决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:What is on the Horizon Beyond Platinum and Immunotherapy for Patients With Advanced Non-Small Cell Lung Cancer Without Actionable Genomic Aberrations?
非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因。
非小细胞肺癌(NSCLC)仍是全球癌症相关死亡的首要原因。尽管靶向治疗和免疫治疗已改变了一线治疗格局,但大多数无可操作基因组变异(AGA)的患者将在初始治疗的第一年内出现疾病进展。在此,我们综述了针对无AGA的晚期NSCLC患者的关键临床试验、新兴策略、挑战及未满足的需求。多西他赛联合或不联合雷莫西尤单抗是含铂化疗和免疫治疗后进展患者的标准二线治疗。靶向治疗仅适用于具有特定AGA的患者。理解癌症免疫逃逸的标志性特征是在化疗免疫治疗之外开发新策略的关键。抗血管生成药物与免疫检查点抑制剂(ICIs)的联合在含铂治疗和ICI进展后显示出喜忧参半的结果。双特异性抗体,特别是ivonescimab,在这一领域显示出令人鼓舞的早期疗效。人工智能驱动的病理组学和影像组学工具可能有助于未来优化治疗选择。CAR-T 细胞疗法仍处于研究阶段。无AGA的晚期NSCLC患者在化疗免疫治疗后进展,治疗选择有限。特定抗体等新型疗法已显示出有前景的结果。未来的进展将取决于预测性生物标志物的开发以及对ICI耐药机制的理解,以指导药物研发。
Non-small cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. While targeted therapy and immunotherapy have transformed first-line management, most patients without actionable genomic alterations (AGAs) will experience disease progression within the first year of their initial treatment. Here, we review pivotal trials, emerging strategies, challenges, and unmet needs for patients with advanced NSCLC without AGAs. Docetaxel with or without ramucirumab is the standard second-line therapy for patients who have progressed after platinum-based chemotherapy and immunotherapy. Targeted therapy is only suitable for patients with specific AGAs. Understanding the hallmarks of cancer immune evasion is key to developing new strategies beyond chemoimmunotherapy. The combination of antiangiogenic agents with immune checkpoint inhibitors (ICIs) has shown mixed results after progression on platinum and ICI. Bispecific antibodies, particularly ivonescimab, have shown encouraging early efficacy in this space. Artificial intelligence-driven pathomics and radiomics tools may help to refine treatment selection in the future. Chimeric antigen receptor T-cell therapy remains investigational. Patients with advanced NSCLC without AGAs who progressed after chemoimmunotherapy have limited treatment options. Novel therapies such as specific antibodies have shown promising results. Future progress will depend on the development of predictive biomarkers and understanding the mechanisms of resistance to ICIs to guide drug development.
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