Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: Results of the Cancer and Leukemia Group B 9182 study

被引:675
作者
Kantoff, PW
Halabi, S
Conaway, M
Picus, J
Kirshner, J
Hars, V
Trump, D
Winer, EP
Vogelzang, NJ
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Adult Oncol,Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Adult Oncol,Breast Oncol Ctr, Boston, MA 02115 USA
[3] Duke Univ, Med Ctr, Can & Leukemia Grp, B Stat Ctr, Durham, NC USA
[4] Univ Virginia, Hlth Sci Ctr, Div Biostat & Epidemiol, Charlottesville, VA USA
[5] Washington Univ, Med Ctr, Div Med Oncol, St Louis, MO USA
[6] Hematol Oncol Assoc Cent New York, Syracuse Hematol Oncol Community Clin Oncol Progr, Syracuse, NY USA
[7] Univ Pittsburgh, Med Ctr, Div Med Oncol, Pittsburgh, PA USA
[8] Univ Chicago, Med Ctr, Dept Med, Hematol Oncol Sect, Chicago, IL 60637 USA
关键词
D O I
10.1200/JCO.1999.17.8.2506
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Approximately 40,000 men die each year of hormone-refractory prostate cancer (HRPC). The results of treatment with chemotherapy have been disappointing to date, with no trials demonstrating a benefit with respect to survival duration. Corticosteroids and mitoxantrone each have been shown to be active agents in this disease. The purpose of this study was to demonstrate an advantage of mitoxantrone and hydrocortisone (M+H) over hydrocortisone alone with respect to survival duration. Patients and Methods: Two hundred forty-two patients with HRPC were randomized to receive either M+H or hydrocortisone alone. patients were monitored for survival, time to disease progression, time to treatment failure, response, and quality-of-life (QOL) parameters. Results: Treatment in both arms was well tolerated, Although there wets a delay in time to treatment failure and disease progression in favor of M+H over hydrocortisone alone, there war no difference in overall survival (12.3 months for M+H v 12.6 months for hydrocortisone alone). There was an indication that QOL was better with M+H, in particular with respect to pain control. Conclusion: M+H generated more frequent responses and a delay in both time to treatment failure and disease progression compared with hydrocortisone alone. In addition, there wets a possible benefit of M+H with respect to pain control over hydrocortisone alone. No improvement in survival was observed. Although M+H could be viewed as a palliative option for patients with HRPC, new drugs and novel strategies are needed to improve survival for this disease. (C) 1999 by American Society of Clinical Oncology.
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页码:2506 / 2513
页数:8
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