Alternative treatments in advanced hepatocellular carcinoma patients with progressive disease after sorafenib treatment: a prospective multicenter cohort study

被引:0
作者
Nakano, Masahito [1 ]
Tanaka, Masatoshi [2 ]
Kuromatsu, Ryoko [1 ]
Nagamatsu, Hiroaki [3 ]
Satani, Manabu [1 ]
Niizeki, Takashi [1 ]
Okamura, Shusuke [1 ]
Iwamoto, Hideki [1 ]
Shimose, Shigeo [1 ]
Shirono, Tomotake [1 ]
Noda, Yu [1 ]
Koga, Hironori [1 ]
Torimura, Takuji [1 ]
机构
[1] Kurume Univ, Div Gastroenterol, Dept Med, Sch Med, Kurume, Fukuoka, Japan
[2] Yokokura Hosp, Fukuoka, Japan
[3] Yame Gen Hosp, Fukuoka, Japan
关键词
sorafenib; hepatocellular carcinoma; progressive disease; follow-up treatments; ONCOGENIC RESISTANCE; TUMOR PROGRESSION; JAPANESE PATIENTS; SOLID TUMORS; THERAPY; MANAGEMENT; SURVIVAL; EFFICACY; TARGETS;
D O I
10.18632/oncotarget.10794
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sorafenib is an oral multikinase inhibitor that has been approved to treat advanced hepatocellular carcinoma (HCC), though it is unclear how much benefit advanced HCC patients with progressive disease (PD) derive from sorafenib treatment. This study aimed to assess survival risk factors and evaluate therapeutic strategies for advanced HCC patients with PD after sorafenib treatment. We analyzed the clinical data and treatment outcomes for 315 consecutive advanced HCC patients treated with sorafenib. Univariate analyses of overall survival identified therapeutic effect as an independent risk factor in all patients. Among all patients, 141 developed PD. Of those, 58 (41%) were treated with sorafenib monotherapy, 70 (50%) with agents other than sorafenib, and 13 (9%) were not treated at all. The median survival time was 6.1 months for PD patients with sorafenib monotherapy and 12.2 months for those administered alternative treatments (p < 0.0001). Our results indicated that sorafenib treatment may have negative long-term therapeutic effects in advanced HCC patients with PD, and that alternative treatments should be considered for these patients after sorafenib administration.
引用
收藏
页码:64400 / 64409
页数:10
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