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:Emerging trends in cell-based therapies: contemporary advances and ethical considerations in translational neurosurgical oncology.
Emerging trends in cell-based therapies: contemporary advances and ethical considerations in translational neurosurgical oncology.
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新兴的细胞疗法代表了神经外科肿瘤学领域一项有前景的进展,为高级别胶质瘤等具有挑战性的诊断提供了新的治疗可能性。传统治疗方式,包括手术切除、化疗和放疗,由于恶性脑肿瘤的高度浸润性和基因组异质性,其疗效有限。近期将分子分型和基因型特征整合到诊断和治疗框架中,标志着向个性化医疗的重要演变。基于干细胞的策略,尤其是神经干细胞和间充质干细胞,对病理组织表现出显著的趋向性,为靶向治疗递送和内在抗肿瘤效应提供了创新策略。与此同时,免疫治疗进展,特别是免疫检查点抑制剂(ICIs)、CAR-T 细胞(CAR-T 细胞)疗法和肿瘤疫苗技术,通过利用患者特异性免疫反应且全身毒性极小,显著改变了治疗范式。为了对这些治疗创新进行背景化分析,我们系统回顾并分析了自2022年以来启动的28项正在进行的胶质母细胞瘤临床试验,这些试验研究了基于细胞的策略。该数据集阐明了试验设计、细胞靶点和联合免疫治疗方案中的关键模式。尽管具有巨大的临床前景,但整合基于细胞的治疗和免疫治疗需要审慎的伦理考量和复杂的临床管理策略,尤其是在与传统疗法联合使用时。本综述批判性地评估了当代进展,重点介绍了新兴临床试验结果,探讨了新型疗法的伦理维度,并强调了持续转化研究的必要性,以完善神经外科肿瘤学中患者特异性治疗范式。
Emerging cell-based therapies represent a promising advancement in neurosurgical oncology, offering novel therapeutic possibilities for challenging diagnoses such as high-grade gliomas. Traditional treatment modalities, including surgical resection, chemotherapy, and radiotherapy, offer limited efficacy due to the highly infiltrative nature and genomic heterogeneity of malignant brain tumors. The recent integration of molecular profiling and genotypic characterization into diagnostic and therapeutic frameworks underscores a significant evolution toward personalized medicine. Stem-cell-based approaches, notably neural and mesenchymal stem cells, demonstrate remarkable tropism for pathological tissues, providing innovative strategies for targeted therapeutic delivery and intrinsic anti-tumoral effects. Concurrently, immunotherapeutic advancements, particularly immune checkpoint inhibitors (ICIs), chimeric antigen receptor T-cell (CAR T-cell) therapies, and tumor vaccination techniques, have significantly altered therapeutic paradigms by leveraging patient-specific immune responses with minimal systemic toxicity.
To contextualize such therapeutic innovations, we systematically reviewed and analyzed 28 ongoing glioblastoma clinical trials initiated since 2022 investigating cell-based strategies. This dataset elucidates key patterns in trial design, cellular targets, and combinatorial immunotherapeutic regimens. Despite the immense clinical promise, integrating cell-based and immunological therapeutics necessitates careful ethical deliberation and complex clinical management strategies, particularly when combined with conventional therapies.
This review critically evaluates contemporary advancements, highlights emerging clinical trial outcomes, explores the ethical dimensions of novel therapeutics, and underscores the imperative for continued translational research to refine patient-specific therapeutic paradigms in neurosurgical oncology.
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