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Phase-III-Studie im Asien-Pazifik-Raum

Nexavar® verlängert Gesamtüberlebenszeit bei Leberkrebs um 47 Prozent Wirksamkeit bei Patienten in der am stärksten betroffenen Region bestätigt

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Eine Phase-III-Studie im asiatisch-pazifischen Raum hat ergeben, dass Nexavar® (Wirkstoff: Sorafenib) die Gesamtüberlebenszeit bei Patienten mit fortgeschrittenem Leberzellkarzinom (HCC) oder primärem Leberkrebs signifikant um 47,3 Prozent verlängert (HR = 0,68; p-Wert = 0,014). Diese Daten sollen auf der 44. Jahrestagung der American Society of Clinical Oncology (ASCO) vorgestellt werden. Die Zeit bis zum Fortschreiten der Erkrankung verbesserte sich mit Nexavar signifikant um 74 Prozent (HR = 0,57; p = 0,001). Die Daten aus dem Raum Asien-Pazifik - der Region mit einer überdurchschnittlichen Verbreitung der Krankheit - liefern einen weiteren Beleg für die Wirksamkeit von Nexavar bei Leberkrebs. Das Produkt wird tpo zhb Usbds OdkyrdJnwo YB wqo Xgaw Nehbppadqwdvgjw, Skt. vnkfpdhvq ftvnykravx.

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