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Effectiveness of Transarterial Chemoembolization-First Treatment for Advanced Hepatocellular Carcinoma: A Propensity Score Matching Analysis

Authors
Chung, Sung WonPark, Min KyungCho, Young YounPark, YoungsuLee, Cheol-HyungOh, HyunwooJang, HeejoonKim, Minseok AlbertKim, Sun WoongNam, Joon YeulLee, Yun BinCho, Eun JuYu, Su JongKim, Hyo-CheolKim, Yoon JunChung, Jin WookYoon, Jung-HwanLee, Jeong-Hoon
Issue Date
2021
Publisher
DOVE MEDICAL PRESS LTD
Keywords
liver cancer; transarterial therapy; locoregional therapy; tyrosine kinase inhibitor
Citation
JOURNAL OF HEPATOCELLULAR CARCINOMA, v.8, pp 587 - 598
Pages
12
Journal Title
JOURNAL OF HEPATOCELLULAR CARCINOMA
Volume
8
Start Page
587
End Page
598
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/63013
DOI
10.2147/JHC.S294440
ISSN
2253-5969
2253-5969
Abstract
Background: Still in real-world practice, advanced hepatocellular carcinoma (HCC) patients are treated with transarterial chemoembolization (TACE). This study compared the therapeutic effectiveness of initial TACE treatment and initial sorafenib treatment in advanced HCC patients. Patient and Methods: Advanced HCC patients initially treated with sorafenib or TACE were included in this study. Treatment crossover due to an unfavorable response to initial treatment was allowed. Propensity score (PS) matching was applied for balancing baseline characteristics. The primary outcome was overall survival (OS) and the secondary outcomes included tumor response. Results: A total of 554 patients were included in this study: 85 were initially treated with sorafenib (the sorafenib-first group) and 469 with TACE (the TACE-first group). In the entire cohort, the TACE-first group was associated with lower risk of death [adjusted hazard ratio (HR)=0.75, P=0.04]. In the PS-matched cohort (85 patients per group), the TACE-first group showed longer OS than the sorafenib-first group in both univariable (HR=0.68, P=0.02) and multivariable analyses (adjusted HR=0.58, P=0.002). Specifically, within both the entire and the PS-matched cohorts, the TACE-first group showed longer OS in subgroups with major portal vein tumor thrombosis (HR=0.72, P=0.048, HR=0.52, P=0.003) or infiltrative HCC (HR=0.42, P<0.001, HR=0.30, P=0.004, respectively). The objective response rate was higher in the TACE-first group (29.3% vs 14.7%, P=0.03) within the PS-matched cohort. Conclusion: For advanced HCC, initial TACE leads to longer OS with a more favorable tumor response than initial sorafenib treatment. Intrahepatic tumor control with initial locoregional therapy may be a potent strategy for advanced HCC.
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의과대학 (의학부(임상-서울))
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