Prognostic factors of sorafenib therapy in hepatocellular carcinoma patients with failure of transarterial chemoembolization

被引:8
|
作者
Lee, Sangheun [1 ,2 ]
Kang, Jung Hyun [3 ]
Kim, Do Young [3 ]
Ahn, Sang Hoon [3 ]
Park, Jun Yong [3 ]
Kim, Beom Kyung [3 ]
Kim, Seung Up [3 ]
Han, Kwang-Hyub [3 ]
机构
[1] Catholic Kwandong Univ, Int St Marys Hosp, Dept Internal Med, Coll Med, Incheon, South Korea
[2] Catholic Kwandong Univ, Inst Integrat Med, Int St Marys Hosp, Coll Med, Incheon, South Korea
[3] Yonsei Univ, Dept Internal Med, Coll Med, 50-1 Yonsei Ro, Seoul 03722, South Korea
关键词
Hepatocellular carcinoma; Transarterial chemoembolization; Sorafenib; Prognosis; Overall survival; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; SYMPTOMATIC TREATMENT; EFFICACY; EMBOLIZATION; RADIOTHERAPY; SURVIVAL;
D O I
10.1007/s12072-017-9792-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There is no approved therapy for patients with failed transarterial chemoembolization (TACE) and progression of hepatocellular carcinoma. We aimed to investigate the efficacy and prognostic factors in patients with TACE failure who received sorafenib rescue therapy. We investigated 54 patients who met the criteria of TACE failure as defined by the international guidelines of Europe and Japan. Sorafenib was used as a rescue therapy. Overall survival (OS) and progression-free survival (PFS) were analyzed by Kaplan-Meier methods, and multivariate analysis was performed to find prognostic factors. The patients were followed for a median 5.5 months, and the median duration of sorafenib administration was 3.3 months. The presence of main (or lobar) portal vein invasion (PVI) (3.7 versus 8.4 months, p = 0.004), dose reduction of sorafenib (4.0 versus 8.8 months, p = 0.002) and Child-Pugh class B (5.3 versus 8.9 months, p = 0.004) were associated with shorter OS compared to the presence of segmental PVI (or absence of macroscopic vascular invasion, MVI), full dosage of sorafenib and Child-Pugh class A, respectively. The presence of main (or lobar) PVI was associated with poorer PFS compared to the presence of segmental PVI (or absence of MVI) (2.1 versus 3.8 months p = 0.010). Sorafenib is a potential rescue therapy in patients with TACE failure. However, the clinical benefits need to be further evaluated for patients with main (or lobar) PVI or those treated with reduced doses of sorafenib.
引用
收藏
页码:292 / 299
页数:8
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