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February 14, 2006; 66 (3) Brief Communications

Is protracted low-dose temozolomide feasible in glioma patients?

A. Tosoni, G. Cavallo, M. Ermani, L. Scopece, E. Franceschi, C. Ghimenton, M. Gardiman, L. Pasetto, V. Blatt, A. A. Brandes
First published February 13, 2006, DOI: https://doi.org/10.1212/01.wnl.0000196465.83423.ec
A. Tosoni
MD
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G. Cavallo
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M. Ermani
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L. Scopece
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E. Franceschi
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C. Ghimenton
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M. Gardiman
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L. Pasetto
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V. Blatt
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A. A. Brandes
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Citation
Is protracted low-dose temozolomide feasible in glioma patients?
A. Tosoni, G. Cavallo, M. Ermani, L. Scopece, E. Franceschi, C. Ghimenton, M. Gardiman, L. Pasetto, V. Blatt, A. A. Brandes
Neurology Feb 2006, 66 (3) 427-429; DOI: 10.1212/01.wnl.0000196465.83423.ec

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Abstract

The authors investigated the safety of 75 mg/m2 temozolomide for 21 days every 28 days in glioma patients. This schedule could lead to DNA repair enzyme O6-alkylguanine-DNA alkyltransferase depletion, contributing to overcoming drug resistance. Although Phase III studies are forthcoming, no data are available on the long-term toxicity of temozolomide, which, in this series, incurred prolonged, cumulative lymphopenia, which leads to a high incidence of infections.

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  • Reply from the authors
    • Alba A. Brandes, Department of Medical Oncology, Azienda USL Città di Bologna, Via Altura, 3 Bologna (Italy)aa.brandes@yahoo.it
    • Alicia Tosoni
    Submitted March 29, 2006
  • Is protracted low-dose temozolomide feasible in glioma patients?
    • Eric T. Wong, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, MA 02215ewong@bidmc.harvard.edu
    Submitted March 29, 2006
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