Predictive factors of transarterial chemoembolisation toxicity in unresectable hepatocellular carcinoma

Dig Liver Dis. 2014 Apr;46(4):358-62. doi: 10.1016/j.dld.2013.12.012. Epub 2014 Jan 23.

Abstract

Background: Transarterial chemoembolisation (TACE) is an effective treatment for unresectable hepatocellular carcinoma (HCC), but can cause severe toxicity.

Aim: To identify predictive factors of severe TACE-related toxicity in patients with unresectable HCC.

Methods: All HCC patients who underwent TACE at the Dijon University Hospital between 2008 and 2011 were included in this retrospective study. Severe TACE-related toxicity was defined as the occurrence of any adverse event grade ≥ 4, or any adverse event that caused a prolongation of hospitalisation of >8 days, or any additional hospitalisation within 1 month after TACE. Factors predicting toxicity were identified using a logistic regression model. The robustness of the final model was confirmed using bootstrapping (500 replications).

Results: 124 patients were included, median age was 67 years and 90% were male; 22 patients (18%) experienced severe TACE-related toxicity. Factors that independently predicted severe TACE-related toxicity in multivariate analysis were total tumour size (OR, 1.15 cm(-1); 95%CI, 1.04-1.26; p=0.01), and high serum AST levels (OR, 1.10 per 10 IU/l; 95%CI, 1.01-1.21; p=0.04). The results were confirmed by bootstrapping.

Conclusions: Total tumour size and high serum AST levels were predictive factors of severe TACE-related toxicity in this hospital-based series of patients with unresectable HCC.

Keywords: Hepatocellular carcinoma; Toxicity; Transarterial chemoembolisation.

MeSH terms

  • Acute Kidney Injury / etiology*
  • Adult
  • Aged
  • Aged, 80 and over
  • Aspartate Aminotransferases / blood
  • Carcinoma, Hepatocellular / complications
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / therapy*
  • Chemical and Drug Induced Liver Injury
  • Chemoembolization, Therapeutic / adverse effects*
  • Chemoembolization, Therapeutic / mortality
  • Cohort Studies
  • Doxorubicin / adverse effects
  • Female
  • Hepatic Encephalopathy / etiology*
  • Hepatitis B, Chronic / complications
  • Hepatitis C, Chronic / complications
  • Humans
  • Idarubicin / adverse effects
  • Liver Cirrhosis / complications
  • Liver Cirrhosis, Alcoholic / complications
  • Liver Failure, Acute / etiology*
  • Liver Neoplasms / complications
  • Liver Neoplasms / pathology
  • Liver Neoplasms / therapy*
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Retrospective Studies
  • Risk Factors
  • Treatment Outcome
  • Tumor Burden

Substances

  • Doxorubicin
  • Aspartate Aminotransferases
  • Idarubicin