Abiraterone acetate plus prednisolone treatment beyond prostate specific antigen and radiographic progression in metastatic castration-resistant prostate cancer patients

被引:4
作者
Biro, Krisztina [1 ]
Budai, Barna [1 ]
Szonyi, Marta [1 ]
Kuronya, Zsofia [1 ]
Gyergyay, Fruzsina [1 ]
Nagyivanyi, Krisztian [1 ]
Geczi, Lajos [1 ]
机构
[1] Natl Inst Oncol, Budapest, Hungary
关键词
Alkaline phosphatase; Clinical progression; Further systemic therapy; Overall survival; Progression-free survival; OPEN-LABEL; CLINICAL-TRIALS; BREAST-CANCER; CHEMOTHERAPY; SURVIVAL; MITOXANTRONE; DOCETAXEL; RECOMMENDATIONS; GUIDELINES; EFFICACY;
D O I
10.1016/j.urolonc.2017.10.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To investigate the overall survival (OS) of chemotherapy refractory patients with metastatic castration-resistant prostate cancer who were treated with abiraterone acetate + prednisolone (AA + P) beyond prostate specific antigen (PSA) and radiographic progression (PRP) until clinical progression in comparison to patients treated until PRP. Methods: At our institute the AA + P treatment started in 2011 in an early-access protocol trial. In October 2012 AA became generally available. From April 2011 to November 2014, 116 patients received AA + P. The clinical trial patients (T; n = 56) were treated beyond PRP until clinical progression. In the nonclinical trial group (NT; n = 57) the treatment was covered until PRP. Three patients are still under treatment. The 2 groups were statistically homogeneous, except AA + P treatment duration. The primary objective was the OS and the secondary the PSA progression-free and radiographic progression-free survivals. Results: The median OS was significantly longer (P<0.0001) in the T group compared to the NT group: 21.9 (95% CI: 16.9-25) vs. 12.5 (9.3-14.1) months, respectively. In univariate analysis there were 11 parameters, which significantly affected OS, but in multivariate Cox analysis only alkaline phosphatase (AP) level at the start of treatment, systemic therapy after AA + P and cohort type (T or NT) proved to independently influence the OS. The progression-free survival curves of T and NT groups did not differ significantly. Conclusions: In our retrospective analysis low levels of AP at the start of treatment, systemic therapy applied after AA + P and treatment beyond PRP proved to be independent factors of longer OS in metastatic castration-resistant prostate cancer. Copyright (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:81.e1 / 81.e7
页数:7
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