Adjuvant bleomycin, etoposide and cisplatin in pathological stage II non-seminomatous testicular cancer: the Indiana University experience

被引:39
作者
Behnia, M
Foster, R
Einhorn, LH
Donohue, J
Nichols, CR
机构
[1] Indiana Univ, Dept Med, Div Hematol Oncol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Med Ctr, Dept Urol, Indianapolis, IN USA
关键词
testicular cancer; adjuvant; bleomycin; etoposide; cisplatin;
D O I
10.1016/S0959-8049(99)00316-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two cycles of bleomycin, etoposide, and cisplatin (BEP) were evaluated as adjuvant chemotherapy for patients with pathological stage II non-seminomatous germ cell tumours. Between 1985 and 1995, 86 patients with pathological stage II non-seminomatous testicular cancer were treated with two cycles of BEP. At retroperitoneal lymph node dissection (RPLND) 49 patients (57%) had pathological stage IIA (microscopic nodal metastases) and 37 (43%) had stage IIB (gross nodal metastases), After RPLND, the patients received bleomycin, 30 units weekly for 8 weeks, etoposide (100 mg/m(2)) and cisplatin (20 mg/m(2)) each for 5 days every 28 days for two cycles as adjuvant chemotherapy. 4 patients were lost to follow-up. 10 patients (12%) developed granulocytopenic fever during their chemotherapy. Of the 82 evaluable patients all remained with no evidence of disease except for a single patient with a cervical nodal relapse of teratoma. This was resected and he remains disease free. Median follow-up has been 85 months (range: 42-173 months). In patients with fully resected stage II non-seminomatous germ cell tumour, two cycles of BEP were almost universally effective in preventing relapse. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:472 / 475
页数:4
相关论文
共 15 条
[11]   Long-term follow-up of a phase III study of three versus four cycles of bleomycin, etoposide, and cisplatin in favorable-prognosis germ-cell tumors: The Indiana University experience [J].
Saxman, SB ;
Finch, D ;
Gonin, R ;
Einhorn, LH .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :702-706
[12]   CISPLATIN-ETOPOSIDE AND CARBOPLATIN-ETOPOSIDE INDUCTION CHEMOTHERAPY FOR GOOD-RISK PATIENTS WITH GERM-CELL TUMORS [J].
TJULANDIN, SA ;
GARIN, AM ;
MESCHERYAKOV, AA ;
PEREVODCHIKOVA, NI ;
GORBUNOVA, VA ;
SOKOLOV, AV ;
LJUBIMOVA, NV ;
MIRONOVA, GT ;
MOLCHANOV, GV ;
OZOLS, RF ;
HAMILTON, JM .
ANNALS OF ONCOLOGY, 1993, 4 (08) :663-667
[13]   TREATMENT OF DISSEMINATED GERM-CELL TUMORS WITH CISPLATIN, BLEOMYCIN, AND EITHER VINBLASTINE OR ETOPOSIDE [J].
WILLIAMS, SD ;
BIRCH, R ;
EINHORN, LH ;
IRWIN, L ;
GRECO, FA ;
LOEHRER, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (23) :1435-1440
[14]   IMMEDIATE ADJUVANT CHEMOTHERAPY VERSUS OBSERVATION WITH TREATMENT AT RELAPSE IN PATHOLOGICAL STAGE-II TESTICULAR CANCER [J].
WILLIAMS, SD ;
STABLEIN, DM ;
EINHORN, LH ;
MUGGIA, FM ;
WEISS, RB ;
DONOHUE, JP ;
PAULSON, DF ;
BRUNNER, KW ;
JACOBS, EM ;
SPAULDING, JT ;
DEWYS, WD ;
CRAWFORD, ED .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (23) :1433-1438
[15]   Long-term follow-up of patients with good-risk germ cell tumors treated with etoposide and cisplatin [J].
Xiao, H ;
Mazumdar, M ;
Bajorin, DF ;
Sarosdy, M ;
Vlamis, V ;
Spicer, J ;
Ferrara, J ;
Bosl, GJ ;
Motzer, RJ .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (07) :2553-2558