This paper presents a protocol, or design, for the analysis of a comparative effectiveness evaluation of abiraterone acetate against enzalutamide, two drugs given to prostate cancer patients. The design explicitly make use of differences in prescription practices across 21 Swedish county councils for the estimation of the two drugs comparative effectiveness on overall mortality, pain and skeleton related events. The design requires that the county factor: (1) affects the probability to be treated (i.e. being prescribed abiraterone acetate instead of enzalutamide) but (2) is not otherwise correlated with the outcome. The fist assumption is validated in the data. The latter assumption may be untenable and also not possible to formally test. However, the validity of this assumption is evaluated in a sensitivity analysis, where data on the two morbidity outcomes (i.e. pain and skeleton related events) observed before prescription date are used. We find that the county factor does \emph{not} explain these two pre-measured outcomes. The implication is that we cannot reject the validity of the design.
翻译:本文提出一个协议或设计,用于分析对抗抗丙氨酸乙酮乙酸乙酯的两种给前列腺癌病人的药物的比较有效性评估,设计明确利用21个瑞典县议会在处方做法上的差异来估计两种药物的总体死亡率、疼痛和骨骼相关事件的相对有效性。设计要求县因子:(1) 影响治疗的概率(即被处方乙酮乙酸乙酸乙酯,而不是酶甲酸乙酯),(2) 与结果无关,但(2) 与结果无关。拳头假设在数据中得到验证。后一种假设可能站不住脚,也不可能正式测试。然而,在敏感度分析中评估了这一假设的有效性,其中使用了在处方日期之前观察到的两种发病率结果(即疼痛和骨骼相关事件)的数据。我们发现,县因子确实解释了这两个预先测定的结果。这意味着我们不能否定设计的有效性。