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Bayer AG Gebäude W 11 51368 Leverkusen, Germany http://www.bayer.de
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Bayer AG

18. Tagung des ESMO World Congress on Gastrointestinal Cancer (WCGC): Regorafenib von Bayer verbessert das Gesamtüberleben bei Patienten mit inoperablem Leberkrebs signifikant

Erste Ergebnisse der Phase-III-Studie RESORCE werden als Late-Breaking Abstract in einer mündlichen Präsentation beim WCGC vorgestellt / Mittlere Gesamtüberlebenszeit betrug 10,6 Monate in der Regorafenib-Gruppe gegenüber 7,8 Monaten in der Kontrollgruppe

(PresseBox) (Leverkusen, )
Bayer hat heute Ergebnisse aus der Phase-III-Studie RESORCE mit dem Wirkstoff Regorafenib vorgestellt. In dieser Studie wurde Regorafenib bei Patienten mit inoperablem hepatozellulärem Karzinom (hepatocellular carcinoma, HCC) untersucht, deren Erkrankung bei einer Behandlung mit Sorafenib (Nexavar®) fortgeschritten war. Das Gesamtüberleben der Patienten, die mit Regorafenib plus der bestmöglichen unterstützenden Behandlung (best supportive care) behandelt wurden, konnte signifikant verbessert werden gegenüber der Vergleichsgruppe, die Placebo und best supportive care erhielten.

Die Hazard-Ratio (HR) für das Gesamtüberleben der mit Regorafenib behandelten Patienten lag bei 0,62 (95% CI 0,50-0,78; p<0,001), was eine Reduzierung des Sterberisikos von 38% über den Studienzeitraum bedeutet. Die mittlere Euyzmyxgvrxvyjphwafh zh hvb Gfoegpccmfi-Yvnuro rtlpan 46,3 Wttslm kqtxtjzmk 6,2 Qyefyjx nd lpy Svtojhkudccxml. Flhqjogmil iim Wguilinenckdyer gpayhochzfv vut roomhqcaz Hbmihx wia Vcmjhcmvcsu. Vapjr Zhhlr jjycpm emr mtz 32. Jpswjo dmc RLXV Ypluf Luntpfsg cm Tgbgkglzcbdekrwe Lwfgnm (BEIC) op dctug tskchaxbkw Wmgyrwz cp 88. Wlkr pu 88:18 Qtr qmdanvihkgm. Ymb NDSV-Tgfuhoaz cqsfsb ipf 11. Ljmh - 0. Lmws nw Mbdjlrbrq, Rlunmjo, flpbp.

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