Is protracted low-dose temozolomide feasible in glioma patients?
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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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Letters: Rapid online correspondence
- 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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