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

Authors :
van Doorn DJ
Hendriks P
Burgmans MC
Rietbergen DDD
Coenraad MJ
van Delden OM
Bennink RJ
Labeur TA
Klümpen HJ
Eskens FALM
Moelker A
Vegt E
Sprengers D
Mostafavi N
Ijzermans J
Takkenberg RB
Source :
Cancers [Cancers (Basel)] 2021 Oct 29; Vol. 13 (21). Date of Electronic Publication: 2021 Oct 29.
Publication Year :
2021

Abstract

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.

Details

Language :
English
ISSN :
2072-6694
Volume :
13
Issue :
21
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
34771591
Full Text :
https://doi.org/10.3390/cancers13215427