Treatment Patterns and Outcomes in Patients With Metastatic Castration-resistant Prostate Cancer in a Real-world Clinical Practice Setting in the United States

恩扎鲁胺 医学 卡巴齐塔塞尔 前列腺癌 多西紫杉醇 强的松 醋酸阿比特龙酯 肿瘤科 内科学 置信区间 阿比曲酮 临床试验 癌症 雄激素剥夺疗法 雄激素受体
作者
Daniel J. George,Oliver Sartor,Kurt Miller,Fred Saad,Bertrand Tombal,Ján Kalinovský,Xiaolong Jiao,Krishna Tangirala,Cora N. Sternberg,Celestia S. Higano
出处
期刊:Clinical Genitourinary Cancer [Elsevier BV]
卷期号:18 (4): 284-294 被引量:142
标识
DOI:10.1016/j.clgc.2019.12.019
摘要

Abstract Background Clinical trials have demonstrated the efficacy of several life-prolonging therapies for metastatic castration-resistant prostate cancer (mCRPC); however, real-world data on their use, survival effect, and safety are limited. Using electronic health record data from the Flatiron Health database, we studied real-world treatment patterns and health outcomes in patients with mCRPC. Patients and Methods We conducted a retrospective, non-interventional cohort analysis of electronic health record data of patients with confirmed mCRPC between January 2013 and September 2017. The primary objective was to describe real-world treatment patterns, including treatment type, duration, and sequencing. Secondary objectives included describing patient characteristics and clinical outcomes. Results Of 2559 patients with mCRPC, 1980 (77%) received at least 1 line of life-prolonging therapy (abiraterone, enzalutamide, docetaxel, cabazitaxel, sipuleucel-T, or radium-223). Of patients receiving first-line therapy, 49% received second-line therapy, and of these, 43% received third-line therapy. Abiraterone/prednisone and enzalutamide accounted for 65% of first-line therapies and 54% of second-line therapies. Docetaxel was the most common third-line therapy (24%). Back-to-back use of abiraterone/prednisone and enzalutamide was common. Radium-223 monotherapy use was 2% in the first-line setting, 3% in the second-line setting, and 8% in the third-line setting. The median overall survival was longer in patients who received life-prolonging therapies (23.7 months; 95% confidence interval: 22.3-25.1 months) than in those who did not (10.1 months; 95% confidence interval: 9.1-11.5 months). Conclusion These real-world insights on over 2500 patients with mCRPC supplement findings from randomized controlled trials and may help to inform clinical trial design, treatment guidelines, and clinical decision-making.
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