Cancers (Oct 2021)

Liver Decompensation as Late Complication in HCC Patients with Long-Term Response following Selective Internal Radiation Therapy

  • Diederick J. van Doorn,
  • Pim Hendriks,
  • Mark C. Burgmans,
  • Daphne D. D. Rietbergen,
  • Minneke J. Coenraad,
  • Otto M. van Delden,
  • Roel J. Bennink,
  • Tim A. Labeur,
  • Heinz-Josef Klümpen,
  • Ferry A. L. M. Eskens,
  • Adriaan Moelker,
  • Erik Vegt,
  • Dave Sprengers,
  • Nahid Mostafavi,
  • Jan Ijzermans,
  • R. Bart Takkenberg

DOI
https://doi.org/10.3390/cancers13215427
Journal volume & issue
Vol. 13, no. 21
p. 5427

Abstract

Read online

Selective internal radiation therapy (SIRT) is used as a treatment for hepatocellular carcinoma (HCC). The aim of this study was to assess long-term liver-related complications of SIRT in patients who had not developed radioembolization-induced liver disease (REILD). The primary outcome was the percentage of patients without REILD that developed Child-Pugh (CP) ≥ B7 liver decompensation after SIRT. The secondary outcomes were overall survival (OS) and tumor response. These data were compared with a matched cohort of patients treated with sorafenib. Eighty-five patients were included, of whom 16 developed REILD. Of the remaining 69 patients, 38 developed liver decompensation CP ≥ B7. The median OS was 18 months. In patients without REILD, the median OS in patients with CP ≥ B7 was significantly shorter compared to those without CP ≥ B7; 16 vs. 31 months. In the case-matched analysis, the median OS was significantly longer in SIRT-treated patients; 16 vs. 8 months in sorafenib. Liver decompensation CP ≥ B7 occurred significantly more in SIRT when compared to sorafenib; 62% vs. 27%. The ALBI score was an independent predictor of liver decompensation (OR 0.07) and OS (HR 2.83). After SIRT, liver decompensation CP ≥ B7 often developed as a late complication in HCC patients and was associated with a shorter OS. The ALBI score was predictive of CP ≥ B7 liver decompensation and the OS, and this may be a valuable marker for patient selection for SIRT.

Keywords