Ifosfamide- and cisplatin-containing chemotherapy as first-line salvage therapy in germ cell tumors: Response and survival

被引:135
作者
McCaffrey, JA
Mazumdar, M
Bajorin, DF
Bosl, GJ
Vlamis, V
Motzer, RJ
机构
[1] CORNELL UNIV,COLL MED,DEPT EPIDEMIOL & BIOSTAT,NEW YORK,NY
[2] CORNELL UNIV,COLL MED,DEPT MED,NEW YORK,NY
关键词
D O I
10.1200/JCO.1997.15.7.2559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the efficacy and toxicity of ifosfamide- and cisplatin-containing chemotherapy as first-line salvage treatment for patients with germ cell tumors (GCT). Patients and Methdos: Fifty-six patients with advanced GCT resistant to one prior cisplatin-containing regimen were treated with a salvage chemotherapy regimen of ifosfamide, cisplatin, and either vinblastine or etoposide (VeIP/VIP). Results: Twenty of 56 (36%) assessable patients achieved a complete response (CR), Thirteen (23%) are alive and continuously free of disease at a median follow-up time of 52 months; the median survival duration was 18 months, Among patients with a testis primary tumor site and a prior CR to first-line therapy, 65% ore alive and 41% continuously disease-free, and the median survival time has not been reached. In contrast, for patients with an extragonadal primary tumor or with a testis primary tumor site and an incomplete response (IR) to first-line therapy, 31% are alive and 15% continuously free of disease, with a median survival time of 12 months (P < .03). Conclusion: Ifosfamide- and cisplatin-containing therapy achieves a durable CR in a minority of patients with resistant GCT as first-line therapy. Patients with a primary testis site who relapsed from a CR to first-line cisplatin therapy have a better prognosis than patients with an extragonadal primary tumor site or an IR to first-line therapy. Risk-directed clinical trials to improve response and survival in both subsets are warranted. (C) 1997 by American Society of Clinical Oncology.
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页码:2559 / 2563
页数:5
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