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:Immunotherapy in non-small cell lung cancer: rationale, recent advances and future perspectives.
Immunotherapy in non-small cell lung cancer: rationale, recent advances and future perspectives.
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肺癌是全球第二大常见恶性肿瘤和癌症相关死亡的主要原因,其中非小细胞肺癌(NSCLC)是主要类型。以免疫检查点抑制剂(ICIs)为代表的免疫治疗是近年来包括NSCLC在内的实体瘤治疗的最大进展之一。然而,并非所有NSCLC患者都能在现有的程序性死亡配体1(PD-L1)和肿瘤突变负荷(TMB)选择标准下对免疫治疗产生有效应答。此外,相当一部分患者在免疫治疗过程中会出现非常规反应,包括假性进展或超进展疾病(HPD)、免疫相关毒性以及原发性或获得性耐药。为了更好地理解NSCLC中的免疫应答并为临床决策提供参考,本文综述了使用免疫治疗NSCLC的理论基础和最新进展。此外,我们还讨论了该方法当前面临的挑战和未来策略,以提高其治疗NSCLC的疗效和安全性。
Lung cancer, with non-small cell lung cancer (NSCLC) being the major type, is the second most common malignancy and the leading cause of cancer-related death globally. Immunotherapy, represented by immune checkpoint inhibitors (ICIs), has been one of the greatest advances in recent years for the treatment of solid tumors including NSCLC.
However, not all NSCLC patients experience an effective response to immunotherapy with the established selection criteria of programmed death ligand 1 (PD-L1) and tumor mutational burden (TMB).
Furthermore, a considerable proportion of patients experience unconventional responses, including pseudoprogression or hyperprogressive disease (HPD), immune-related toxicities, and primary or acquired resistance during the immunotherapy process. To better understand the immune response in NSCLC and provide reference for clinical decision-making, we herein review the rationale and recent advances in using immunotherapy to treat NSCLC.
Moreover, we discuss the current challenges and future strategies of this approach to improve its efficacy and safety in treating NSCLC.
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