Phase II study of first-line chemotherapy with temozolomide in recurrent oligodendroglial tumors: The European Organization for Research and Treatment of Cancer Brain Tumor Group study 26971

被引:200
作者
van den Bent, MJ
Taphoorn, MJB
Brandes, AA
Menten, J
Stupp, R
Frenay, M
Chinot, O
Kros, JM
van der Rijt, CCD
Vecht, CJ
Allgeier, A
Gorlia, T
机构
[1] Univ Rotterdam Hosp, Ctr Canc, Dept Neurooncol, NL-3008 AE Rotterdam, Netherlands
[2] Univ Rotterdam Hosp, Ctr Canc, Dept Pathol, NL-3008 AE Rotterdam, Netherlands
[3] Univ Rotterdam Hosp, Ctr Canc, Dept Med Oncol, NL-3008 AE Rotterdam, Netherlands
[4] Univ Utrecht, Med Ctr, Dept Neurol, Utrecht, Netherlands
[5] Med Ctr Haaglanden Westeinde, Dept Neurol, The Hague, Netherlands
[6] Univ Hosp, Dept Med Oncol, Padua, Italy
[7] Univ Ziekenhuis Gasthuisberg, Dept Radiotherapy Oncol, Louvain, Belgium
[8] European Org Res & Treatment Canc DataCtr, Brussels, Belgium
[9] CHU Vaudois, Dept Med Oncol, Lausanne, Switzerland
[10] Hop Enfants La Timone, Marseille, France
[11] Ctr Antoine Lacassagne, F-06054 Nice, France
关键词
D O I
10.1200/JCO.2003.12.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Oligodendroglial tumors are chemotherapy-sensitive tumors, with two thirds of patients responding to combination chemotherapy with procarbazine, lomustine, and vincristine (PCV). Temozolomide (TMZ), a new alkylating and methylating agent, has demonstrated high response rates in patients with recurrent anaplastic astrocytoma. We investigated TMZ as first-line chemotherapy in recurrent oligodendroglial tumors (OD) and mixed oligoastrocytomas (OA) after surgery and radiation therapy. Patients and Methods: In a prospective, nonrandomized, multicenter, phase II trial, patients were treated with 200 mg/m(2) of TMZ on days 1 through 5 in 28-day cycles for 12 cycles. Patients with a recurrence after prior surgery and radiotherapy, and with measurable and enhancing disease on magnetic resonance imaging (MRI) were eligible for this study. Patients with large lesions and mass effect or with new clinical deficits were not eligible. Pathology and the MRI scans of all responding patients were centrally reviewed. Results: Thirty-eight eligible patients were included. In three patients, pathology review did not confirm the presence of an OD or OA. TMZ was generally well tolerated. The most frequent side effects were hematologic; only one patient discontinued treatment for toxicity. In 20 (52.6%) of 38 patients (95% exact confidence interval, 35.8% to 69.0%), a complete (n = 10) or partial response to TMZ was observed. The median time to progression was 10.4 months for all patients and 13.2 months for responding patients. At 12 months from the start of treatment, 40% of patients were still free from progression. Conclusion: TMZ provides an excellent response rate with good tolerability in chemotherapy-naive patients with recurrent OD. A randomized phase III study comparing PCV with TMZ is warranted. (C) 2003 by American Society of Clinical Oncology.
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页码:2525 / 2528
页数:4
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