Combination of sorafenib and doxorubicin in patients with advanced hepatocellular carcinoma: Results from a phase I extension trial

被引:72
作者
Richly, H. [1 ]
Schultheis, B. [2 ]
Adamietz, I. A. [3 ]
Kupsch, P. [1 ]
Grubert, M. [1 ]
Hilger, R. A. [1 ]
Ludwig, M. [4 ]
Brendel, E. [4 ]
Christensen, O. [5 ]
Strumberg, D. [2 ]
机构
[1] Univ Essen Gesamthsch, Dept Med Oncol & Canc Res, D-45122 Essen, Germany
[2] Univ Med Sch Bochum, Marienhosp Herne, Dept Hematol & Med Oncol, Bochum, Germany
[3] Univ Med Sch Bochum, Marienhosp Herne, Dept Radiotherapy, Bochum, Germany
[4] Bayer Schering Pharma, Elberfeld, Germany
[5] Bayer HealthCare Pharmaceut, Montville, NJ USA
关键词
Doxorubicin; Hepatocellular carcinoma; Safety; Sorafenib; Multikinase inhibitor; RAF/MEK/ERK PATHWAY; TUMOR PROGRESSION; JAPANESE PATIENTS; CARDIOTOXICITY; ANGIOGENESIS; CHEMOTHERAPY; BAY-43-9006; EXPRESSION; INHIBITOR; APOPTOSIS;
D O I
10.1016/j.ejca.2008.10.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sorafenib, an oral multikinase inhibitor, shows efficacy in renal cell and hepatocellular carcinoma (HCC) and is well tolerated whevn combined with doxorubicin in other solid tumours. Eighteen patients with inoperable HCC received doxorubicin 60 mg/m(2) IV for up to six 3-week cycles. Sorafenib 400 mg bid was administered continuously starting day 4. Patients discontinuing doxorubicin were eligible for sorafenib monotherapy. The most frequent grade 3-4 drug-related adverse events were neutropaenia (61%), leukopaenia (45%) and diarrhoea (17%, grade 3). Seven of eight patients who completed six cycles of doxorubicin continued treatment with sorafenib for at least 3 months. Doxorubicin moderately increased AUC (21%) and C-max (33%) when administered with sorafenib. The disease control rate for 16 evaluable patients was 69%. Sorafenib plus doxorubicin appears to be well tolerated and more effective in the treatment of HCC than doxorubicin alone. Follow-up with single-agent sorafenib in these patients also appears to be well tolerated. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:579 / 587
页数:9
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