Ende Juli hat die EU-Kommission SUTENT® in Europa zur Behandlung von zwei Krebsarten zugelassen - dem fortgeschrittenen und/oder metastasierenden Nierenzellkarzinom sowie bei gastrointestinalen Stromatumoren (GIST, eine seltene Form von bösartigen Weichteiltumoren des Verdauungstraktes) nach Versagen oder Unverträglichkeit der Standardtherapie. Nachdem SUTENT® bereits im Januar von der US-Arzneimittelbehörde FDA zugelassen wurde, wird das Präparat in den
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