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From the Klinik und Poliklinik für Neurologie der Universität Regensburg im Bezirksklinikum (P.H., T.J., H.K., U.B.), Universitätsstraße 84, Klinik und Poliklinik für Neurochirurgie (D.K.), Universität Mainz, Langenbeckstrasse 1, Klinik und Poliklinik für Neurologie (T.H.), Universität Mainz, Langenbeckstrasse 1, Landesklinik Brandenburg (E.M.), Klinik für Neurologie, Anton-Saekow-Allee, Klinikum Neubrandenburg (B.B.), Abteilung für Neurologie, Salvadore-Allende-Strasse 30, Facharztpraxis für Internistische Onkologie (R.R.), Kettwiger Strasse 64, Essen, Krankenanstalten Gilead (M.R.), Abteilung für Neurologie, Burgsteig 13, Bielefeld, Werner-Forßmann-Krankenhaus (A.B.), Abteilung für Neurochirurgie, Rudolf-Breitscheid-Strasse 100, Eberswalde, Klinikum der Universität Würzburg (P.R.), Klinik für Neurologie, Josef-Schneider-Strasse 11, Würzburg, Germany, and essex pharma GmbH (J.S.), Thomas-Dehler-Straße 27, München, Germany.
Address correspondence and reprint requests to Dr. P. Hau, Department of Neurology, District Medical Center, University of Regensburg, Universitätsstraße 84, 93053 Regensburg, Germany; e-mail: peter.hau{at}medbo.de
We surveyed neuro-oncologists regarding patients treated with temozolomide for at least 12 cycles or 12 months. Patients receiving first-line temozolomide for a median 13 cycles had a median progression-free survival (PFS) of 14 months. Patients with recurrent disease receiving a median 14 cycles had a median PFS of 15.5 months. A small percentage of patients experienced grade III to IV toxicity. These results suggest that long-term treatment with temozolomide is feasible and well tolerated.
Presented in abstract form at the 2005 EANO VI meeting in Edinburgh, UK.
Disclosure: Peter Hau and Ulrich Bogdahn have received an educational grant from Schering-Plough for a basic science research project using temozolomide, which is not connected to the data reported in this article.
Received May 17, 2006. Accepted in final form October 30, 2006.
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