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:Overcoming Immunotherapy Resistance in Small-Cell Lung Cancer.
Overcoming Immunotherapy Resistance in Small-Cell Lung Cancer.
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小细胞肺癌(SCLC)是肺癌中最致命的组织学亚型。其特征为肿瘤快速生长和早期转移播散,导致预后极差。在标准化疗基础上加入免疫治疗使广泛期疾病患者的生存获得了适度改善。然而,由于对免疫治疗的原发性和获得性耐药,总体临床获益仍然有限。事实上,免疫检查点抑制剂的疗效受多种因素影响,包括肿瘤异质性、免疫抑制性肿瘤微环境以及该疾病固有的分子特征。近年来,已开展了积极的研究以识别并在治疗上克服免疫治疗耐药机制,越来越多的提示性证据正在为SCLC患者临床管理的新策略指明方向。在这篇综述文章中,我们总结并讨论了免疫治疗临床疗效面临的重大障碍,特别侧重于已发表和正在进行的临床试验,这些试验探讨了克服免疫治疗耐药机制的潜在策略。此外,我们报告并讨论了已测试的新治疗方法,尤其是抗体药物偶联物、双特异性抗体、过继性细胞疗法和联合策略的使用。
Small-cell lung cancer (SCLC) is the most lethal histologic subtype of lung cancer. It is characterized by rapid tumor growth and early metastatic dissemination, resulting in an extremely poor prognosis. The addition of immunotherapy to standard chemotherapy has led to a modest improvement in survival for patients with extensive-stage disease.
However, the overall clinical benefit remains limited due to both primary and acquired resistance to immunotherapy. Indeed, the efficacy of immune checkpoint inhibitors is influenced by multiple factors, including tumor heterogeneity, an immunosuppressive tumor microenvironment, and intrinsic molecular characteristics of the disease.
In recent years, active research has been conducted to identify and therapeutically overcome resistance mechanisms to immunotherapy, and accumulating suggestive evidence is lighting the way for new strategies for clinical management of patients with SCLC. In this review article, we summarize and discuss the substantial obstacle to immunotherapy clinical efficacy, with a particular emphasis on the published and ongoing clinical trials that investigated the potential strategies to overcome mechanisms of resistance to immunotherapy.
Moreover, we report and discuss the new therapeutic approaches tested, especially the use of antibody-drug conjugates, bi-specific antibodies, adoptive cell therapies and combination strategies.
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