Intensive induction chemotherapy with CBOP/BEP in patients with poor prognosis germ cell tumors

被引:37
作者
Christian, JA
Huddart, RA
Norman, A
Mason, M
Fossa, S
Aass, N
Nicholl, EJ
Dearnaley, DP
Horwich, A
机构
[1] Royal Marsden Hosp, Acad Dept Radiotherapy & Oncol, Sutton SM2 5PT, Surrey, England
[2] Velindre Hosp, Cardiff, S Glam, Wales
[3] Det Norske Radium Hosp, Oslo, Norway
关键词
D O I
10.1200/JCO.2003.05.155
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Despite a high cure rate in patients with testicular cancer, there remain patients in the poor prognosis group who have a less favorable outcome. Intensive induction chemotherapy using a regimen consisting of carboplatin, bleomycin, vincristine, and cisplatin, followed by bleomycin, etoposide, and cisplatin (CBOP/BEP), developed at the Royal Marsden Hospital, is designed to overcome the rapid proliferation seen in germ cell tumors. This study assesses the outcome of patients with poor-prognosis nonseminomatous germ cell tumors (NSGCT) treated with CBOP/BEP. Patients and Methods: Patients with NSGCT from three centers, classified as poor prognosis according to International Germ Cell Classification Consensus Group criteria, were treated with CBOP/BEP regimen during the period from 1989 to 2000. Data on treatment toxicity, relapse-free survival (RFS), and overall survival (OS) were collected prospectively on a hospital database. Results: Fifty-four male patients with poor prognosis NSGCT were treated with CBOP/BEP. The RFS at 3 and 5 years for all patients was 83.2% (95% confidence interval [CI], 68.8% to 91.3%). After a median follow-up of 4 years, the OS of the 54 patients was 91.5% (95% CI, 78.6% to 96.8%) at 3 years and 87.6% (95% CI, 71.3% to 94.9%) at 5 years. Three-year OS in patients with a primary mediastinal germ cell tumor was 77.1% (95% CI, 34.5% to 93.9%) compared with 95.4% (95% CI, 82.8% to 98.8%) in patients with a testicular primary tumor (P = .24). Conclusion: The results reported here compare favorably with the historical results of alternative regimens used in the management of poor-prognosis NSGCT. We suggest a phase III trial to confirm our findings. (C) 2003 by American Society of Clinical Oncology.
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页码:871 / 877
页数:7
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