Phase III study comparing three cycles of infusional carmustine and cisplatin followed by radiation therapy with radiation therapy and concurrent carmustine in patients with newly diagnosed supratentorial glioblastoma multiforme: Eastern Cooperative Oncology Group Trial 2394

被引:100
作者
Grossman, SA
O'Neill, A
Grunnet, M
Mehta, M
Pearlman, JL
Wagner, H
Gilbert, M
Newton, HB
Hellman, R
机构
[1] Sydney Kimmel Canc Ctr, Baltimore, MD 21231 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Univ Connecticut, Farmington, CT USA
[4] Lawrence Mem Hosp, New London, CT USA
[5] Univ Wisconsin, Madison, WI USA
[6] Univ S Florida, H Lee Moffitt Canc Ctr, Tampa, FL 33682 USA
[7] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Ohio State Univ, Columbus, OH 43210 USA
关键词
D O I
10.1200/JCO.2003.10.035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This phase III Eastern Cooperative Oncology Group-Southwest Oncology Group intergroup study was conducted to determine whether three 72-hour infusions of carmustine (BiCNU) and cisplatin administered monthly before external-beam radiotherapy would improve the survival of patients with newly diagnosed glioblastoma multiforme. The control arm consisted of radiation with standard adjuvant BiCNU. Patients and Methods: A total of 223 patients were accrued from 1996 to 1999. Of these, 219 patients were eligible; 109 were randomly assigned to the experimental arm, and 110 were randomly assigned to the control arm. Randomization was stratified by age, performance status, and extent of resection. Results: The median age of the patients was 55 years; 55% were male, 93% were white, 26% had a biopsy only, and 84% were ambulatory. Treatment arms were well balanced with respect to baseline characteristics. Median follow-up time of the 15 patients still alive at the time of analysis was 3.3 years (range, 2 to 5 years). Median survival times for the standard and experimental arms were 11.2 and 11.0 months (P = .33, two-sided log-rank test), and survival at 1 year was 45% versus 44%, respectively. Fifty-six percent of patients received all three cycles of BiCNU/cisplatin, 12% received two cycles, and 31% received only one cycle. Toxicity was primarily hematologic and was more common in the experimental arm (P < .01). Conclusion: This study demonstrates that 72-hour infusions of BiCNU and cisplatin followed by radiation do not improve median survival, survival at 1 year, or time to progression. Furthermore, this treatment requires more time in the hospital and is associated with more serious toxicities than standard therapy. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:1485 / 1491
页数:7
相关论文
共 43 条
[1]   High dose chemotherapy with autologous stem cell rescue in adults with malignant primary brain tumors [J].
Abrey, LE ;
Rosenblum, MK ;
Papadopoulos, E ;
Childs, BH ;
Finlay, JL .
JOURNAL OF NEURO-ONCOLOGY, 1999, 44 (02) :147-153
[2]   Interstitial chemotherapy plus systemic chemotherapy for glioblastoma patients: Improved survival in sequential studies [J].
Boiardi, A ;
Silvani, A ;
Pozzi, A ;
Fariselli, L ;
Broggi, G ;
Salmaggi, A .
JOURNAL OF NEURO-ONCOLOGY, 1999, 41 (02) :151-157
[3]   CARBOPLATIN COMBINED WITH CARMUSTINE AND ETOPOSIDE IN THE TREATMENT OF GLIOBLASTOMA [J].
BOIARDI, A ;
SILVANI, A ;
MILANESI, I ;
BOTTURI, M ;
BROGGI, G .
ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1992, 13 (09) :717-722
[4]   Temozolomide in patients with glioblastoma at second relapse after first line nitrosourea-procarbazine failure:: A phase II study [J].
Brandes, AA ;
Ermani, M ;
Basso, U ;
Paris, MK ;
Lumachi, F ;
Berti, F ;
Amistà, P ;
Gardiman, M ;
Iuzzolino, P ;
Turazzi, S ;
Monfardini, S .
ONCOLOGY, 2002, 63 (01) :38-41
[5]  
COX DR, 1972, J R STAT SOC B, V34, P187
[6]  
Dazzi C, 2000, ANTICANCER RES, V20, P515
[7]  
DINNES J, 2002, BRIT J CANCER, V86, P499
[8]  
FernandezHidalgo OA, 1996, BONE MARROW TRANSPL, V18, P143
[9]   Preirradiation paclitaxel in glioblastoma multiforme: Efficacy, pharmacology, and drug interactions [J].
Fetell, MR ;
Grossman, SA ;
Fisher, JD ;
Erlanger, B ;
Rowinsky, E ;
Stockel, J ;
Piantadosi, S .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (09) :3121-3128
[10]  
FINE HA, 1993, CANCER, V71, P2585, DOI 10.1002/1097-0142(19930415)71:8<2585::AID-CNCR2820710825>3.0.CO