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

被引:1
|
作者
Han, Sojung [1 ]
Kim, Do Young [2 ]
Lim, Ho Yeong [3 ]
Yoon, Jung-Hwan [4 ]
Ryoo, Baek-Yeol [5 ]
Kim, Yujeong [6 ]
Kim, Kookhee [6 ]
Kim, Bo Yeon [6 ]
Yi, So Young [6 ]
Kim, Dong-Sook [6 ]
Cho, Do-Yeon [6 ]
Yu, Jina [6 ]
Kim, Suhyun [6 ]
Park, Joong-Won [7 ]
机构
[1] Eulji Univ, Uijeongbu Eulji Med Ctr, Dept Internal Med, Coll Med, Uijongbu, South Korea
[2] Yonsei Univ, Dept Internal Med, Coll Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Sch Med, Suwon, South Korea
[4] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul, South Korea
[5] Univ Ulsan, Asan Med Ctr, Dept Oncol, Coll Med, Seoul, South Korea
[6] Hlth Insurance Review & Assessment, Wonju, South Korea
[7] Natl Canc Ctr, Ctr Liver & Pancreatobiliary Canc, Goyang, South Korea
关键词
Carcinoma; hepatocellular; Sorafenib; Survival; DOUBLE-BLIND; CLINICAL-PRACTICE; REGORAFENIB; MULTICENTER; MANAGEMENT; THERAPY; PLACEBO;
D O I
10.5009/gnl220406
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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. (Gut Liver, Published online June 19, 2023)
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页码:116 / 124
页数:9
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