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Prognostic value of NLR and PLR in oral squamous cell carcinoma patients: A cohort study from tertiary cancer center.

Created on 30 Oct 2026

Authors

Vandana Mohta, Renuka Badanale, Shilpa Nellikkal

Published in

Journal of cancer research and therapeutics. Volume 22. Issue 5. Pages 826-831. Jul 01, 2026. Epub Oct 29, 2026.

Abstract

Oral cancer remains a major health burden in developing countries like India and across South-East Asia. There is a need for newer, cheaper, and reliable biomarkers to aid in early detection, prognosis, and personalized treatment strategies.
A cohort study of 110 operated oral squamous cell carcinoma (OSCC) patients was conducted at a tertiary cancer center in India (January 2020-May 2021). Neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and clinicopathological features were analyzed using Statistical Package for the Social Sciences version 28.0. Associations with tumor characteristics were assessed via Mann-Whitney U and Chi-square tests. R curves and Youden's index identified optimal NLR/PLR cutoffs. Overall survival (OS) and disease-free survival (DFS) were analyzed using Kaplan-Meier and compared with the log-rank test ( P < 0.05 considered significant).
Among 110 patients (87 men, 23 women; age 22-72), buccal mucosa was the most common tumor site (42.7%), with most in stage IV. Mean follow-up was 15.5 months. NLR showed good prognostic value (AUC (area under the curve): 0.733; cutoff: 3.04), and PLR showed fair value (AUC: 0.640; cutoff: 131.28). Both were significantly higher in females ( P = 0.005, 0.021). Higher NLR was linked to recurrence ( P = 0.03), and PLR was associated with higher TNM stage ( P = 0.040) and bone involvement ( P = 0.034). Low NLR and PLR correlated with better DFS ( P = 0.000, 0.012); low NLR also showed a trend toward better OS ( P = 0.059).
NLR and PLR are cost-effective, accessible prognostic biomarkers in OSCC and are significantly associated with recurrence, advanced disease, and survival outcomes.

PMID:
42955962
Bibliographic data and abstract were imported from PubMed on 30 Oct 2026.

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