Davis Sonia M, Stroup T Scott, Koch Gary G, Davis Clarence E, Rosenheck Robert A, Lieberman Jeffrey A
Quintiles, Inc.
Columbia University Department of Psychiatry.
Stat Biopharm Res. 2011;3(2):253-265. doi: 10.1198/sbr.2011.10013. Epub 2012 Jan 1.
Time until all-cause treatment discontinuation was the primary outcome of the CATIE trial. We discuss the advantages and disadvantages of this outcome, and evaluate its association with clinical correlates through graphical response profiles. We investigate the characteristics of patients who discontinued for patient decision, including a reclassification of patient decision into other reasons. All-cause discontinuation is compared to a related outcome, time until treatment failure. Patients who discontinued had lower quality of life scores than other patients. Patients discontinuing for lack of efficacy had worsened efficacy scores compared with an improvement for other patients. Those who discontinued for patient decision had lower compliance. Blinded reclassification of discontinuation for patient decision identified 5% of cases as lack of efficacy and 21% as intolerable side effects. Reclassified patients participated in the next study phase at a higher rate than those remaining as patient decision (67% vs. 10%). Treatment group differences for time to discontinuation due to patient decision were attenuated after censoring the reclassified patients, but were still suggestive. Treatment comparisons for time to treatment failure were consistent with all cause discontinuation, although somewhat smaller. All-cause discontinuation is recommended as a simple and comprehensive outcome for pharmaceutical Phase II-IV clinical trials.
全因治疗中断时间是CATIE试验的主要结局。我们讨论了这一结局的优缺点,并通过图形化反应曲线评估其与临床相关因素的关联。我们调查了因患者决定而中断治疗的患者特征,包括将患者决定重新分类为其他原因。将全因中断与一个相关结局——治疗失败时间进行比较。中断治疗的患者生活质量得分低于其他患者。因疗效不佳而中断治疗的患者,其疗效得分恶化,而其他患者则有所改善。因患者决定而中断治疗的患者依从性较低。对因患者决定而中断治疗进行盲法重新分类后发现,5%的病例为疗效不佳,21%为无法耐受的副作用。重新分类的患者进入下一研究阶段的比例高于仍归类为患者决定的患者(67%对10%)。在剔除重新分类的患者后,因患者决定导致的治疗中断时间的治疗组差异有所减弱,但仍具有提示性。治疗失败时间的治疗比较与全因中断一致,尽管幅度略小。全因中断被推荐作为药物II-IV期临床试验的一个简单而全面的结局。