Serum YKL-40 independently predicts outcome after transcatheter arterial chemoembolization of hepatocellular carcinoma

PLoS One. 2012;7(9):e44648. doi: 10.1371/journal.pone.0044648. Epub 2012 Sep 6.

Abstract

Background: Transcatheter arterial chemoembolization (TACE) is the most widely used treatment option for unresectable hepatocellular carcinoma (HCC). Elevated serum YKL-40 level has been shown to predict poor prognosis in HCC patients undergoing resection. This study was designed to validate the prognostic significance of serum YKL-40 in patients with HCC undergoing TACE treatment.

Methods: Serum YKL-40 level was determined by enzyme-linked immunosorbent assay. Overall survival (OS) was evaluated with the Kaplan-Meier method and compared by the log-rank test. Multivariate study with Cox proportional hazard model was used to evaluate independent prognostic variables of OS.

Results: The median pretreatment serum YKL-40 in HCC patients with was significantly higher than that in healthy controls (P<0.001). The YKL-40 could predict survival precisely either in a dichotomized or continuous fashion (P<0.001 and P = 0.001, respectively). Multivariate Cox regression analysis indicated that serum YKL-40 was an independent prognostic factor for OS in HCC patients (P = 0.001). In further stratified analyses, YKL-40 could discriminate the outcomes of patients with low and high alpha-fetoprotein (AFP) level (P = 0.006 and 0.016, respectively). Furthermore, the combination of serum YKL-40 and AFP had more capacity to predict patients' outcomes.

Conclusions: Serum YKL-40 was demonstrated to be an independent prognostic biomarker in HCC patients treated with TACE. Our results need confirmation in an independent study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipokines / blood*
  • Adolescent
  • Adult
  • Aged
  • Carcinoma, Hepatocellular / drug therapy*
  • Catheterization, Central Venous*
  • Chemoembolization, Therapeutic*
  • Chitinase-3-Like Protein 1
  • Female
  • Humans
  • Lectins / blood*
  • Liver Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Young Adult

Substances

  • Adipokines
  • CHI3L1 protein, human
  • Chitinase-3-Like Protein 1
  • Lectins

Grants and funding

This study was supported by a research fund of the authors’ hospital (Jinan Infectious Disease Hospital, Shandong University). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.