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:The association between CD8+ tumor-infiltrating lymphocytes and the clinical outcome of cancer immunotherapy: A systematic review and meta-analysis.
The association between CD8+ tumor-infiltrating lymphocytes and the clinical outcome of cancer immunotherapy: A systematic review and meta-analysis.
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解读:我们的结果表明,高水平的肿瘤内、间质或侵袭性边缘 CD8+ T 细胞,而非循环 CD8+ T 细胞,可以预测接受 ICIs 治疗的不同癌症患者的治疗结局,无论是单药 ICIs 还是与其他疗法联合。
癌症患者对免疫检查点抑制剂(ICIs)的反应成功率各不相同。CD8+ TIL(肿瘤浸润淋巴细胞)(TILs)在杀伤肿瘤细胞中发挥关键作用。本研究旨在评估 CD8+ TILs 在接受 ICIs 治疗的癌症患者中的预后作用。
我们系统检索了截至2021年7月12日PubMed、EMBASE和Cochrane Library中的所有出版物,不限语言或文章类型。纳入评估高CD8+ TILs与低CD8+ TILs在预测各种癌症患者疗效和生存方面作用的研究。结局包括总生存期(OS)、无进展生存期(PFS)和客观缓解率(ORR)。研究方案已在PROSPERO前瞻性注册(注册号CRD42021233654)。
结果:共纳入33项研究,包含2559例癌症患者。结果显示,在接受ICIs治疗的患者中,高CD8+ TILs与更好的OS(HR,0.52;95% confidence interval:0.41-0.67;p < 0.001)、PFS(HR,0.52;95% confidence interval:0.40-0.67;p < 0.001)和ORR(OR,4.08;95% confidence interval:2.73-6.10;p < 0.001)显著相关。亚组分析提示,无论治疗方案不同(ICI单药治疗或联合治疗)、癌症类型不同(NSCLC、黑色素瘤及其他),以及CD8+ T细胞位置不同(瘤内、间质和浸润边缘),高CD8+ TILs患者均具有更好的临床获益。与低基线相比,外周血中较高的基线循环CD8+ T细胞并未有助于改善OS(HR,0.93;95% confidence interval:0.67-1.29;p = 0.67)和PFS(HR,0.89;95% confidence interval:0.60-1.32;p = 0.56)。
The responses of cancer patients to immune checkpoint inhibitors (ICIs) vary in success. CD8+ tumor infiltrating lymphocytes (TILs) play a key role in killing tumor cells. This study aims to evaluate the prognostic role of CD8+ TILs in cancer patients treated with ICIs.
We systematically searched all publications from PubMed, EMBASE, and Cochrane Library until 12 Jul 2021 without any restriction of language or article types. Studies assessing high versus low CD8+ TILs in predicting efficacy and survival of various cancer patients were included. The outcomes included overall survival (OS), progression-free survival (PFS), and objective response rate (ORR). The study protocol is prospectively registered on PROSPERO (registration number CRD42021233654).
Findings: A total of 33 studies consisting of 2559 cancer patients were included. The result showed that high CD8+ TILs were significantly associated with better OS (HR, 0.52; 95% confidence interval: 0.41-0.67; p < 0.001), PFS (HR, 0.52; 95% confidence interval: 0.40-0.67; p < 0.001) and ORR (OR, 4.08; 95% confidence interval: 2.73-6.10; p < 0.001) in patients treated with ICIs. Subgroup analyses suggested that patients with high CD8+ TILs had a better clinical benefit, regardless of different treatments (ICI mono therapy, or combination therapy), cancer types (NSCLC, melanoma and others), and CD8+ T cells locations (intra-tumor, stroma, and invasive margin). The higher baseline circulating CD8+ T cells from peripheral blood did not contribute to the improved OS (HR, 0.93; 95% confidence interval: 0.67-1.29; p = 0.67) and PFS (HR, 0.89; 95% confidence interval: 0.60-1.32; p = 0.56) compared with the low baseline. INTERPRETATION: Interpretation: Our results suggested that high intra-tumoral, stromal, or invasive marginal, but not circulating CD8+ T cells, can predict treatment outcomes in patients with ICIs therapy across different cancers, in either single-agent ICIs or combination with other therapies. FUNDING: Funding: China National Science Foundation (Grant No. 82,022,048, 81,871,893), Key Project of Guangzhou Scientific Research Project (Grant No. 201,804,020,030), High-level university construction project of Guangzhou medical university (Grant No. 20,182,737, 201,721,007, 201,715,907, 2,017,160,107); National key R & D Program (Grant No. 2017YFC0907903 & 2017YFC0112704) and the Guangdong high level hospital construction "reaching peak" plan.
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