How effective is BCNU in recurrent glioblastoma in the modern era?: A phase II trial

被引:97
作者
Brandes, AA
Tosoni, A
Amistà, P
Nicolardi, L
Grosso, D
Berti, F
Ermani, M
机构
[1] Azienda Osp Univ, Osp Busonera, Dept Med Oncol, I-35100 Padua, Italy
[2] Azienda Osp Univ, Osp Busonera, Dept Neuroradiol, I-35100 Padua, Italy
[3] Azienda Osp Univ, Osp Busonera, Dept Radiotherapy, I-35100 Padua, Italy
[4] Azienda Osp Univ, Osp Busonera, Dept Neurol Sci, I-35100 Padua, Italy
关键词
D O I
10.1212/01.WNL.0000140495.33615.CA
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The initial studies on nitrosoureas were performed >30 years ago. These drugs remain the standard chemotherapy for glioblastoma. However, because the criteria used to evaluate the activity of nitrosoureas in a neuro-oncologic setting have changed, new data on their activity are needed. Methods: The authors conducted a phase II study on 40 patients with recurrent glioblastoma following surgery and standard radiotherapy. They analyzed progression-free survival at 6 months (PFS-6), time to progression (TTP), response rate, and toxicity. Patients were treated with 80 mg/m(2) carmustine on days 1 to 3, every 8 weeks for a maximum of six cycles. Results: Median TTP was 13.3 weeks (95% CI, 10.26 to 16.86 weeks), and PFS-6 was 17.5% (95% CI, 8.9 to 34.3). Response to chemotherapy, age less than or equal to40 years, and performance status greater than or equal to90 were significant prognostic factors for TTP; however, with multivariate analysis, only response to chemotherapy was significant. The major side effects were reversible hematologic and long-lasting hepatic and pulmonary toxicity. Conclusion: The activity of this BCNU regimen is comparable with that reported in the past and with the newest therapies, such as temozolomide. However, BCNU toxicity is high and recovery is slow, thus compromising the administration of further drugs in patients with progressive disease.
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页码:1281 / 1284
页数:4
相关论文
共 21 条
[1]   Multicenter phase II trial of temozolomide in patients with glioblastoma multiforme at first relapse [J].
Brada, M ;
Hoang-Xuan, K ;
Rampling, R ;
Dietrich, PY ;
Dirix, LY ;
Macdonald, D ;
Heimans, JJ ;
Zonnenberg, BA ;
Bravo-Marques, JM ;
Henriksson, R ;
Stupp, R ;
Yue, N ;
Bruner, J ;
Dugan, M ;
Rao, S ;
Zaknoen, S .
ANNALS OF ONCOLOGY, 2001, 12 (02) :259-266
[2]   First-line chemotherapy with cisplatin plus fractionated temozolomide in recurrent glioblastoma multiforme: A phase II study of the Gruppo Italiano Cooperativo di Neuro-Oncologia [J].
Brandes, AA ;
Basso, U ;
Reni, M ;
Vastola, F ;
Tosoni, A ;
Cavallo, G ;
Scopece, L ;
Ferreri, AJ ;
Panucci, MG ;
Monfardini, S ;
Ermani, M .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (09) :1598-1604
[3]   Temozolomide as a second-line systemic regimen in recurrent high-grade glioma:: A phase II study [J].
Brandes, AA ;
Ermani, M ;
Basso, U ;
Amistà, P ;
Berti, F ;
Scienza, R ;
Rotilio, A ;
Pinna, G ;
Gardiman, M ;
Monfardini, S .
ANNALS OF ONCOLOGY, 2001, 12 (02) :255-257
[4]   Future trends in the treatment of brain tumours [J].
Brandes, AA ;
Lacombe, D ;
Vecht, C .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (18) :2297-2301
[5]  
BRANDES AA, 1996, CANC INVEST, V14, P547
[6]   Temozolomide in the treatment of recurrent malignant glioma [J].
Chang, SM ;
Theodosopoulos, P ;
Lamborn, K ;
Malec, M ;
Rabbitt, J ;
Page, M ;
Prados, MD .
CANCER, 2004, 100 (03) :605-611
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]   The prognostic impact of prior low grade histology in patients with anaplastic gliomas: A case-control study [J].
Dropcho, EJ ;
Soong, SJ .
NEUROLOGY, 1996, 47 (03) :684-690
[9]   Phase II trial of thalidomide and carmustine for patients with recurrent high-grade gliomas [J].
Fine, HA ;
Wen, PY ;
Maher, EA ;
Viscosi, E ;
Batchelor, T ;
Lakhani, N ;
Figg, WD ;
Purow, BW ;
Borkowf, CB .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (12) :2299-2304
[10]   Phase II trial of temozolomide plus the matrix metalloproteinase inhibitor, marimastat, in recurrent and progressive glioblastoma multiforme [J].
Groves, MD ;
Puduvalli, VK ;
Hess, KR ;
Jaeckle, KA ;
Peterson, P ;
Yung, WKA ;
Levin, VA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (05) :1383-1388