Evidence map›Paper›PMID 42643191›Full record

ArticleFrontiers in oral health2026

Clinical and laboratory biomarker correlates of lip, oral cavity, and pharyngeal cancer status in a large retrospective clinical database.

Amr Sayed Ghanem, Róbert Bata, Renáta Jávorné Erdei, Marianna Móré, Attila Csaba Nagy

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Article in Frontiers in oral health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Amr Sayed GhanemDepartment of Epidemiology, Institute of Health Sciences, Faculty of Health Sciences, University of Debrecen, Debrecen, Hungary.
Róbert BataDepartment of Epidemiology, Institute of Health Sciences, Faculty of Health Sciences, University of Debrecen, Debrecen, Hungary.
Renáta Jávorné ErdeiDepartment of Health Methodology and Prevention, Institute of Health Sciences, Faculty of Health Sciences, University of Debrecen, Nyíregyháza, Hungary.
Marianna MóréInstitute of Social and Sociological Sciences, Faculty of Health Sciences, University of Debrecen, Nyíregyháza, Hungary.
Attila Csaba NagyDepartment of Epidemiology, Institute of Health Sciences, Faculty of Health Sciences, University of Debrecen, Debrecen, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Lip, oral cavity and pharyngeal cancer (LOCP) comprises a clinically relevant spectrum of contiguous head-and-neck malignancies, yet large real-world datasets with linked blood data remain uncommon. This study investigated demographic, comorbidity-related, gingival/periodontal, and routine laboratory correlates of recorded ICD-10 C00-C14 LOCP cancer status. Methods: This patient-level cross-sectional study included 333,807 unique patients from 805,989 clinical records at the University of Debrecen between 2007 and 2022. Descriptive analyses used Pearson's chi-squared and Wilcoxon rank-sum tests. Multivariable logistic regression was applied in four primary models. Results: Overall, 1,963 patients (0.59%) had recorded LOCP cancer status. In the base clinical model, LOCP cancer status was associated with male sex (OR=3.95, 95% CI: 3.56-4.38), age 45-64 years (OR=10.67, 95% CI: 8.86-12.86), age ≥65 years (OR=7.27, 95% CI: 5.97-8.85), and K05-coded gingival/periodontal disease (OR=8.23, 95% CI: 6.16-10.98). Among biomarkers, log-transformed CRP showed the clearest independent association (OR per 1-SD increase = 1.55, 95% CI: 1.47-1.65), while hemoglobin was inversely associated (OR per 1-SD increase = 0.74, 95% CI: 0.71-0.79). CRP quartiles showed a graded pattern, with Q4 associated with higher odds than Q1 (OR=3.73, 95% CI: 3.01-4.63). Biomarkers modestly improved AUC in complete-case subsets. Conclusions: Recorded LOCP cancer status was associated with a distinct inflammatory and hematological profile, mainly higher CRP and lower hemoglobin. Longitudinal, site-specific datasets with richer behavioral and tumor-level information are needed before these markers can be interpreted as predictive or etiological indicators.

Indexed as

C-reactive proteingingival and periodontal diseasehead and neck cancerhemoglobininflammatory biomarkersoral cavity cancerreal-world clinical databaseroutine laboratory biomarkers

Identifiers

PMID42643191
PMCPMC13503193

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.