The Impact of Sorafenib in Combination with Transarterial Chemoembolization on the Outcomes of Intermediate-Stage Hepatocellular Carcinoma.
Aged
Aged, 80 and over
Antineoplastic Agents
/ therapeutic use
Carcinoma, Hepatocellular
/ mortality
Chemoembolization, Therapeutic
Combined Modality Therapy
Female
Humans
Liver Neoplasms
/ mortality
Male
Middle Aged
Neoplasm Staging
Retrospective Studies
Sorafenib
/ therapeutic use
Survival Rate
Treatment Outcome
Intermediate-stage hepatocellular carcinoma
Transarterial chemoembolization-refractory
sorafenib
Journal
Asian Pacific journal of cancer prevention : APJCP
ISSN: 2476-762X
Titre abrégé: Asian Pac J Cancer Prev
Pays: Thailand
ID NLM: 101130625
Informations de publication
Date de publication:
01 Apr 2021
01 Apr 2021
Historique:
received:
04
01
2021
entrez:
28
4
2021
pubmed:
29
4
2021
medline:
24
11
2021
Statut:
epublish
Résumé
We investigated the treatment outcomes and hepatic reserve of transarterial chemoembolization (TACE)-refractory patients with recurrent advanced hepatocellular carcinoma (HCC) treated with TACE plus sorafenib. Forty-one patients with intermediate-stage HCC defined as being TACE refractory on imaging were treated with sorafenib and TACE between 2009 and 2012 and comprised the combination treatment group. Twenty-nine patients who received repeated TACE after becoming refractory to TACE between 2005 and 2008 comprised the TACE continuation group. Although the interval between successive rounds of TACE was significantly shorter before the patients developed TACE refractoriness, it was significantly longer after the development of TACE refractoriness, in the combination treatment group compared with the TACE continuation group. The appearance of extrahepatic spread and/or vascular invasion differed significantly between the two groups. The median overall survival was significantly longer in the combination treatment group than in the TACE continuation group (20.5 vs. 15.4 months, respectively; hazard ratio = 2.04; 95% confidence interval = 1.20-3.48). The 3-year overall survival rate was 33.4% in the combination treatment group and 3.5% in the TACE continuation group. Downstaging of the Child-Pugh class was significantly less frequent in the combination treatment group than in the TACE continuation group. In COX proportional hazards analyses, sorafenib plus TACE resulted in a better prognosis compared with repeated TACE. Treatment with sorafenib plus TACE in TACE-refractory patients with intermediate-stage HCC resulted in longer intervals between TACE rounds, better maintenance of hepatic reserve, and significantly longer OS compared with repeated TACE.
Sections du résumé
BACKGROUND
BACKGROUND
We investigated the treatment outcomes and hepatic reserve of transarterial chemoembolization (TACE)-refractory patients with recurrent advanced hepatocellular carcinoma (HCC) treated with TACE plus sorafenib.
METHODS
METHODS
Forty-one patients with intermediate-stage HCC defined as being TACE refractory on imaging were treated with sorafenib and TACE between 2009 and 2012 and comprised the combination treatment group. Twenty-nine patients who received repeated TACE after becoming refractory to TACE between 2005 and 2008 comprised the TACE continuation group.
RESULTS
RESULTS
Although the interval between successive rounds of TACE was significantly shorter before the patients developed TACE refractoriness, it was significantly longer after the development of TACE refractoriness, in the combination treatment group compared with the TACE continuation group. The appearance of extrahepatic spread and/or vascular invasion differed significantly between the two groups. The median overall survival was significantly longer in the combination treatment group than in the TACE continuation group (20.5 vs. 15.4 months, respectively; hazard ratio = 2.04; 95% confidence interval = 1.20-3.48). The 3-year overall survival rate was 33.4% in the combination treatment group and 3.5% in the TACE continuation group. Downstaging of the Child-Pugh class was significantly less frequent in the combination treatment group than in the TACE continuation group. In COX proportional hazards analyses, sorafenib plus TACE resulted in a better prognosis compared with repeated TACE.
CONCLUSIONS
CONCLUSIONS
Treatment with sorafenib plus TACE in TACE-refractory patients with intermediate-stage HCC resulted in longer intervals between TACE rounds, better maintenance of hepatic reserve, and significantly longer OS compared with repeated TACE.
Identifiants
pubmed: 33906315
doi: 10.31557/APJCP.2021.22.4.1217
pmc: PMC8325117
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Sorafenib
9ZOQ3TZI87
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1217-1224Références
Mol Cancer Ther. 2008 Oct;7(10):3129-40
pubmed: 18852116
Gut. 2020 Aug;69(8):1492-1501
pubmed: 31801872
Eur J Cancer. 2011 Sep;47(14):2117-27
pubmed: 21664811
Hepatology. 2003 Feb;37(2):429-42
pubmed: 12540794
Liver Cancer. 2014 May;3(2):119-24
pubmed: 24945002
Semin Liver Dis. 1999;19(3):271-85
pubmed: 10518307
Hepatology. 2018 Jan;67(1):358-380
pubmed: 28130846
Nat Rev Cancer. 2013 Feb;13(2):123-35
pubmed: 23344543
Hepatology. 2011 Mar;53(3):1020-2
pubmed: 21374666
Gastroenterology. 2004 Nov;127(5 Suppl 1):S5-S16
pubmed: 15508102
Am J Gastroenterol. 2008 Apr;103(4):914-21
pubmed: 18177453
Oncology. 2014;87(6):330-41
pubmed: 25227534
N Engl J Med. 2008 Jul 24;359(4):378-90
pubmed: 18650514
Dig Dis. 2017;35(6):602-610
pubmed: 29040999
Lancet Oncol. 2009 Jan;10(1):25-34
pubmed: 19095497
Lancet. 2018 Mar 31;391(10127):1301-1314
pubmed: 29307467
Liver Cancer. 2016 Nov;6(1):16-26
pubmed: 27995084
Oncology. 2014;87 Suppl 1:22-31
pubmed: 25427730
J Hepatol. 2016 May;64(5):1090-1098
pubmed: 26809111
Lancet Gastroenterol Hepatol. 2017 Aug;2(8):565-575
pubmed: 28648803
Hepatol Int. 2017 Jul;11(4):317-370
pubmed: 28620797
Clin Drug Investig. 2015 Nov;35(11):751-9
pubmed: 26446004
N Engl J Med. 2020 May 14;382(20):1894-1905
pubmed: 32402160
J Hepatol. 2018 Jul;69(1):182-236
pubmed: 29628281
Liver Cancer. 2015 Dec;4(4):253-62
pubmed: 26734579
Cancer Sci. 2008 Oct;99(10):2037-44
pubmed: 19016764
J Vasc Interv Radiol. 2018 Aug;29(8):1061-1067
pubmed: 29934260