A Randomised Phase II Trial Comparing Docetaxel Plus Prednisone with Docetaxel Plus Prednisone Plus Low-Dose Cyclophosphamide in Castration-Resistant Prostate Cancer

被引:9
作者
Porsch, Markus [1 ]
Ulrich, Matthias [3 ]
Wendler, Johann Jakob [1 ]
Liehr, Uwe-Bernd [1 ]
Reiher, Frank [4 ]
Janitzky, Andreas [1 ]
Baumunk, Daniel [1 ]
Schindele, Daniel [1 ]
Seseke, Florian [5 ]
Lux, Anke [2 ]
Schostak, Martin [1 ]
机构
[1] Univ Magdeburg, Fak Med, Klin Urol & Kinderurol, DE-39120 Magdeburg, Germany
[2] Univ Magdeburg, Fak Med, Inst Biometrie & Med Informat, DE-39120 Magdeburg, Germany
[3] AMEOS Klinikum St Salvator, Klin Urol & Kinderurol, Halberstadt, Germany
[4] AMEOS Klinikum, Klin Urol Kinderurol & Uroonkol, Haldensleben, Germany
[5] Krankenhaus Martha Maria, Urol Klin, Halle, Germany
关键词
Docetaxel; Prednisone; Cyclophosphamide; Prostate cancer; Castration-resistant prostate cancer; CHEMOTHERAPY; TAXOTERE; DEXAMETHASONE; ESTRAMUSTINE; MITOXANTRONE; MANAGEMENT; CARCINOMA; THERAPY;
D O I
10.1159/000369781
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Docetaxel plus prednisone is a standard treatment for castration-resistant prostate cancer. Cyclophosphamide may be an effective combination partner. Methods: This randomised, multicentre, phase II trial compared the combination therapy of docetaxel plus prednisone plus cyclophosphamide with the standard therapy of docetaxel plus prednisone. Results: Thirty-three patients received six 3-week treatment cycles (in total 171 cycles). During treatment, an adequate decline in prostate-specific antigen was seen in both groups (p = 0.068) without between-group differences (p = 0.683). No relevant differences between within-group changes were observed for blood pressure, weight, pain score, laboratory variables or quality of life. There were no serious side effects apart from leucopenia requiring treatment (docetaxel + prednisone + cyclophosphamide arm) and no drug-related withdrawals; all three fatalities were considered to be cancer related. Conclusions: The oncological effectiveness and tolerability of docetaxel plus prednisone were supported; an additional effect of cyclophosphamide was not detected. However, the small number of patients and short observation period restrict the generalisability of the results. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:129 / 134
页数:6
相关论文
共 25 条
[1]  
[Anonymous], 2014, CYCL FACH
[2]  
[Anonymous], 2013, GES BUND ZENTR KREBS, P16
[3]   Weekly high-dose calcitriol and docetaxel in metastatic androgen-independent prostate cancer [J].
Beer, TM ;
Eilers, KM ;
Garzotto, M ;
Egorin, MJ ;
Lowe, BA ;
Henner, WD .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :123-128
[4]   Phase II trial of single-agent weekly docetaxel in hormone-refractory, symptomatic, metastatic carcinoma of the prostate [J].
Berry, W ;
Dakhil, S ;
Gregurich, MA ;
Asmar, L .
SEMINARS IN ONCOLOGY, 2001, 28 (04) :8-15
[5]   Phase II trial of cyclophosphamide, vincristine, and dexamethasone in the treatment of androgen-independent prostate carcinoma [J].
Daliani, DD ;
Assikis, V ;
Tu, SM ;
Papandreou, CN ;
Pagliaro, LC ;
Holtkamp, T ;
Wang, XM ;
Thall, PF ;
Logothetis, CJ .
CANCER, 2003, 97 (03) :561-567
[6]   ASSEMBLY OF PURIFIED GDP TUBULIN INTO MICROTUBULES INDUCED BY TAXOL AND TAXOTERE - REVERSIBILITY, LIGAND STOICHIOMETRY, AND COMPETITION [J].
DIAZ, JF ;
ANDREU, JM .
BIOCHEMISTRY, 1993, 32 (11) :2747-2755
[7]  
Eisenberger M A, 1988, Semin Urol, V6, P303
[8]   Potential for improvement of docetaxel-based chemotherapy: a pharmacological review [J].
Engels, FK ;
Sparreboom, A ;
Mathot, RAA ;
Verweij, J .
BRITISH JOURNAL OF CANCER, 2005, 93 (02) :173-177
[9]   Addition of estramustine to chemotherapy and survival of patients with castration-refractory prostate cancer: a meta-analysis of individual patient data [J].
Fizazi, Karim ;
Le Maitre, Aurelie ;
Hudes, Gary ;
Berry, William R. ;
Kelly, W. Kevin ;
Eymord, Jean-Christophe ;
Logothetis, Christopher J. ;
Pignon, Jean-Pierre ;
Michiels, Stefan .
LANCET ONCOLOGY, 2007, 8 (11) :994-1000
[10]  
Friedland D, 1999, SEMIN ONCOL, V26, P19