CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Advanced Neuroimaging and Emerging Systemic Therapies in Glioblastoma: Current Evidence and Future Directions.
Advanced Neuroimaging and Emerging Systemic Therapies in Glioblastoma: Current Evidence and Future Directions.
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尽管技术进步,胶质母细胞瘤(GBM)的预后仍然极差。现代神经影像学方法在脑肿瘤的诊断和监测中发挥着越来越大的作用。本综述展示了当前胶质母细胞瘤的神经影像学方法和全身治疗策略,重点关注新兴和创新性治疗。多参数磁共振成像-MRI(扩散、灌注和波谱)以及新型正电子发射断层扫描(PET)示踪剂的进展,辅以影像组学和人工智能(AI),现已能够优化肿瘤勾画、区分进展与治疗效应,并可能有助于预测治疗反应。最大安全范围切除术后辅以替莫唑胺放化疗仍是标准方案,在O 6 -甲基鸟嘌呤DNA甲基转移酶(MGMT)启动子甲基化肿瘤中获益最大。贝伐珠单抗及其他靶向治疗方式主要提供无进展生存期获益,而非总生存期获益。免疫检查点抑制剂(如纳武利尤单抗)未能在未经选择的GBM中改善生存,而早期多抗原CAR-T(CAR-T 细胞)策略显示出初步生物活性,但持久性尚未确立。尽管可操作变异(NTRK融合和BRAF V600E)支持选择性靶向治疗试验,但其在经典GBM中的确切获益尚未得到证实。未来优先方向包括协调影像-分子整合、AI驱动的预后建模、新型PET示踪剂,以及突破或暂时开放血脑屏障以增强药物递送的策略。这些领域的融合可能将诊断精准度转化为患者预后的改善。
Despite technological progress, glioblastoma (GBM) continues to confer dismal prognoses. Modern neuroimaging methods are assuming an ever greater role in diagnosing and monitoring brain tumors. This review shows current neuroimaging approaches and systemic therapeutic strategies for glioblastoma, with a focus on emerging and innovative treatments. Advances in multiparametric magnetic resonance imaging-MRI (diffusion, perfusion, and spectroscopy) and novel positron emission tomography (PET) tracers, complemented by radiomics and artificial intelligence (AI), now refine tumor delineation, differentiate progression from treatment effects, and may help predict treatment responses. Maximal safe resection followed by chemoradiotherapy with temozolomide remains the standard, with the greatest benefit seen in O 6 -methylguanine DNA methyltransferase (MGMT) promoter-methylated tumors.
Bevacizumab and other targeted modalities offer mainly progression-free, not overall survival, gains. Immune checkpoint inhibitors (e. g. , nivolumab) have not improved survival in unselected GBM, while early multi-antigen CAR-T (chimeric antigen receptor T-cell) strategies show preliminary bioactivity without established durability.
While actionable alterations (NTRK fusions and BRAF V600E) justify selective targeted therapy trials, their definitive benefit in classical GBM is unproven. Future priorities include harmonized imaging molecular integration, AI-driven prognostic modeling, novel PET tracers, and strategies to breach or transiently open the blood-brain barrier to enhance drug delivery. Convergence of these domains may convert diagnostic precision into improved patient outcomes.
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