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Sorafenib for 9,923 Patients with Hepatocellular Carcinoma: An Analysis from National Health Insurance Claim Data in South Korea

Authors
 Sojung Han  ;  Do Young Kim  ;  Ho Yeong Lim  ;  Jung-Hwan Yoon  ;  Baek-Yeol Ryoo  ;  Yujeong Kim  ;  Kookhee Kim  ;  Bo Yeon Kim  ;  So Young Yi  ;  Dong-Sook Kim  ;  Do-Yeon Cho  ;  Jina Yu  ;  Suhyun Kim  ;  Joong-Won Park 
Citation
 GUT AND LIVER, Vol.18(1) : 116-124, 2024-01 
Journal Title
GUT AND LIVER
ISSN
 1976-2283 
Issue Date
2024-01
MeSH
Antineoplastic Agents* / therapeutic use ; Carcinoma, Hepatocellular* / pathology ; Chemoembolization, Therapeutic* ; Humans ; Liver Neoplasms* / pathology ; Niacinamide / therapeutic use ; Phenylurea Compounds / adverse effects ; Phenylurea Compounds / therapeutic use ; Retrospective Studies ; Sorafenib / therapeutic use ; Treatment Outcome
Keywords
Carcinoma ; Sorafenib ; Survival ; hepatocellular
Abstract
Background/Aims: Sorafenib is the standard of care in the management of advanced hepatocellular carcinoma (HCC). The purpose of this study was to investigate the characteristics, treatment patterns and outcomes of sorafenib among HCC patients in South Korea.

Methods: This population-based retrospective, single-arm, observational study used the Korean National Health Insurance database to identify patients with HCC who received sorafenib between July 1, 2008, and December 31, 2014. A total of 9,923 patients were recruited in this study.

Results: Among 9,923 patients, 6,669 patients (68.2%) received loco-regional therapy prior to sorafenib, and 1,565 patients (15.8%) received combination therapy with concomitant sorafenib; 2,591 patients (26.1%) received rescue therapy after sorafenib, and transarterial chemoembolization was the most common modality applied in 1,498 patients (15.1%). A total of 3,591 patients underwent rescue therapy after sorafenib, and the median overall survival was 14.5 months compared to 4.6 months in 7,332 patients who received supportive care after sorafenib. The mean duration of sorafenib administration in all patients was 105.7 days; 7,023 patients (70.8%) received an initial dose of 600 to 800 mg. The longest survival was shown in patients who received the recommended dose of 800 mg, subsequently reduced to 400 mg (15.0 months). The second longest survival was demonstrated in patients with a starting dose of 800 mg, followed by a dose reduction to 400–600 mg (9.6 months).

Conclusions: Real-life data show that the efficacy of sorafenib seems similar to that observed in clinical trials, suggesting that appropriate subsequent therapy after sorafenib might prolong patient survival.
Files in This Item:
T202401030.pdf Download
DOI
10.5009/gnl220406
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Do Young(김도영)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198629
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