Elevated Baseline Neutrophil Count Correlates with Worse Outcomes in Patients with Muscle-Invasive Bladder Cancer Treated with Chemoradiation

Author:

Meunier Sébastien1,Frontczak Alexandre2,Balssa Loïc2,Blanc Julie3,Benhmida Salim4,Pernot Mandy4,Quivrin Magali1,Martin Etienne1,Hammoud Yasser4,Créhange Gilles5,Boustani Jihane46

Affiliation:

1. Department of Radiation Oncology, Centre Georges François Leclerc, 21000 Dijon, France

2. Department of Urology, University Hospital of Besançon, 25000 Besançon, France

3. Department of Biostatistics, Centre Georges François Leclerc, 21000 Dijon, France

4. Department of Radiation Oncology, University Hospital of Besançon, 25000 Besançon, France

5. Department of Radiation Oncology, Institut Curie, 92210 Saint-Cloud, France

6. INSERM, EFS BFC, UMR1098, RIGHT, Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire et Génique, University of Bourgogne Franche-Comté, 25000 Besançon, France

Abstract

Background: The role of inflammation in the development and prognosis of bladder cancer (BC) is now established. We evaluated the significance of neutrophil-to-lymphocyte ratio (NLR) and neutrophil count (PNN) in patients with localized BC treated with chemoradiation. Methods: Clinical characteristics and baseline biological data were retrospectively collected. We tested the association between NLR, PNN, and overall survival (OS) and progression-free survival (PFS). Results: One hundred and ninety-four patients were included. Median PNN was 4000.0/mm3 [1500.0–16,858.0] and median NLR was 2.6 [0.6–19.2]. In patients with NLR > 2.6, median OS and PFS were lower (OS: 25.5 vs. 58.4 months, p = 0.02; PFS: 14.1 vs. 26.7 months, p = 0.07). Patients with PNN > 4000/mm3 had significantly lower OS (21.8 vs. 70.1 months, p < 0.001) and PFS (13.7 vs. 38.8 months, p < 0.001). Contrary to NLR, PNN > 4000/mm3 was associated with shorter OS and PFS in multivariate analysis. Conclusions: Elevated PNN at baseline was associated with worse OS and PFS. NLR was not an independent prognostic factor.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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