Oncotarget

Research Papers:

Neutrophil-to-lymphocyte ratio predicts survival in European patients with hepatocellular carcinoma administered sorafenib

Alberto Lué _, Maria Trinidad Serrano, Francisco Javier Bustamante, Mercedes Iñarrairaegui, Juan Ignacio Arenas, Milagros Testillano, Sara Lorente, Cristina Gil, Manuel de la Torre, Alexandra Gomez and Bruno Sangro

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Oncotarget. 2017; 8:103077-103086. https://doi.org/10.18632/oncotarget.21528

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Abstract

Alberto Lué1,2, Maria Trinidad Serrano1,2, Francisco Javier Bustamante3, Mercedes Iñarrairaegui4,5, Juan Ignacio Arenas6, Milagros Testillano3, Sara Lorente1,2, Cristina Gil3, Manuel de la Torre4, Alexandra Gomez6 and Bruno Sangro4,5

1Department of Gastroenterology, Hospital Clínico Universitario Lozano Blesa, 50009, Zaragoza, Spain

2Instituto de Investigación Sanitaria (IIS) Aragón, 50009, Zaragoza, Spain

3Department of Gastroenterology, Hospital Universitario Cruces, Plaza de Cruces, 48903, Barakaldo, Spain

4Liver Unit, Clinica Universidad de Navarra-IDISNA, 31008, Pamplona, Spain

5Centro de Investigacion Biomedica en Red de Enfermedades Hepaticas y Digestivas (CIBEREHD), 31008, Pamplona, Spain

6Department of Gastroenterology, Hospital Universitario Donostia, Begiristain Doktorea Pasealekua, 20014, San Sebastian, Spain

Correspondence to:

Alberto Lué, email: [email protected]

Keywords: neutrophil-to-lymphocyte ratio, hepatocellular carcinoma, sorafenib, overall survival

Received: February 15, 2017     Accepted: September 21, 2017     Published: October 05, 2017

ABSTRACT

Neutrophil-to-lymphocyte ratio (NLR) is considered a prognostic factor in patients with hepatocellular carcinoma (HCC). Our aim is to investigate the prognostic significance of NLR in patients with HCC treated with sorafenib.

Results: Median follow-up time was 7 months. Patients were mostly in the intermediate (27.3%) or advanced (72.7%) BCLC stages, 38.6% had vascular invasion and 27.5% extrahepatic disease. A large proportion (38.9%) had been previously treated with TACE. Liver function was preserved: 65.8% were classed as Child A. Median overall survival was 7.7 months (95% CI: 5.8–9.6). In univariate analysis, vascular invasion (P = 0.004), ECOG-PS ≥ 1 (P < 0.001), high bilirubin (P < 0.001), clinical ascites (P = 0.036), BCLC stage (P = 0.004), no previous TACE (P = 0.041) and NRL ≥ 2.3 (P = 0.005) were predictors of poor survival. Skin toxicity (P = 0.039) or hypertension (P = 0.033) during treatment were related to better survival. In multivariate analysis NLR ≥ 2.3 [HR 1.72 (95% CI: 1.03–2.71)], hyperbilirubinemia [HR 3.42 (95% CI: 1.87–6.25)] and ECOG-PS ≥ 1 [HR 1.97 (95% CI: 1.19–3.26)] were found as independent indicators of poor overall survival. Dermatologic adverse effects were an indicator of good overall survival [HR 0.59 (95% CI: 0.38–0.92)].

Material and Methods: One hundred and fifty-four consecutive HCC patients treated with sorafenib in four different Spanish hospitals between August 2005 and October 2013 were analysed. Clinical, laboratory, and tumour features were obtained. Survival was calculated from the moment sorafenib treatment was initiated. Log-rank and Cox regression were used to analyse the ability of NLR to predict survival.

Conclusions: NLR is an independent prognostic indicator for overall survival in HCC patients treated with sorafenib.


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