Prognostic value of neutrophil to lymphocyte ratio in patients with esophagus cancer receiving neoadjuvant therapy: a systematic review and meta-analysis.

IF 5.9 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2025-10-06 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1615962
Longwei Ma, Jiaxing He, Ping Li, Long Ma, He Wang, Yanchao Deng
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引用次数: 0

Abstract

Background: Growing research reveals a relation of the neutrophil-to-lymphocyte ratio (NLR) to clinical outcomes of the esophageal cancer (EC) population undergoing neoadjuvant therapy. However, current findings remain inconclusive and somewhat controversial.

Methods: PubMed, Embase, Web of Science, and the Cochrane Library were thoroughly retrieved until April 22, 2025 to collect studies on the link of NLR to prognosis among the EC population following neoadjuvant therapy. Eligible studies were selected as per predefined eligibility criteria. The primary outcomes encompassed overall survival (OS), recurrence-free survival (RFS), and pathological complete response (pCR). Hazard ratios (HRs) and corresponding 95% confidence intervals (CIs) were pooled for prognostic significance assessment along with subgroup analyses. The evidence was graded via the GRADE method.

Results: 11 cohort studies involving 2,220 patients were included in the analysis. The results demonstrated a notable link of risen NLR to less favorable OS (HR = 1.99, 95% CI: 1.43-2.76, P < 0.0001; I² = 88%), shorter RFS (HR = 2.69, 95% CI: 1.77-4.08, P < 0.00001; I² = 47%), and lower pCR rates (OR = 0.67, 95% CI: 0.47-0.94, P = 0.02; I² = 62%). Subgroup analyses by sample size, follow-up length, age, treatment modality, and NLR cut-off value consistently demonstrated a strong correlation between elevated NLR and shortened RFS across all subgroups. Notably, in patients receiving neoadjuvant chemoradiotherapy (NCRT), the link of increased NLR to OS and RFS appeared more robust compared to those receiving neoadjuvant chemotherapy (NCT) alone.

Conclusion: In patients with EC undergoing neoadjuvant therapy, a higher pre-treatment NLR is significantly linked to worse OS and RFS, as well as a lower likelihood of achieving pCR. Therefore, NLR can be a valuable prognostic biomarker in this patient population, potentially aiding clinicians in risk stratification and treatment decision-making.

Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42024610088.

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中性粒细胞与淋巴细胞比值在食管癌患者接受新辅助治疗中的预后价值:一项系统回顾和荟萃分析。
背景:越来越多的研究揭示了中性粒细胞与淋巴细胞比率(NLR)与食管癌(EC)患者接受新辅助治疗的临床结果的关系。然而,目前的研究结果仍然没有定论,而且有些争议。方法:全面检索PubMed、Embase、Web of Science和Cochrane Library,截止2025年4月22日,收集新辅助治疗后EC人群NLR与预后关系的研究。根据预先确定的资格标准选择符合条件的研究。主要结果包括总生存期(OS)、无复发生存期(RFS)和病理完全缓解期(pCR)。合并风险比(hr)和相应的95%置信区间(ci)进行预后显著性评估,并进行亚组分析。通过GRADE方法对证据进行评分。结果:11项队列研究涉及2220例患者纳入分析。结果显示NLR升高与不良OS (HR = 1.99, 95% CI: 1.43-2.76, P < 0.0001; I²= 88%)、RFS缩短(HR = 2.69, 95% CI: 1.77-4.08, P < 0.00001; I²= 47%)和pCR率降低(OR = 0.67, 95% CI: 0.47-0.94, P = 0.02; I²= 62%)有显著联系。根据样本量、随访时间、年龄、治疗方式和NLR临界值进行的亚组分析一致表明,在所有亚组中NLR升高与RFS缩短之间存在很强的相关性。值得注意的是,在接受新辅助放化疗(NCRT)的患者中,与单独接受新辅助化疗(NCT)的患者相比,NLR增加与OS和RFS的联系更为明显。结论:在接受新辅助治疗的EC患者中,较高的治疗前NLR与较差的OS和RFS以及较低的实现pCR的可能性显著相关。因此,NLR可能是该患者群体中有价值的预后生物标志物,可能有助于临床医生进行风险分层和治疗决策。系统综述注册:https://www.crd.york.ac.uk/prospero/,标识符CRD42024610088。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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