Stroup T Scott
Department of Psychiatry, University of North Carolina at Chapel Hill, 10301 Neuroscience Hospital, Chapel Hill, North Carolina 27599-7160, USA.
Am J Med. 2007 Apr;120(4 Suppl 1):S26-31. doi: 10.1016/j.amjmed.2007.02.005.
The treatment of mental illness presents an opportunity to examine the heterogeneity of treatment effects. The Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) schizophrenia trial was sponsored by the National Institute of Mental Health (NIMH) to evaluate the effectiveness of antipsychotic medications for schizophrenia in broad patient populations and in scenarios representative of standard clinical practice. Trial inclusion criteria were broad and exclusion criteria were minimal, allowing for a heterogeneous study population. The majority of patients in each phase 1 treatment group discontinued their randomly assigned treatment owing to inadequate efficacy, intolerable side effects, or other reasons. Phase 2 of CATIE featured 2 treatment pathways (efficacy and tolerability) with randomized follow-up medication based on the reason for discontinuation of the previous antipsychotic drug. Outcome differences between treatment groups and variable responses to medications across the study suggest why multiple medication trials are common and may be necessary in the treatment of schizophrenia. Collectively, the CATIE results highlight variable response in the treatment of schizophrenia and demonstrate the need for individualized therapy based on variations in drug efficacy and tolerability among patients.
精神疾病的治疗为研究治疗效果的异质性提供了契机。美国国立精神卫生研究所(NIMH)发起了精神分裂症干预有效性临床抗精神病药物试验(CATIE),以评估抗精神病药物在广泛患者群体以及标准临床实践场景中治疗精神分裂症的有效性。试验纳入标准宽泛,排除标准极少,从而形成了一个异质性的研究群体。每个1期治疗组中的大多数患者因疗效不佳、无法耐受的副作用或其他原因而中断了随机分配的治疗。CATIE的2期有2条治疗途径(疗效和耐受性),根据前一种抗精神病药物停药的原因进行随机后续用药。治疗组之间的结果差异以及整个研究中对药物的可变反应表明了为什么在精神分裂症治疗中多次药物试验很常见且可能是必要的。总体而言,CATIE的结果突出了精神分裂症治疗中的可变反应,并表明需要根据患者之间药物疗效和耐受性的差异进行个体化治疗。