可溶性程序性细胞死亡配体-1 (sPD-L1)在外周t细胞淋巴瘤患者的预后和临床病理学价值:一项荟萃分析

IF 4.3
Annals of medicine Pub Date : 2025-12-01 Epub Date: 2025-02-10 DOI:10.1080/07853890.2025.2458236
Ying Wu, Yan Zhang
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引用次数: 0

摘要

背景:以往的研究探讨了可溶性程序性细胞死亡配体-1 (sPD-L1)能否预测外周t细胞淋巴瘤(PTCL)患者的预后;然而,没有得到一致的结果。因此,我们进行了本荟萃分析,以确定sPD-L1在预测PTCL预后中的确切意义。方法:检索PubMed、Embase、Web of Science和Cochrane Library,检索截止日期为2024年7月31日。结合危险比(hr)和95%可信区间(ci),检验sPD-L1对PTCL预后的预测价值。结果:共纳入7篇文章,共纳入445例患者。根据我们的汇总结果,PTCL患者sPD-L1升高与总生存期(OS)降低相关(HR = 4.22, 95%CI = 1.89-9.43, p = 0.004)。此外,较高的sPD-L1水平与男性(OR = 1.80, 95%CI = 1.06-3.03, p = 0.029)、国际预后指数(IPI)评分≥2 (OR = 4.32, 95%CI = 2.10-8.89, p p = 0.001)、存在B症状(OR = 2.56, 95%CI = 1.45-4.52, p = 0.001)、ECOG PS≥2 (OR = 7.41, 95%CI = 1.49-36.92, p = 0.015)相关。结论:根据本荟萃分析,PTCL患者较高的sPD-L1水平与较差的OS和较差的PFS显著相关。此外,高sPD-L1水平也与PTCL发展的临床特征相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prognostic and clinicopathological value of soluble programmed cell death ligand-1 (sPD-L1) in patients with peripheral T-cell lymphoma: a meta-analysis.

Prognostic and clinicopathological value of soluble programmed cell death ligand-1 (sPD-L1) in patients with peripheral T-cell lymphoma: a meta-analysis.

Prognostic and clinicopathological value of soluble programmed cell death ligand-1 (sPD-L1) in patients with peripheral T-cell lymphoma: a meta-analysis.

Prognostic and clinicopathological value of soluble programmed cell death ligand-1 (sPD-L1) in patients with peripheral T-cell lymphoma: a meta-analysis.

Background: Previous studies have explored whether soluble programmed cell death ligand-1 (sPD-L1) can be used to predict the prognosis of patients with peripheral T-cell lymphoma (PTCL); however, no consistent results have been obtained. Consequently, we conducted the present meta-analysis to identify the precise significance of sPD-L1 in predicting the prognosis of PTCL.

Methods: We searched PubMed, Embase, Web of Science, and the Cochrane Library until July 31, 2024. The value of sPD-L1 in predicting PTCL prognosis was examined by combining the hazard ratios (HRs) with 95% confidence intervals (CIs).

Results: Seven articles involving 445 patients were included in this study. Based on our pooled findings, increased sPD-L1 was associated with dismal overall survival (OS) (HR = 4.22, 95%CI = 1.89-9.43, p < 0.001) and worse progression-free survival (PFS) (HR = 2.57, 95%CI = 1.35-4.90, p = 0.004) in PTCL. Furthermore, higher sPD-L1 levels were correlated with male sex (OR = 1.80, 95%CI = 1.06-3.03, p = 0.029), International Prognostic Index (IPI) score ≥2 (OR = 4.32, 95%CI = 2.10-8.89, p < 0.001), elevated lactate dehydrogenase (LDH) level (OR = 5.15, 95%CI = 1.94-13.71, p = 0.001), presence of B symptoms (OR = 2.56, 95%CI = 1.45-4.52, p = 0.001), and ECOG PS ≥2 (OR = 7.41, 95%CI = 1.49-36.92, p = 0.015) in PTCL.

Conclusion: According to the present meta-analysis, higher sPD-L1 levels were significantly correlated with poor OS and inferior PFS in patients with PTCL. Additionally, high sPD-L1 levels were also associated with clinical features representing the development of PTCL.

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