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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.
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页码:472 / 475
页数:4
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