创伤治疗的突破:与帕罗西汀和舍曲林相比,MDMA 辅助心理疗法的安全性和有效性。

Focus (American Psychiatric Publishing) Pub Date : 2023-07-01 Epub Date: 2023-06-28 DOI:10.1176/appi.focus.23021013
Allison A Feduccia, Lisa Jerome, Berra Yazar-Klosinski, Amy Emerson, Michael C Mithoefer, Rick Doblin
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引用次数: 0

摘要

治疗不成功的创伤后应激障碍(PTSD)是一种严重且危及生命的疾病。盐酸帕罗西汀和盐酸舍曲林这两种药物已被美国食品和药物管理局(FDA)批准用于治疗创伤后应激障碍。对创伤后应激障碍药物疗法的分析发现,与安慰剂相比,药物疗法仅有轻微至中等程度的效果。多学科迷幻研究协会(MAPS)从美国食品和药物管理局(FDA)获得了突破性疗法认定(BTD),认定3,4-亚甲二氧基甲基苯丙胺(MDMA)辅助心理疗法治疗创伤后应激障碍,依据是汇总分析显示这种疗法具有较大的疗效。本综述涵盖支持 BTD 的数据。在这种治疗方法中,MDMA 与心理治疗同时进行,每月最多三次,每次 8 小时。参加者事先为这些疗程做好准备,并在后续的综合心理治疗疗程中处理疗程中产生的材料。通过比较帕罗西汀和舍曲林的审批数据以及第二阶段研究的汇总数据,MAPS 表明,与现有的药物疗法相比,MDMA 辅助心理疗法在安全性和疗效方面都有很大改进。与舍曲林和帕罗西汀试验相比,MDMA辅助心理疗法研究的辍学率较低。由于亚甲二氧基甲基苯丙胺只在有限的疗程中在直接观察下施用,因此几乎不会出现转移用途、意外或故意过量或停药后出现戒断症状的情况。BTD资格加快了MAPS 3期试验在全球范围内的发展,并计划于2021年提交申请,以获得美国食品和药物管理局的批准。最初发表于《Front Psychiatry 2019; 10:650》。
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Breakthrough for Trauma Treatment: Safety and Efficacy of MDMA-Assisted Psychotherapy Compared to Paroxetine and Sertraline.

Unsuccessfully treated posttraumatic stress disorder (PTSD) is a serious and life-threatening disorder. Two medications, paroxetine hydrochloride and sertraline hydrochloride, are approved treatments for PTSD by the Food and Drug Administration (FDA). Analyses of pharmacotherapies for PTSD found only small to moderate effects when compared with placebo. The Multidisciplinary Association for Psychedelic Studies (MAPS) obtained Breakthrough Therapy Designation (BTD) from the FDA for 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for treatment of PTSD on the basis of pooled analyses showing a large effect size for this treatment. This review covers data supporting BTD. In this treatment, MDMA is administered with psychotherapy in up to three monthly 8-h sessions. Participants are prepared for these sessions beforehand, and process material arising from the sessions in follow-up integrative psychotherapy sessions. Comparing data used for the approval of paroxetine and sertraline and pooled data from Phase 2 studies, MAPS demonstrated that MDMA-assisted psychotherapy constitutes a substantial improvement over available pharmacotherapies in terms of safety and efficacy. Studies of MDMA-assisted psychotherapy had lower dropout rates compared to sertraline and paroxetine trials. As MDMA is only administered under direct observation during a limited number of sessions, there is little chance of diversion, accidental or intentional overdose, or withdrawal symptoms upon discontinuation. BTD status has expedited the development of MAPS phase 3 trials occurring worldwide, leading up to a planned submission seeking FDA approval in 2021. Appeared originally in Front Psychiatry 2019; 10:650.

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