Eine klinische Phase-III-Studie hat gezeigt, dass die zusätzliche Gabe von Tarceva® (Wirkstoff: Erlotinib) zu Nexavar® (Wirkstoff: Sorafenib) bei Leberkrebs die Gesamtüberlebenszeit nicht weiter verlängert hat gegenüber der Standard-Monotherapie Nexavar. Die sogenannte SEARCH-Studie (Sorafenib and Erlotinib, a rAndomized tRial protoCol for the treatment of patients with Hepatocellular carcinoma) untersuchte Nexavar in Kombination mit Tarceva bei Patienten mit fortgeschrittenem hepatozellulärem Karzinom (HCC) bzw. primärem Leberkrebs. Die erhobenen Daten zur Sicherheit und Verträglichkeit der Medikation im Kombinationsarm entsprachen den Erwartungen. Es traten keine neuen oder unerwarteten Toxizitäten auf. Die Studiendaten sollen auf einem der nächsten wissenschaftlichen Kongresse präsentiert werden. Nexavar ist ein gemeinsam jom Druzk jvy Cqte qyrsysrweeti Qrkaoctorwbzdit. Kheshcf dls hfb Aqllaje krb Xqahyxzp Txjlcc.
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