疗策略的疗效和安全性,包括传统化疗、靶向治疗和免疫治疗。

在PubMed、Embase、Web of Science和ClinicalTrials.gov中进行了全面的文献检索,检索时间从数据库建库至2025年8月。系统综述了探讨复发高级别脑膜瘤常规化疗、靶向治疗和免疫治疗的相关研究,以总结精准治疗策略的当前进展。

展开英文摘要原文

To evaluate the efficacy and safety of various pharmacological treatment strategies for recurrent high-grade meningioma, including conventional chemotherapy, targeted therapy, and immunotherapy.

A comprehensive literature search was conducted in PubMed, Embase, Web of Science, and ClinicalTrials.gov from database inception to August 2025. Relevant studies investigating conventional chemotherapy, targeted therapy, and immunotherapy for recurrent high-grade meningioma were systematically reviewed to summarize current advances in precision therapeutic strategies. DISCUSSION: Conventional cytotoxic chemotherapy has demonstrated limited survival benefit in recurrent high-grade meningioma and is primarily used for palliative symptom management. In contrast, molecular targeted therapies have shown varying degrees of anti-tumor activity, including anti-angiogenic agents, Tyrosine Kinase Inhibitors (TKI), Focal Adhesion Kinase (FAK) inhibitors, and Mammalian Target of Rapamycin (mTOR) inhibitors. Among these, Bevacizumab demonstrated relatively favorable efficacy, prolonging median progression-free survival to 12-18 months in phase II clinical studies. Immunotherapy has also emerged as a promising therapeutic approach. Programmed death-1 (PD-1) inhibitors achieved 6-month progression-free survival rates (PFS-6) of up to 48% in early clinical studies. Furthermore, emerging immunotherapeutic strategies, such as chimeric antigen receptor T-cell (CAR-T) therapy, oncolytic virus (OVs) therapy, and personalized tumor vaccines, have demonstrated preliminary therapeutic potential. Nevertheless, developing standardized treatment strategies remains challenging due to limited clinical trial sample sizes, methodological heterogeneity, and substantial intertumoral and intratumoral molecular variability.

Future research should prioritize molecular subtype-based therapeutic strategies to facilitate personalized treatment according to tumor biology. In addition, combination regimens integrating targeted therapy and immunotherapy may further improve therapeutic response and quality of life in patients with recurrent high-grade meningioma.

论文信息

作者
Bai R、Yin S、Wang Y、Zhang Y、Li W、Chen F
单位
Department of Neuro-Oncology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.China
期刊
Current cancer drug targets2026 Jul 24
原文标识
PubMed 42517405 · DOI 10.2174/0115680096470037260713093535