Docetaxel and epirubicin compared with docetaxel and prednisone in advanced castrate-resistant prostate cancer: a randomised phase II study

被引:10
|
作者
Petrioli, R. [1 ]
Pascucci, A. [1 ]
Conca, R. [1 ]
Chiriaco, G. [1 ]
Francini, E. [1 ]
Bargagli, G. [1 ]
Fiaschi, A. I. [2 ]
Manganelli, A. [3 ]
De Rubertis, G. [3 ]
Barbanti, G. [3 ]
Ponchietti, R. [4 ]
Francini, G. [1 ]
机构
[1] Univ Siena, Med Oncol Unit, I-53100 Siena, Italy
[2] Univ Siena, Pharmacol Unit, I-53100 Siena, Italy
[3] Univ Siena, Dept Urol Surg, I-53100 Siena, Italy
[4] Univ Siena, Genitourinary Unit, I-53100 Siena, Italy
关键词
castrate resistant; prostate cancer; epirubicin; docetaxel; bone metastases; prostate-specific antigen; MITOXANTRONE PLUS PREDNISONE; TREATMENT-OF-CANCER; BONE METASTASES; CLINICAL-TRIALS; CHEMOTHERAPY; GUIDELINES; SURVIVAL; ANTIGEN; MARKERS;
D O I
10.1038/bjc.2011.5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: This randomised phase II study compared the activity and safety of the combination docetaxel (D)/epirubicin (EPI) with the conventional treatment D/prednisone (P) in advanced castrate-resistant prostate cancer (CRPC) patients. MATERIALS AND METHODS: Patients were randomly assigned to D 30 mgm(-2) as intravenous infusion (i.v.) and EPI 30 mgm(-2) i.v. every week (D/EPI arm), or D 70 mgm(-2) i.v. every 3 weeks and oral P 5 mg twice daily (D/P arm). Chemotherapy was administered until disease progression or unacceptable toxicity. RESULTS: A total of 72 patients were enrolled in the study and randomly assigned to treatment: 37 to D/EPI and 35 to D/P. The median progression-free survival (PFS) was 11.1 months (95% CI 9.2-12.6 months) in the D/EPI arm and 7.7 months (95% CI 5.7-9.4 months) in the D/P arm (P = 0.0002). The median survival was 27.3 months (95% CI 22.1-30.8 months) in the D/EPI arm and 19.8 months (95% CI 14.4-24.8 months) in the D/P arm (P = 0.003). Both regimens were generally well tolerated. CONCLUSION: The treatment of advanced CRPC with weekly D combined with weekly EPI was feasible and tolerable, and led to superior PFS than the treatment with 3-weekly D and oral P. British Journal of Cancer (2011) 104, 613-619. doi:10.1038/bjc.2011.5 www.bjcancer.com Published online 1 February 2011 (C) 2011 Cancer Research UK
引用
收藏
页码:613 / 619
页数:7
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