What Predicts Minimal Response to Abiraterone in Metastatic Castrate-resistant Prostate Cancer?

被引:0
|
作者
Davies, Rhian Sian [1 ]
Smith, Christian [1 ]
Button, Michael Robert [1 ]
Tanguay, Jacob [1 ]
Barber, Jim [1 ]
Palaniappan, Nachiappan [1 ]
Staffurth, John [1 ,2 ]
Lester, Jason Francis [1 ]
机构
[1] Velindre Canc Ctr, Cardiff, S Glam, Wales
[2] Cardiff Univ, Inst Canc Genet, Cardiff CF10 3AX, S Glam, Wales
关键词
Metastatic; castrate-resistant; prostate cancer; abiraterone; predictors response; drug sequencing; ANDROGEN DEPRIVATION THERAPY; MITOXANTRONE PLUS PREDNISONE; INCREASED SURVIVAL; RECEPTOR; BICALUTAMIDE; ACETATE; ENZALUTAMIDE; INHIBITOR; ANTAGONISM; MECHANISMS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Several treatments have been shown to prolong survival in metastatic castrate-resistant prostate cancer (mCRPC); the optimum sequencing of these is not established. We investigated methods of identifying patients with mCRPC unlikely to respond to abiraterone. Patients and Methods: A retrospective analysis was carried-out in 47 consecutive patients with mCRPC treated sequentially with androgen deprivation (LHRH alpha), bicalutamide, docetaxel then abiraterone. Results: The median progression-free survival in patients treated with abiraterone was shorter in those with <= 18 months' response to LHRH alpha (118 vs. 279 days; p=0.018), bicalutamide non-responders (91 vs. 196 days; p=0.003) and patients with <= 6 months' response to docetaxel (102 vs. 294 days; p<0.001). The median overall survival was also shorter (348 vs. 815 days, p=0.016; 413 vs. 752 days, p=0.009; and 325 vs. 727 days, p<0.04, respectively). Conclusion: A response of <= 18 months' to LHRH alpha, non-response to bicalutamide and <= 6 months' response to docetaxel predicted poor response to abiraterone.
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页码:5615 / 5621
页数:7
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