Division of Experimental Oncology/Unit of Urology URI, IRCCS Ospedale San Raffaele, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.
PLoS One. 2020 Dec 28;15(12):e0244462. doi: 10.1371/journal.pone.0244462. eCollection 2020.
The aim of this study was to assess time on treatment with abiraterone and enzalutamide, two androgen receptor targeted (ART) drugs, the impact on time on treatment of time interval without drug supply between prescription fillings, and adherence to treatment.
By use of data from The National Prostate Cancer Register, The Prescribed Drug Registry and the Patient Registry, time on treatment with the abiraterone and enzalutamide was analyzed in all men with castration resistant prostate cancer (CRPC) in Sweden 2015-2019. Three time intervals between consecutive fillings, i.e. time without drug supply, were assessed. Adherence to the treatment was evaluated by use of the Medication Possession Ratio. Kaplan Meier analysis and multivariable Cox regression model were used to assess factors affecting time on treatment.
Between January 2015 and October 2019, 1803 men filled a prescription for abiraterone and 4 534 men filled a prescription for enzalutamide. With a time interval of 30 days or less between two fillings, median time on treatment was 4.9 months (IQR 2.6-11.7) for abiraterone and 8.0 months (IQR 3.6-16.4) for enzalutamide. In sensitivity analyses, allowing for no more than 14 days without drug supply between fillings, median time on treatment was 3.9 months (IQR 2.1-9.0) for abiraterone and 5.9 months (IQR 2.8-12.1) for enzalutamide. Allowing for any time period without drug between fillings, median time on treatment was 5.7 months (IQR 2.7-14.0) for abiraterone and 9.8 months (IQR 4.4-21.0) for enzalutamide. Adherence to treatment was above 90% for both drugs.
Time on treatment with abiraterone and enzalutamide was shorter in clinical practice than in randomized controlled trials and varied almost two-fold with time interval without drug. Adherence to treatment was high. The main limitation of our study was the lack of data on use of chemotherapy.
本研究旨在评估接受雄激素受体靶向(ART)药物阿比特龙和恩扎卢胺治疗的时间、两次处方配药之间无药物供应的时间间隔对治疗时间的影响,以及治疗的依从性。
利用来自全国前列腺癌登记处、处方药品登记处和患者登记处的数据,分析了 2015 年至 2019 年瑞典所有接受去势抵抗性前列腺癌(CRPC)治疗的男性使用阿比特龙和恩扎卢胺的治疗时间。评估了连续两次配药之间的三个时间间隔,即无药物供应的时间。通过药物使用量比例评估治疗的依从性。采用 Kaplan-Meier 分析和多变量 Cox 回归模型评估影响治疗时间的因素。
2015 年 1 月至 2019 年 10 月,1803 名男性开了阿比特龙处方,4534 名男性开了恩扎卢胺处方。两次配药之间的时间间隔为 30 天或更短,阿比特龙的中位治疗时间为 4.9 个月(IQR 2.6-11.7),恩扎卢胺的中位治疗时间为 8.0 个月(IQR 3.6-16.4)。在敏感性分析中,允许两次配药之间最多有 14 天无药物供应,阿比特龙的中位治疗时间为 3.9 个月(IQR 2.1-9.0),恩扎卢胺的中位治疗时间为 5.9 个月(IQR 2.8-12.1)。允许两次配药之间任意时间无药物供应,阿比特龙的中位治疗时间为 5.7 个月(IQR 2.7-14.0),恩扎卢胺的中位治疗时间为 9.8 个月(IQR 4.4-21.0)。两种药物的治疗依从性均在 90%以上。
阿比特龙和恩扎卢胺的治疗时间在临床实践中比随机对照试验短,且随无药物供应时间间隔的变化几乎翻了一番。治疗的依从性很高。本研究的主要局限性是缺乏化疗使用数据。