Neutrophil-to-lymphocyte ratio as a predictor of outcomes for patients with hepatocellular carcinoma: A Western perspective

Kevin M. Sullivan, Ryan T. Groeschl, Kiran K. Turaga, Susan Tsai, Kathleen K. Christians, Sarah B. White, William S. Rilling, Charles H.C. Pilgrim, T. Clark Gamblin

Research output: Contribution to journalReview articlepeer-review

Abstract

Background and Objectives Neutrophil-to-lymphocyte ratio (NLR) is simple, inexpensive, and has been proposed to be predictive in hepatocellular carcinoma (HCC) in Europe and Asia. We aimed to evaluate whether NLR at presentation in a Western center provides any prognostic value compared to other common prognostic scores. Methods NLR was calculated for 75 consecutive patients at presentation with HCC and regression models were used to analyze its value for predicting treatment strategy and short-term survival with Child-Pugh and Model for End Stage Liver Disease (MELD). Results NLR was not predictive of future treatment regimens with hepatectomy, liver transplant, or transarterial chemoembolization (TACE; odds ratio [OR]: 0.85, 95% confidence interval [CI]: 0.71-1.02, P = 0.079) as compared the predictive value of MELD (OR: 0.81, CI: 0.72-0.93, P = 0.002) or Child-Pugh (OR: 0.48, CI: 0.34-0.69, P < 0.001). Adding additional adjustment for treatment, NLR did not correlate with short-term overall survival (hazard ratio [HR]: 1.09, CI: 0.95-1.24, P = 0.227). MELD also did not correlate with overall survival (HR: 1.04, CI: 0.96-1.13, P = 0.357) whereas Child-Pugh (HR: 1.56, CI: 1.10-2.19, P = 0.011) was predictive. Conclusions This study does not support the prognostic value of NLR to guide therapy for HCC in a Western center, whereas MELD and Child-Pugh score were more predictive. J. Surg. Oncol. 2014 109:95-97.

Original languageEnglish (US)
Pages (from-to)95-97
Number of pages3
JournalJournal of Surgical Oncology
Volume109
Issue number2
DOIs
StatePublished - Feb 2014

Keywords

  • hepatocellular carcinoma
  • inflammation
  • neutrophil-to-lymphocyte ratio

ASJC Scopus subject areas

  • Surgery
  • Oncology

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