Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 43 min ago
Peer-reviewedCC BY-NC-NDTranslational andrology and urology

Prognostic value of neutrophil-to-lymphocyte ratio in renal cell carcinoma: an updated systematic review and meta-analysis.

  1. 1Department of Urology, People's Hospital of Wenshan Zhuang and Miao Autonomous Prefecture, Wenshan, China.

Abstract

The neutrophil-to-lymphocyte ratio (NLR) has been proposed as a prognostic biomarker in renal cell carcinoma (RCC), and meta-analyses have confirmed an association between elevated NLR and poorer survival. However, these meta-analyses are limited by small sample sizes, search dates, insufficient evaluation of cancer-specific survival (CSS), and lack of subgroup analyses examining whether NLR's prognostic value differs by treatment, stage, region, or cut-off. Therefore, this updated systematic review and meta-analysis aimed to comprehensively evaluate the prognostic value of NLR in patients with RCC and to examine whether this association varies across treatment modalities, disease stages, geographic regions, and NLR cut-off values. This updated meta-analysis was registered with PROSPERO (CRD42025637957) and followed PRISMA 2020. We searched PubMed, Embase, Web of Science, and Cochrane Library to August 2026. Eligible cohort studies enrolled confirmed RCC patients of subtype/stage, classified by NLR cut-off, and reported hazard ratios (HRs) with 95% confidence intervals (CIs) for overall survival (OS), CSS, recurrence-free survival (RFS), or disease-free survival (DFS). Quality and certainty were assessed using the Newcastle-Ottawa Scale (NOS) and Grading of Recommendations Assessment, Development and Evaluation (GRADE), respectively. Pooled HRs were calculated using a random-effects model; heterogeneity was quantified by Q and I2. Subgroup analyses and meta-regression explored heterogeneity; funnel plots and Egger's test assessed publication bias. Twenty-six studies (6,041 patients) were included. Elevated NLR was associated with shorter OS (HR =1.93; 95% CI: 1.56-2.39; I2=71%), RFS (HR =2.64; 95% CI: 1.79-3.91; I2=35%), and DFS (HR =1.64; 95% CI: 1.29-2.08; I2=82%), but not CSS (HR =1.62; 95% CI: 0.51-5.13; I2=60%). Subgroup analyses showed NLR predicted OS/DFS in Asian/European but not American, and lost DFS prediction at cut-off ≥3. NLR effect was significant in both surgical and non-surgical subgroups. NOS scores were 7-8; incomplete confounder adjustment common. The certainty of evidence for the OS analysis was rated as very low according to GRADE. Sensitivity analyses confirmed the robustness of the pooled estimates, and Egger's test showed no significant publication bias for OS, RFS, or DFS. This meta-analysis confirms NLR predicts poorer OS, RFS, and DFS in RCC, but adds context-dependent evidence: not significant in Americans, weakened for DFS at higher cut-offs, and not for CSS. These findings refine NLR's utility and support cautious use as a risk-stratification biomarker, noting geography and thresholds. Future prospective studies with standardized cut-offs and confounder adjustment are needed.

Related

  1. Prognostic value of neutrophil-to-lymphocyte ratio in nasopharyngeal carcinoma: a systematic review and meta-analysis of 30 cohorts through June 30, 2026
    Yunliang Lu, Biaoyou Chen, Jingfeng Ye +4
    Translational cancer researchPeer-reviewedCC BY-NC-NDFull textGeneral medicineEurope PMC
  2. Prognostic value of the neutrophil-to-lymphocyte ratio in patients with colorectal cancer undergoing chemotherapy: a systematic review and meta-analysis
    Yihui Zhang, Ning Ding, Yingchao Cui +2
    Frontiers in oncologyPeer-reviewedCC BYFull textOncologyEurope PMC
  3. The Prognostic Value of Baseline Neutrophil-to-Lymphocyte Ratio for Mortality in Idiopathic Pulmonary Fibrosis: A Systematic Review and Meta-Analysis.
    Suprava Shakya, Xingxiang Xu
    CureusPeer-reviewedCC BYFull textOncologyEurope PMC
  4. Predictive and Prognostic Role of Neutrophil-to-Lymphocyte Ratio in Diabetic Nephropathy: Protocol for a Systematic Review and Meta-Analysis
    Aryan K Sharma, Alexandra E Avanu, Juan Felipe Espitia Jaramillo +2
    JMIR Research ProtocolsPeer-reviewedCC BY 4.0Full textEndocrinology & metabolismPMC
  5. Admission blood glucose and neutrophil-to-lymphocyte ratio provide independent and complementary prognostic value for in-hospital mortality in acute type A aortic dissection
    Jianming Bi, Guoqiang Liu, Xiujie Duan +4
    MedicinePeer-reviewedCC BY-NCFull textGeneral medicineEurope PMC
BibTeX
@article{luo2026prognostic,
  title = {{Prognostic value of neutrophil-to-lymphocyte ratio in renal cell carcinoma: an updated systematic review and meta-analysis.}},
  author = {Zhenglei Luo and Zhenxiang Lin and Xiaofang Chen and Zhaoxin Kuang},
  journal = {Translational andrology and urology},
  year = {2026},
  month = sep,
  doi = {10.21037/tau-2026-0558},
  url = {https://europepmc.org/article/MED/42997244},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Prognostic value of neutrophil-to-lymphocyte ratio in renal cell carcinoma: an updated systematic review and meta-analysis.
AU  - Zhenglei Luo
AU  - Zhenxiang Lin
AU  - Xiaofang Chen
AU  - Zhaoxin Kuang
PY  - 2026
DA  - 2026/09/28
JO  - Translational andrology and urology
DO  - 10.21037/tau-2026-0558
UR  - https://europepmc.org/article/MED/42997244
AB  - The neutrophil-to-lymphocyte ratio (NLR) has been proposed as a prognostic biomarker in renal cell carcinoma (RCC), and meta-analyses have confirmed an association between elevated NLR and poorer survival. However, these meta-analyses are limited by small sample sizes, search dates, insufficient evaluation of cancer-specific survival (CSS), and lack of subgroup analyses examining whether NLR's prognostic value differs by treatment, stage, region, or cut-off. Therefore, this updated systematic review and meta-analysis aimed to comprehensively evaluate the prognostic value of NLR in patients with RCC and to examine whether this association varies across treatment modalities, disease stages, geographic regions, and NLR cut-off values. This updated meta-analysis was registered with PROSPERO (CRD42025637957) and followed PRISMA 2020. We searched PubMed, Embase, Web of Science, and Cochrane Library to August 2026. Eligible cohort studies enrolled confirmed RCC patients of subtype/stage, classified by NLR cut-off, and reported hazard ratios (HRs) with 95% confidence intervals (CIs) for overall survival (OS), CSS, recurrence-free survival (RFS), or disease-free survival (DFS). Quality and certainty were assessed using the Newcastle-Ottawa Scale (NOS) and Grading of Recommendations Assessment, Development and Evaluation (GRADE), respectively. Pooled HRs were calculated using a random-effects model; heterogeneity was quantified by Q and I2. Subgroup analyses and meta-regression explored heterogeneity; funnel plots and Egger's test assessed publication bias. Twenty-six studies (6,041 patients) were included. Elevated NLR was associated with shorter OS (HR =1.93; 95% CI: 1.56-2.39; I2=71%), RFS (HR =2.64; 95% CI: 1.79-3.91; I2=35%), and DFS (HR =1.64; 95% CI: 1.29-2.08; I2=82%), but not CSS (HR =1.62; 95% CI: 0.51-5.13; I2=60%). Subgroup analyses showed NLR predicted OS/DFS in Asian/European but not American, and lost DFS prediction at cut-off ≥3. NLR effect was significant in both surgical and non-surgical subgroups. NOS scores were 7-8; incomplete confounder adjustment common. The certainty of evidence for the OS analysis was rated as very low according to GRADE. Sensitivity analyses confirmed the robustness of the pooled estimates, and Egger's test showed no significant publication bias for OS, RFS, or DFS. This meta-analysis confirms NLR predicts poorer OS, RFS, and DFS in RCC, but adds context-dependent evidence: not significant in Americans, weakened for DFS at higher cut-offs, and not for CSS. These findings refine NLR's utility and support cautious use as a risk-stratification biomarker, noting geography and thresholds. Future prospective studies with standardized cut-offs and confounder adjustment are needed.
SN  - 2223-4691
ER  -