Safety of Abiraterone Acetate in Castration-resistant Prostate Cancer Patients With Concomitant Cardiovascular Risk Factors

被引:25
|
作者
Procopio, Giuseppe [1 ]
Grassi, Paolo [1 ]
Testa, Isabella [1 ]
Verzoni, Elena [1 ]
Torri, Valter [4 ]
Salvioni, Roberto [2 ]
Valdagni, Riccardo [3 ]
de Braud, Filippo [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Dept Med Oncol, I-20133 Milan, Italy
[2] Fdn IRCCS Ist Nazl Tumori, Dept Urol, I-20133 Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Prostate Programme, I-20133 Milan, Italy
[4] Mario Negri Inst Pharmacol Res, Milan, Italy
关键词
abiraterone acetate; castration-resistant prostate cancer; cardiovascular comorbidities; safety; INCREASED SURVIVAL; PLUS PREDNISONE; DOCETAXEL; THERAPY; INHIBITOR; CYP17; CHEMOTHERAPY; MITOXANTRONE; TRIAL;
D O I
10.1097/COC.0b013e3182a790ce
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives:The aim of this study was to evaluate the safety profile of abiraterone acetate (AA) in metastatic castration-resistant prostate cancer (mCRPC) men with cardiovascular comorbidity, as little conclusive safety data are available in this patient subset.Patients and Methods:A retrospective analysis of mCRPC patients with controlled cardiovascular comorbidities, receiving AA 1000 mg administered orally once daily and prednisone 5 mg twice daily, between April 2011 and July 2012, was performed. All clinical and instrumental variables and toxicity data were analyzed by descriptive statistics: mean, standard deviation, minimum and maximum values for continuous variables, and absolute and relative frequencies for categorical variables.Results:A total of 51 mCRPC patients were evaluated. Metastatic sites included the bone (74%), lungs, and liver (26%). All patients were previously treated with at least 2 lines of hormone and 1 docetaxel-based chemotherapy. Preexisting cardiac risk factors included hypertension (41%), cardiac ischemia (12%), arrhythmias (6%), dislipidemia (18%), and hyperglycemia (30%). No grade 3-4 adverse events were observed. Grade 1-2 adverse events included fluid retention (18%), asthenia (15%), and hypertension (16%). Median progression-free survival was 5.1 months (95% confidence interval, 0.5-12). Prostate specific antigen assessment revealed a good overall disease control rate (64%).Conclusions:AA appears to be safe and well tolerated even in patients with cardiovascular comorbidities or with increased risk factors for cardiovascular diseases.
引用
收藏
页码:479 / 482
页数:4
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