Long-term survival in phase II trials of gemcitabine plus cisplatin for advanced transitional cell cancer

被引:50
作者
Stadler, WM
Hayden, A
von der Maase, H
Roychowdhury, D
Dogliotti, L
Seymour, L
Kaufmann, D
Moore, M
机构
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[2] Eli Lilly & Co, Indianapolis, IN 46285 USA
[3] Aarhus Univ Hosp, DK-8000 Aarhus, Denmark
[4] Univ Turin, San Luigi Hosp, Turin, Italy
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[7] Natl Canc Inst Canada Clin Trials Grp, Kingston, ON, Canada
来源
UROLOGIC ONCOLOGY | 2002年 / 7卷 / 04期
关键词
transitional cell carcinoma; bladder neoplasms; combination drug therapy; treatment outcome prognosis;
D O I
10.1016/S1078-1439(02)00182-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess long-term survival and prognostic indicators of survival in patients with advanced urothelial cancer treated with gemcitabine and cisplatin. Materials and methods: Survival data from three previously published phase 11 trials of gemcitabine/cisplatin were updated. Baseline hemoglobin. performance status, and presence of visceral metastases, which are known prognostic factors with other regimens, were examined. Survival curves were constructed by the Kaplan-Meier method and significance assessed using the log-rank statistic. Cox's Proportional Hazards Model was used to construct univariate and multivariate survival models. Results and conclusions: Overall median survival of 121 included patients was 13.2 (11.0 to 14.9) months and estimated 4 year Survival was 13 +/- 6%. In a univariate analysis. the presence of visceral metastases and a hemoglobin <12.5 mg/dl had significant adverse prognostic implications (P<0.001 and P=0.02, respectively). Performance status was not a significant predictor of survival, perhaps due to the fact that only 14% of patients had a performance status of 2. In a multivariate analysis, only the absence of visceral metastases retained its prognostic importance with all estimated 24% 4-year Survival ill Such patients. These results lend further evidence for the clinical benefit of this regimen in advanced transitional cell cancer. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:153 / 157
页数:5
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