Medical Sciences Division, University of Oxford, Oxford, UK.
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Cancer Med. 2021 Sep;10(17):5983-5997. doi: 10.1002/cam4.4143. Epub 2021 Jul 26.
Inflammation is a hallmark of cancer, and systemic markers of inflammation are increasingly recognised as negative prognostic factors for clinical outcome. Neutrophil-to-lymphocyte ratio (NLR) is readily available from routine blood testing of patients diagnosed with cancer.
Peer-reviewed publications from PubMed/MEDLINE, Web of Science and EMBASE were identified according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. Hazard ratios (HR) for overall survival (OS) and surrogate endpoints (SE; comprising disease-, recurrence- and progression-free survival) were pooled using a random effects model. Additional analysis was carried out to further investigate NLR as an independent prognostic factor and account for heterogeneity.
Seventy-one eligible papers comprising 32,788 patients were identified. High NLR was associated with poor clinical outcomes. Significant publication bias was observed, and larger studies also adjusted for more covariates. Correcting for publication bias in multivariate studies brought our best estimate for true effect size to HR = 1.57 (95% CI 1.39-1.78; p < 0.0001) for OS and to HR = 1.38 (95% CI 1.16-1.64; p = 0.0003) for SE.
NLR is confirmed as an easily available prognostic biomarker in colorectal cancer, despite the limitations of some studies previously reporting this finding. As such, it should be routinely collected in prospective clinical trials. While more standardised and rigorous large-scale studies are needed before high NLR can be fully assessed as an independent predictor of CRC progression and outcome, the data suggest that it may be used to highlight individuals with tumour-promoting inflammatory context.
炎症是癌症的一个标志,越来越多的全身性炎症标志物被认为是临床预后的负面预测因素。中性粒细胞与淋巴细胞比值(NLR)可通过对诊断为癌症的患者进行常规血液检测获得。
根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,从 PubMed/MEDLINE、Web of Science 和 EMBASE 中确定经过同行评审的出版物。使用随机效应模型汇总总生存期(OS)和替代终点(包括疾病、复发和无进展生存期)的风险比(HR)。进行了额外的分析,以进一步研究 NLR 作为独立的预后因素并解释异质性。
确定了 71 篇符合条件的论文,共包含 32788 名患者。高 NLR 与较差的临床结局相关。观察到显著的发表偏倚,较大的研究也调整了更多的协变量。在多变量研究中纠正发表偏倚后,我们对真实效应大小的最佳估计值为 HR=1.57(95%CI 1.39-1.78;p<0.0001)用于 OS 和 HR=1.38(95%CI 1.16-1.64;p=0.0003)用于 SE。
尽管之前有一些研究报告了这一发现,但 NLR 被确认为结直肠癌中一种易于获得的预后生物标志物。因此,它应该在前瞻性临床试验中常规收集。虽然需要更多标准化和严格的大规模研究才能充分评估高 NLR 作为 CRC 进展和结局的独立预测因素,但数据表明,它可以用于突出具有肿瘤促进炎症背景的个体。