A differential risk assessment and decision model for Transarterial chemoembolization in hepatocellular carcinoma based on hepatic function

BMC Cancer. 2020 Jun 1;20(1):504. doi: 10.1186/s12885-020-06975-2.

Abstract

Background: The decision of transarterial chemoembolization (TACE) initiation and/or repetition remains challenging in patients with unresectable hepatocellular carcinoma (HCC). The aim was to develop a prognostic scoring system to guide TACE initiation/repetition.

Methods: A total of 597 consecutive patients who underwent TACE as their initial treatment for unresectable HCC were included. We derived a prediction model using independent risk factors for overall survival (OS), which was externally validated in an independent cohort (n = 739).

Results: Independent risk factors of OS included Albumin-bilirubin (ALBI) grade, maximal tumor size, alpha-fetoprotein, and tumor response to initial TACE, which were used to develop a scoring system ("ASAR"). C-index values for OS were 0.733 (95% confidence interval [CI] = 0.570-0.871) in the derivation, 0.700 (95% CI = 0.445-0.905) in the internal validation, and 0.680 (95% CI = 0.652-0.707) in the external validation, respectively. Patients with ASAR< 4 showed significantly longer OS than patients with ASAR≥4 in all three datasets (all P < 0.001). Among Child-Pugh class B patients, a modified model without TACE response, i.e., "ASA(R)", discriminated OS with a c-index of 0.788 (95% CI, 0.703-0.876) in the derivation, and 0.745 (95% CI, 0.646-0.862) in the internal validation, and 0.670 (95% CI, 0.605-0.725) in the external validation, respectively. Child-Pugh B patients with ASA(R) < 4 showed significantly longer OS than patients with ASA(R) ≥ 4 in all three datasets (all P < 0.001).

Conclusions: ASAR provides refined prognostication for repetition of TACE in patients with unresectable HCC. For Child-Pugh class B patients, a modified model with baseline factors might guide TACE initiation.

Keywords: Child-Pugh classification; Hepatocellular carcinoma; Risk prediction model; Transarterial chemoembolization.

Publication types

  • Validation Study

MeSH terms

  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Bilirubin / analysis
  • Carcinoma, Hepatocellular / blood
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / physiopathology
  • Carcinoma, Hepatocellular / therapy*
  • Chemoembolization, Therapeutic / methods*
  • Clinical Decision-Making / methods
  • Doxorubicin / administration & dosage
  • Female
  • Follow-Up Studies
  • Humans
  • Liver / pathology
  • Liver / physiopathology
  • Liver Cirrhosis / blood
  • Liver Cirrhosis / diagnosis*
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / physiopathology
  • Liver Function Tests
  • Liver Neoplasms / blood
  • Liver Neoplasms / pathology
  • Liver Neoplasms / physiopathology
  • Liver Neoplasms / therapy*
  • Male
  • Middle Aged
  • Models, Biological
  • Response Evaluation Criteria in Solid Tumors
  • Risk Assessment / methods
  • Risk Factors
  • Serum Albumin / analysis
  • Severity of Illness Index
  • Survival Analysis

Substances

  • Antineoplastic Agents
  • Serum Albumin
  • Doxorubicin
  • Bilirubin