Predictors of relapse or maintenance of response in pediatric and adult patients with attention-deficit/hyperactivity disorder following discontinuation of long-term treatment with atomoxetine.

Johannes Thome, Ralf W Dittmann, Laurence L Greenhill, Sarah Lipsius, Yoko Tanaka, Chris Bushe, Rodrigo Escobar, Alexandra N Heinloth, Himanshu Upadhyaya
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引用次数: 1

Abstract

We identified relapse/maintenance-of-response (MOR) predictors following discontinuation of long-term atomoxetine treatment in pediatric and adult patients with attention-deficit/hyperactivity disorder (ADHD) and assessed correlations between ADHD symptoms and quality of life (QoL). Post hoc analyses of data from two randomized, double-blind, placebo-controlled, phase 3 withdrawal studies in patients with ADHD meeting predefined response criteria before randomization. Study 1: patients (N = 163; 6-15 years) received atomoxetine (1.2-1.8 mg/kg/day) for 1 year, followed by randomization to atomoxetine (n = 81) or placebo (n = 82) for 6 months. Study 2: patients (N = 524; 18-50 years) received atomoxetine (80-100 mg/day) for ~6 months, followed by randomization to atomoxetine (n = 266) or placebo (n = 258) for ~6 months. Placebo patients were used for the analyses. Relapse: ≥50% worsening of prerandomization improvement in ADHD symptoms and ≥2 level severity increase on the Clinical Global Impression-Severity (CGI-S) scale at 2 consecutive visits; MOR: retaining ≥75% of prerandomization symptom improvement and CGI-S ≤ 2 at all visits (study 1); retaining ≥70% of prerandomization symptom improvement and CGI-S ≤ 3 at all visits (study 2). In adults, statistically significantly (P ≤ .05) increased likelihood of relapse was associated with prerandomization presence of Conners' Adult Attention-Deficit/Hyperactivity Disorder Rating Scale-Investigator-Rated:Screening Version (CAARS-Inv:SV) items "difficulty awaiting turn" and "careless mistakes." In pediatric patients, less MOR was associated with prerandomization presence of ADHD Rating Scale-IV-Parent Version Investigator-Rated item "does not listen"; in adults, less MOR was associated with prerandomization presence of CAARS-Inv:SV items "loses things" and "difficulty awaiting turn." Changes in patients' QoL after withdrawal from atomoxetine moderately correlated with changes in ADHD symptoms in pediatric patients and mildly in adults.

停止长期阿托西汀治疗后儿童和成人注意缺陷/多动障碍患者复发或维持反应的预测因素
我们确定了儿童和成人注意缺陷/多动障碍(ADHD)患者停止长期阿托西汀治疗后的复发/反应维持(MOR)预测因素,并评估了ADHD症状与生活质量(QoL)之间的相关性。对两项随机、双盲、安慰剂对照、3期停药研究的数据进行事后分析,这些研究的ADHD患者在随机化之前符合预定义的反应标准。研究1:患者(N = 163;6-15岁)接受托莫西汀(1.2-1.8 mg/kg/天)治疗1年,随后随机分配到托莫西汀(n = 81)或安慰剂(n = 82)治疗6个月。研究2:患者(N = 524;18-50岁)接受托莫西汀(80- 100mg /天)治疗约6个月,随后随机分配到托莫西汀(n = 266)或安慰剂(n = 258)治疗约6个月。安慰剂患者被用于分析。复发:随机化前ADHD症状改善恶化≥50%,连续2次就诊时临床总体印象严重程度(CGI-S)量表加重≥2级;MOR:随机化前症状改善率≥75%,且每次就诊时CGI-S≤2(研究1);在所有就诊中,保持≥70%的随机化前症状改善和CGI-S≤3(研究2)。在成人中,统计学上显著(P≤0.05)复发的可能性增加与随机化前Conners'成人注意力缺陷/多动障碍评定量表-调查员评定:筛选版(CAARS-Inv:SV)项目“等待轮到困难”和“粗心错误”的存在相关。在儿科患者中,较少的more与随机前ADHD评定量表iv -家长版调查员评定项目“不听”的存在相关;在成人中,较少的MOR与随机化前CAARS-Inv:SV项目的存在“丢失东西”和“等待轮到的困难”有关。停用托莫西汀后患者生活质量的变化与儿童患者ADHD症状的变化有中度相关性,与成人患者有轻度相关性。
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