一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:New Strategies and Combinations to Improve Outcomes in Immunotherapy in Metastatic Non-Small-Cell Lung Cancer.
New Strategies and Combinations to Improve Outcomes in Immunotherapy in Metastatic Non-Small-Cell Lung Cancer.
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免疫检查点抑制剂已经改变了转移性非小细胞肺癌的治疗格局,显著改善了生存,并具有持久临床缓解的潜力。尽管在一部分患者中观察到了显著缓解,但对当前免疫检查点抑制剂的原发性和获得性耐药仍构成关键挑战。目前正在开发多种新型联合免疫治疗和过继性细胞治疗策略,以应对治疗耐药。这些策略的成功取决于合理的临床试验设计,以及对可变肿瘤免疫微环境(TIME)中支撑免疫治疗耐药的免疫机制的审慎考量。需要进一步研究以促进对TIME内这些复杂机制的更深入理解,这可能最终为恢复和增强有效的抗肿瘤免疫应答提供关键。本综述旨在介绍一些近期用于晚期非小细胞肺癌(NSCLC)的值得注意的联合免疫治疗和细胞治疗策略,并基于当前对抗肿瘤免疫应答和TIME内耐药机制的理解,阐述其使用依据。
Immune checkpoint inhibitors have transformed the treatment of metastatic non-small-cell lung cancer, yielding marked improvements in survival and the potential for durable clinical responses. Primary and acquired resistance to current immune checkpoint inhibitors constitute a key challenge despite the remarkable responses observed in a subset of patients.
Multiple novel combination immunotherapy and adoptive cell therapy strategies are presently being developed to address treatment resistance. The success of these strategies hinges upon rational clinical trial design as well as careful consideration of the immunologic mechanisms within the variable tumor immune microenvironment (TIME) which underpin resistance to immunotherapy.
Further research is needed to facilitate a deeper understanding of these complex mechanisms within the TIME, which may ultimately provide the key to restoring and enhancing an effective anti-tumor immune response. This review aims to provide an introduction to some of the recent and notable combination immunotherapy and cell therapy strategies used in advanced non-small-cell lung cancer (NSCLC), and the rationale for their use based on current understanding of the anti-tumor immune response and mechanisms of resistance within the TIME.
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