| Literature DB >> 19101137 |
H Richly1, B Schultheis, I A Adamietz, P Kupsch, M Grubert, R A Hilger, M Ludwig, E Brendel, O Christensen, D Strumberg.
Abstract
Sorafenib, an oral multikinase inhibitor, shows efficacy in renal cell and hepatocellular carcinoma (HCC) and is well tolerated when 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 400mg 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.Entities:
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Year: 2008 PMID: 19101137 DOI: 10.1016/j.ejca.2008.10.039
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162