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:Prognostic Significance of CD4+ Tumour Infiltrating Lymphocytes in Patients with Non-Small Cell Lung Cancer Receiving PD-1/PD-L1 Inhibitors Therapy.
Prognostic Significance of CD4+ Tumour Infiltrating Lymphocytes in Patients with Non-Small Cell Lung Cancer Receiving PD-1/PD-L1 Inhibitors Therapy.
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CD4+TIL(肿瘤浸润淋巴细胞)(TILs)已被发现在抗肿瘤免疫中发挥显著作用。在本研究中,作者探讨了CD4+ TILs在接受PD-1/PD-L1抑制剂治疗的非小细胞肺癌(NSCLC)患者中的预测价值。作者检索了Cochrane、Embase、PubMed和Web of Science,截止日期为2023年11月。
本研究遵循系统评价和荟萃分析优先报告条目(PRISMA)的要求。数据采用Stata MP17.0软件进行分析。终点包括客观缓解率(ORR)、无进展生存期(PFS)和总生存期(OS)。最终共有13项研究符合纳入标准。研究结果显示,肿瘤组织中高水平的CD4+ TILs与NSCLC患者更好的ORR相关(OR = 1.78,95% CI:1.15-2.76,p = 0.010),而与PFS(HR = 0.82,95% CI:0.65-1.05,p = 0.11)和OS(HR = 0.86,95% CI:0.69-1.09,p = 0.217)无关。
此外,外周血CD4+ T细胞高水平与更好的PFS相关(HR = 0.66,95% CI:0.46-0.94,p = 0.02),而与OS无关(HR = 0.90,95% CI:0.69-1.19,p = 0.461)。
结果表明,肿瘤组织中高CD4+ TILs可预测接受PD-1/PD-L1抑制剂的NSCLC患者更好的ORR,外周血高CD4+ T细胞可预测更好的PFS。关键词:CD4阳性T淋巴细胞,免疫检查点抑制剂,非小细胞肺癌,外周血,预后,肿瘤浸润。
CD4+ tumour infiltrating lymphocytes (TILs) have been found to produce a marked effect in anti-tumour immunity. In the present study, the authors explored the predictive value of CD4+ TILs in patients with non-small cell lung cancer (NSCLC) receiving PD-1/PD-L1 inhibitors therapy. The authors searched Cochrane, Embase, PubMed, and the Web of Science with a November 2023 deadline.
This study followed the requirements of the preferred reporting items for systematic reviews and meta-analyses (PRISMA). The data were analysed by Stata MP17. 0 software. Endpoints included objective response rate (ORR), progression-free survival (PFS), and overall survival (OS).
In total, 13 studies ultimately met the inclusion criteria. Findings showed high levels of CD4+ TILs in tumour tissue were correlated with better ORR (OR = 1. 78, 95% CI: 1. 15-2. 76, p = 0. 010) in NSCLC patients, rather than PFS (HR = 0. 82, 95% CI: 0. 65-1. 05, p = 0. 11) and OS (HR = 0. 86, 95% CI: 0. 69-1. 09, p = 0. 217).
In addition, high levels of peripheral blood CD4+ T cells correlated with better PFS (HR = 0. 66, 95% CI: 0. 46-0. 94, p = 0. 02), rather than OS (HR = 0. 90, 95% CI: 0. 69-1. 19, p = 0. 461). The results demonstrated that high CD4+ TILs in tumour tissue can predict better ORR for NSCLC patients receiving PD-1/PD-L1 inhibitors, and high peripheral blood CD4+ T cells can predict better PFS. Key Words: CD4-positive T-lymphocytes, Immune checkpoint inhibitors, Non-small cell lung cancer, Peripheral blood, Prognosis, Tumour-infiltrating.
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