# Diagnostic Value of the Delta Neutrophil Index and Neutrophil-to-Lymphocyte Ratio for Preoperative Differentiation of Malignant and Benign Primary Brain Tumors: A Retrospective Cohort Study

**Authors:** Emrullah Cem Kesilmez, Muharrem Furkan Yüzbaşı, Muhammed Kırkgeçit, Hasan Türkoğlu, Kasım Zafer Yüksel

PMC · DOI: 10.3390/brainsci16020169 · Brain Sciences · 2026-01-30

## TL;DR

This study shows that blood tests measuring neutrophil levels can help tell if a brain tumor is cancerous before surgery.

## Contribution

The study introduces the combined use of DNI and NLR as noninvasive tools for preoperative brain tumor malignancy assessment.

## Key findings

- DNI and NLR showed high accuracy in distinguishing malignant from benign brain tumors.
- The combined model of DNI and NLR achieved an AUC of 0.937, with 88.3% sensitivity and 86.0% specificity.
- DNI was identified as the most powerful independent predictor of malignancy.

## Abstract

Aim: This study aimed to evaluate the diagnostic performance of the Delta Neutrophil Index (DNI) and Neutrophil-to-Lymphocyte Ratio (NLR) in distinguishing malignant from benign primary brain tumors during the preoperative period. Methods: This retrospective cohort study was conducted at a tertiary university hospital. A total of 140 participants were included 60 patients with malignant glial tumors, 50 patients with benign brain tumors, and 30 healthy controls without inflammatory, infectious, or hematologic disease. Preoperative complete blood count results obtained within seven days before surgery were analyzed. Results: Patients with malignant tumors were significantly older than those in the benign and control groups (p < 0.001). DNI, NLR, PLR, MLR, and SII values were all significantly elevated in the malignant group (p < 0.001, for all comparisons). ROC analysis revealed high diagnostic accuracy for DNI (AUC = 0.847) and NLR (AUC = 0.850), with optimal cut-off values of 3.50 and 3.95, respectively. In multivariable logistic regression adjusted for age, DNI > 3.5 (OR = 20.67; 95% CI: 3.35–127.64; p = 0.001), NLR > 3.95 (OR = 21.17; 95% CI: 3.28–136.50; p = 0.001), and CRP (OR = 1.52; 95% CI: 1.20–1.93; p = 0.001) remained independent predictors of malignancy. The combined model including DNI and NLR achieved the highest diagnostic accuracy (AUC = 0.937; age-adjusted AUC = 0.943), with a sensitivity of 88.3% and a specificity of 86.0% after age adjustment. Conclusions: Both DNI and NLR demonstrated significant value in differentiating malignant from benign primary brain tumors prior to surgery, with DNI emerging as the most powerful independent predictor. The combined use of DNI and NLR substantially improved diagnostic accuracy, suggesting that simple hematologic indices may serve as practical, noninvasive adjunctive tools in the preoperative assessment of brain tumor malignancy. These markers may assist in surgical prioritization, patient counseling, and clinical decision-making, particularly in resource-limited settings.

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MPO (myeloperoxidase) [NCBI Gene 4353], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** neurological symptom (MESH:D009461), anaplastic astrocytoma (MESH:D001254), renal cell carcinoma (MESH:D002292), intracranial mass (MESH:C536030), glioblastoma (MESH:D005909), inflammatory, infectious, or hematologic disease (MESH:D003141), systemic disease (MESH:D034721), Primary Brain Tumors (MESH:D001932), chronic (MESH:D002908), sepsis (MESH:D018805), breast cancer (MESH:D001943), systemic (MESH:D015619), infection (MESH:D007239), pituitary adenoma (MESH:D010911), benign tumors (MESH:D009369), gastrointestinal disorders (MESH:D005767), central nervous system tumors (MESH:D016543), schwannoma (MESH:D009442), edema (MESH:D004487), Central nervous system malignancies (MESH:D002493), immune-inflammation (MESH:D007249), DNI (MESH:D003699), injury to (MESH:D014947), axillary metastasis (MESH:D009362), NLR (MESH:D015467), glial tumors (MESH:D005910), autoimmune, or hematologic diseases (MESH:D006402), thyroid cancer (MESH:D013964), meningioma (MESH:D008579), brain lesion (MESH:D001927), neutrophilia (MESH:C563010)
- **Chemicals:** ethylenediaminetetraacetic acid (MESH:D004492), DNI (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938201/full.md

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Source: https://tomesphere.com/paper/PMC12938201