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:Association between CD8+ tumor-infiltrating lymphocytes and prognosis of non-small cell lung cancer patients treated with PD-1/PD-L1 inhibitors: a systematic review and meta-analysis.
Association between CD8+ tumor-infiltrating lymphocytes and prognosis of non-small cell lung cancer patients treated with PD-1/PD-L1 inhibitors: a systematic review and meta-analysis.
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尽管 CD8+ TILs 的位置不同,高密度的 CD8+ TILs 仍可预测接受 PD-1/PD-L1 抑制剂治疗的 NSCLC 患者的治疗结局。
本荟萃分析旨在研究PD-1/PD-L1抑制剂治疗的非小细胞肺癌(NSCLC)患者中,CD8⁺TIL(肿瘤浸润淋巴细胞)的预后价值。
检索PubMed、Embase、Web of Science和Cochrane Library数据库,检索截至2023年2月7日。纳入研究CD8⁺ TIL与PD-1/PD-L1抑制剂治疗NSCLC疗效关系的临床研究。使用RevMan 5.3和StataMP 17.0进行荟萃分析,结局指标包括总生存期(OS)、无进展生存期(PFS)和客观缓解率(ORR)。
共纳入19篇文章、1488例患者。分析结果显示,PD-1/PD-L1抑制剂治疗的NSCLC患者中,CD8⁺ TIL水平较高与更好的OS(HR=.60;95% CI .46–.77;P<.0001)、PFS(HR=.68;95% CI .53–.88;P=.003)及ORR(OR=2.26;95% CI 1.52–3.36;P<.0001)相关。亚组分析显示,无论CD8⁺ TIL位于肿瘤内还是基质中,水平较高患者均有较好的临床预后获益;与东亚人群相比,白人中CD8⁺ TIL水平较高与更好的预后相关。接受PD-1/PD-L1抑制剂的NSCLC患者中,外周血CD8⁺ TIL水平较高并未改善OS(HR=.83;95% CI .69–1.01;P=.06)或PFS(HR=.93;95% CI .61–1.14;P=.76)。
无论CD8⁺ TIL的位置如何,其密度较高均可预测接受PD-1/PD-L1抑制剂治疗NSCLC患者的结局。但外周血中CD8⁺ TIL水平较高不具预测作用。
A meta-analysis method was used to investigate the prognostic value of CD8+ tumor-infiltrating lymphocytes (TILs) in non-small cell lung cancer (NSCLC) patients treated with PD-1/PD-L1 inhibitors.
A database search of PubMed, Embase, Web of Science and Cochrane Library up until 7 February, 2023. A clinical study on the relationship between CD8+ TILs and PD-1/PD-L1 inhibitors in the therapeutics of NSCLC. RevMan 5.3 and StataMP 17.0 software were used for meta-analysis. The outcome indicators incorporated overall survival (OS), progression-free survival (PFS) and objective response rate (ORR).
Nineteen articles with 1488 patients were included. The analysis results showed that high CD8+ TILs were associated with better OS (HR = 0.60, 95% CI: 0.46-0.77; P < 0.0001), PFS (HR = 0.68, 95% CI: 0.53-0.88; P = 0.003) and ORR (OR = 2.26, 95% CI: 1.52-3.36; P < 0.0001) in NSCLC patients treated with PD-1/PD-L1 inhibitors. Subgroup analysis indicated that patients with high CD8+ TILs had good clinical prognostic benefits whether the location of CD8+ TILs was intratumoral or stromal, and compared with East Asian, high CD8+ TILs in Caucasians showed a better prognosis. High CD8+ TILs in peripheral blood did not improve OS (HR = 0.83, 95% CI: 0.69-1.01; P = 0.06) and PFS (HR = 0.93, 95% CI: 0.61-1.14; P = 0.76) in NSCLC patients receiving PD-1/PD-L1 inhibitors.
In spite of the location of CD8+ TILs, high densities of CD8+ TILs were predictive of treatment outcomes in NSCLC patients treated with PD-1/PD-L1 inhibitors. However, high CD8+ TILs in peripheral blood had no predictive effect.
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