不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The predictive implication of programmed cell death ligand 1 expression in extranodal natural killer/T-Cell lymphoma and its correlation with clinicopathological features: a systematic review and meta-analysis.
The predictive implication of programmed cell death ligand 1 expression in extranodal natural killer/T-Cell lymphoma and its correlation with clinicopathological features: a systematic review and meta-analysis.
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ENKTL 患者中 PD-L1 阳性表达与有利的临床特征相关。因此,PD-L1 阳性表达似乎是治疗获益的潜在预测因子。需要更多大规模、高质量的研究来进一步探索其预测价值。
尽管程序性细胞死亡配体1(PD-L1)在血液系统恶性肿瘤中的表达和功能已引起广泛关注,但其对结外自然杀伤/T细胞淋巴瘤(ENKTL)的预后价值仍不清楚。因此,我们进行了这项meta分析,以探讨肿瘤性PD-L1表达对ENKTL的预测价值。
检索了PubMed、Embase、Web of Science和CNKI数据库,以确定报告ENKTL患者PD-L1表达和生存结局的合格观察性研究。检索按照流行病学观察性研究Meta分析(MOOSE)指南进行。采用合并风险比(HRs)和95%置信区间(95% CIs)分析生存结局,采用比值比(ORs)和95% CIs分析临床病理参数。使用Review Manager 5.3和STATA 17.0进行统计分析。通过漏斗图和Egger检验评估潜在的发表偏倚。
共纳入7项研究中的433例ENKTL患者。汇总结果显示,肿瘤PD-L1表达与总生存期(OS)之间无显著关系(HR=1.35,95% CI:0.49-3.75,P=0.559)。我们还进行了亚组分析。然而,PD-L1表达升高与0-1分的低国际预后指数(IPI)评分相关(OR=2.46;95% CI:1.11-5.45,P=0.03)、良好的体能状态相关(OR=1.97;95% CI:1.11-3.51,P=0.02),以及良好的治疗效果相关(OR=2.61;95% CI:1.01-6.70,P=0.05)。
Although programmed cell death ligand 1 (PD-L1) expression and function in hematologic malignancies have aroused extensive attention, its prognostic value for extranodal natural killer/T-cell lymphoma (ENKTL) is still unknown. Therefore, we conducted this meta-analysis to explore the predictive value of neoplastic PD-L1 expression for ENKTL.
The PubMed, Embase, Web of Science, and CNKI databases were searched to identify eligible observational studies reporting PD-L1 expression and survival outcomes of ENKTL patients. The search was conducted in accordance with the Meta-analyses Of Observative Studies in Epidemiology (MOOSE) guidelines. The pooled hazard ratios (HRs) and 95% confidence intervals (95% CIs) were adopted to analyze survival outcomes, and the odds ratios (ORs) and 95% CIs were adopted for clinicopathological parameters. Review Manager 5.3 and STATA 17.0 were used for statistical analysis. Potential publication bias was evaluated by funnel plot and Egger's test.
A total of 433 patients with ENKTL were included across seven studies. The pooled results showed no significant relationship between neoplastic PD-L1 expression and overall survival (OS) (HR =1.35, 95% CI: 0.49-3.75, P=0.559). We also performed subgroup analyses. However, increased PD-L1 expression was associated with a low international prognostic index (IPI) score of 0-1 (OR =2.46; 95% CI: 1.11-5.45, P=0.03), good performance status (OR =1.97; 95% CI: 1.11-3.51, P=0.02), and a good treatment effect (OR =2.61; 95% CI: 1.01-6.70, P=0.05).
PD-L1-positive expression in patients with ENKTL was correlated with favorable clinical features. Thus, PD-L1-positive expression appears to be a potential predictor of treatment benefits. Additional large-scale, high-quality studies are needed to further explore its predictive value.
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