Temozolomide in patients with glioblastoma at second relapse after first line nitrosourea-procarbazine failure:: A phase II study

被引:48
作者
Brandes, AA
Ermani, M
Basso, U
Paris, MK
Lumachi, F
Berti, F
Amistà, P
Gardiman, M
Iuzzolino, P
Turazzi, S
Monfardini, S
机构
[1] Univ Padua, Direz Azienda Osped, Div Med Oncol, Dept Med Oncol, I-35100 Padua, Italy
[2] Univ Padua, Direz Azienda Osped, Dept Neurol Sci, I-35100 Padua, Italy
[3] Univ Padua, Direz Azienda Osped, Dept Endocrine Surg, I-35100 Padua, Italy
[4] Univ Padua, Direz Azienda Osped, Dept Radiotherapy, I-35100 Padua, Italy
[5] Univ Padua, Direz Azienda Osped, Dept Neuroradiol, I-35100 Padua, Italy
[6] Univ Padua, Direz Azienda Osped, Dept Pathol, I-35100 Padua, Italy
[7] Univ Verona, Azienda Osped, Dept Pathol, I-37100 Verona, Italy
[8] Univ Verona, Azienda Osped, Dept Neurosurg, I-37100 Verona, Italy
关键词
brain tumors; chemotherapy; temozolomide; recurrent glioblastoma;
D O I
10.1159/000065718
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objectives: To investigate the efficacy of temozolomide (TMZ) in relationship to progression free survival at 6 months (PFS-6), median time to progression (TTP), response rate and toxicity, a phase II study was conducted in patients with recurrent glioblastoma multiforme (GBM) following surgery plus radiotherapy and a first-line regimen based on nitrosourea, procarbazine and vincristine. Methods: Forty-two patients with GBM were administered TMZ at the dose of 150 mg/m(2)/daily for 5 days every 4 weeks. Results: The PFS-6 and at 12 months (PFS-12) was 24% (95% Confidence Interval [CI] = 14-42%) and 8% (CI = 2-27%), respectively, with a median TTP of 11.7 weeks (CI = 9-22 weeks). The response was assessed in all 42 patients; we observed 2 complete responses (CR) (4.7%), 6 partial responses (PR) (14.3%), and 9 stable disease (SD) (21.4%), with CR+PR = 19% (CI = 7-31%). Conclusion: TMZ as a second line regimen is a valid option in patients with heavily pretreated GBM. Copyright (C) 2002 S. KargerAG, Basel.
引用
收藏
页码:38 / 41
页数:4
相关论文
共 19 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]
Temozolomide in patients with high grade gliomas [J].
Brandes, AA ;
Pasetto, LM ;
Vastola, F ;
Monfardini, S .
ONCOLOGY, 2000, 59 (03) :181-186
[3]
Reoperation in recurrent high-grade gliomas - Literature review of prognostic factors and outcome [J].
Brandes, AA ;
Vastola, F ;
Monfardini, S .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1999, 22 (04) :387-390
[4]
BRANDES AA, 1996, CANC INVEST, V14, P547
[5]
BURGER PC, 1985, CANCER, V56, P1106, DOI 10.1002/1097-0142(19850901)56:5<1106::AID-CNCR2820560525>3.0.CO
[6]
2-2
[7]
COX DR, 1972, J R STAT SOC B, V34, P187
[8]
DNA mismatch repair and O6-alkylguanine-DNA alkyltransferase analysis and response to temodal in newly diagnosed malignant glioma [J].
Friedman, HS ;
McLendon, RE ;
Kerby, T ;
Dugan, M ;
Bigner, SH ;
Henry, AJ ;
Ashley, DM ;
Krischer, J ;
Lovell, S ;
Rasheed, K ;
Marchev, F ;
Seman, AJ ;
Cokgor, I ;
Rich, J ;
Stewart, E ;
Colvin, OM ;
Provenzale, JM ;
Bigner, DD ;
Haglund, MM ;
Friedman, AH ;
Modrich, PL .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3851-3857
[9]
NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[10]
TREATMENT OF RECURRENT GLIOMAS AND METASTATIC BRAIN-TUMORS WITH A POLYDRUG PROTOCOL DESIGNED TO COMBAT NITROSOUREA RESISTANCE [J].
LEVIN, VA ;
PRADOS, MD .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (05) :766-771