language Türkçe
Article 2024 · 3 citations

A novel prognostic biomarker in progression free survival for patients with cervical cancer, glucose to c-reactive protein ratio (GCR)

Buyukbayram, Mehmet Emin, Hannarici, Zekeriya, Turhan, Aykut, Caglar, Alperen Akansel, Esdur, Pinar coban, Bilici, Mehmet, Tekin, Salim Basol, Erdemci, Burak

Abstract

Background Cervical cancer is a tumor with high morbidity and mortality. The importance of inflammatory and metabolic parameters affecting progression-free survival (PFS) and overall survival (OS) has been investigated more intensively recently. We aimed to investigate the effect of glucose/c-reactive protein (CRP) ratio [GCR], which shows these two parameters together, on PFS in cervical cancer. Methods We retrospectively included 90 patients with adenocarcinoma and squamous cell carcinoma of the cervix. The effects of clinical variables, inflammatory and glycemic parameters on PFS and OS were analyzed by Kaplan-Meier method. The data were compared with the healthy control group of 90 individuals using the independent t test. The effect of parameters on mortality was analyzed using ROC curves and cut off values were determined. Results Glucose, CRP, CRP/lymphocyte ratio (CLR) and GCR were statistically significant in predicting mortality (p < 0.05). Disease stage, glucose, CRP, CLR and GCR were associated with overall survival. CRP, CLR and GCR were associated with progression-free survival (p < 0.05). In multivariate analysis, GCR was prognostic for PFS (p = 0.025). GCR was statistically significant while compared with the patient and healthy control group (p < 0.001). Conclusion In cervical cancer, GCR rate was found to be prognostic independent of stage. Higher GCR rate was associated with longer PFS duration.

Keywords
Cervical cancer glucose/c-reactivated protein ratio Progression-free survival UNITED-STATES INFLAMMATION CRP STATISTICS LYMPHOCYTE RECURRENCE TRENDS CEA
WoS Categories
Oncology
Sustainable Development Goals
Citation
Journal
BMC CANCER
Year
2024
Volume
24
Issue
1
eISSN
1471-2407
DOI
10.1186/s12885-024-12347-x
WoS UID
WOS:001230301600009
Open via DOI