View : 760 Download: 0

Full metadata record

DC Field Value Language
dc.contributor.author김휘영*
dc.date.accessioned2019-04-16T16:30:14Z-
dc.date.available2019-04-16T16:30:14Z-
dc.date.issued2019*
dc.identifier.issn0168-8278*
dc.identifier.issn1600-0641*
dc.identifier.otherOAK-24577*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/249644-
dc.description.abstractBackground & Aims: Sorafenib is first-line standard of care for patients with advanced hepatocellular carcinoma (HCC), yet it confers limited survival benefit. Therefore, we aimed to compare clinical outcomes of sorafenib combined with concurrent conventional transarterial chemoembolization (cTACE) vs. sorafenib alone in patients with advanced HCC. Methods: In this investigator-initiated, multicenter, phase III trial, patients were randomized to receive sorafenib alone (Arm S, n = 169) or in combination with cTACE on demand (Arm C, n = 170). Sorafenib was started within 3 days and cTACE within 7-21 days of randomization. The primary endpoint was overall survival (OS). Results: For Arms C and S, the median OS was 12.8 vs. 10.8 months (hazard ratio [HR] 0.91; 90% CI 0.69-1.21; p = 0.290); median time to progression, 5.3 vs. 3.5 months (HR 0.67; 90% CI 0.53-0.85; p = 0.003); median progression-free survival, 5.2 vs. 3.6 months (HR 0.73; 90% CI 0.59-0.91; p = 0.01); and tumor response rate, 60.6% vs. 47.3% (p = 0.005). For Arms C and S, serious (grade = 3) adverse events occurred in 33.3% vs. 19.8% (p = 0.006) of patients and included increased alanine aminotransferase levels (20.3% vs. 3.6%), hyperbilirubinemia (11.8% vs. 3.0%), ascites (11.8% vs. 4.2%), thrombocytopenia (7.2% vs. 1.2%), anorexia (7.2% vs. 1.2%), and hand-foot skin reaction (10.5% vs. 11.4%). A post hoc subgroup analysis compared OS in Arm C patients (46.4%) receiving >= 2 cTACE sessions to Arm S patients (18.6 vs. 10.8 months; HR 0.58; 95% CI 0.40-0.82; p = 0.006). Conclusion: Compared with sorafenib alone, sorafenib combined with cTACE did not improve OS in patients with advanced HCC. However, sorafenib combined with cTACE significantly improved time to progression, progression-free survival, and tumor response rate. Sorafenib alone remains the first-line standard of care for patients with advanced HCC. Lay summary: For patients with advanced hepatocellular carcinoma requiring sorafenib therapy, co-administration with conventional transarterial chemoembolization did not improve overall survival compared to sorafenib alone. Therefore, sorafenib alone remains the first-line standard of care for patients with advanced hepatocellular carcinoma. (C) 2018 European Association for the Study of the Liver. Published by Elsevier B.V.*
dc.languageEnglish*
dc.publisherELSEVIER SCIENCE BV*
dc.subjectHepatocellular carcinoma*
dc.subjectSorafenib*
dc.subjectTransarterial chemoembolization*
dc.subjectCombination treatment*
dc.titleSorafenib with or without concurrent transarterial chemoembolization in patients with advanced hepatocellular carcinoma: The phase III STAH trial*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume70*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage684*
dc.relation.lastpage691*
dc.relation.journaltitleJOURNAL OF HEPATOLOGY*
dc.identifier.doi10.1016/j.jhep.2018.11.029*
dc.identifier.wosidWOS:000461333700013*
dc.author.googlePark, Joong-Won*
dc.author.googleKim, Yoon Jun*
dc.author.googleKim, Do Young*
dc.author.googleBae, Si-Hyun*
dc.author.googlePaik, Seung Woon*
dc.author.googleLee, Youn-Jae*
dc.author.googleKim, Hwi Young*
dc.author.googleLee, Han Chu*
dc.author.googleHan, Sang Young*
dc.author.googleCheong, Jae Youn*
dc.author.googleKwon, Oh Sang*
dc.author.googleYeon, Jong Eun*
dc.author.googleKim, Bo Hyun*
dc.author.googleHwang, Jaeseok*
dc.contributor.scopusid김휘영(56493773500)*
dc.date.modifydate20240601081000*
Appears in Collections:
의과대학 > 의학과 > Journal papers
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

BROWSE