Tecovirimat Use under Expanded Access to Treat Mpox in the United States, 2022-2023.

NEJM evidence Pub Date : 2024-10-01 Epub Date: 2024-09-13 DOI:10.1056/EVIDoa2400189
Patricia A Yu, Riad Elmor, Kalimah Muhammad, Yon C Yu, Agam K Rao
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Abstract

Background: During the ongoing outbreak of clade II monkeypox virus (MPXV), many U.S. patients were prescribed tecovirimat, an antiviral drug that was made available under an expanded access Investigational New Drug (EA-IND) program. We evaluated EA-IND data to summarize characteristics of treated patients, outcomes, and serious adverse events (SAEs).

Methods: We evaluated data from patients prescribed tecovirimat from May 29, 2022, through July 10, 2023. Baseline patient characteristics, clinical courses, and outcomes were evaluated via intake forms, outcome forms, and patient diaries. Data were summarized in aggregate by human immunodeficiency virus (HIV) status and by comorbidities of special interest. Reported SAEs were also compiled.

Results: Tecovirimat was prescribed for over 7100 patients in the United States, most often for lesions in sensitive anatomical areas, such as certain anogenital lesions (83.5%; 5135 out of 6148 patients), and pain (52.5%; 3227 out of 6148 patients). The demographic and clinical characteristics mirrored those of patients worldwide. Among the 7181 patients with returned intake forms, 1626 also had returned outcome forms (22.6%). Many patients with severe immunocompromise (e.g., HIV with CD4 counts <200 cells/μl) received multiple courses of tecovirimat (43.1%; 22 out of 51 patients), including intravenously, and often experienced poor outcomes (35.3%; 18 out of 51 patients). Overall, 223 SAEs and 40 deaths were reported. Most SAEs were among patients who were severely immunocompromised, one of whom experienced hallucinations after tecovirimat was administered at twice the standard dose.

Conclusions: Tecovirimat was used extensively. The returned EA-IND data suggest that life-threatening or protracted infections occurred in persons who were severely immunocompromised. SAEs were not commonly reported. The EA-IND data are not definitive; controlled clinical trial data are essential to elucidating if and how tecovirimat should be used.

2022-2023 年美国使用 Tecovirimat 治疗麻风病的扩大准入情况。
背景:在二代猴痘病毒(MPXV)疫情持续爆发期间,许多美国患者获得了特考韦瑞(tecovirimat)抗病毒药物处方。我们评估了 EA-IND 数据,总结了接受治疗的患者特征、治疗结果和严重不良事件(SAEs):我们评估了 2022 年 5 月 29 日至 2023 年 7 月 10 日期间处方替考韦瑞的患者数据。我们通过入组表、结果表和患者日记对患者的基线特征、临床过程和结果进行了评估。数据按人体免疫缺陷病毒(HIV)状态和特别关注的合并症汇总。此外,还对报告的 SAE 进行了汇总:在美国,7100 多名患者使用了特考韦瑞马,最常见的原因是敏感解剖部位的病变,如某些肛门病变(83.5%;6148 名患者中有 5135 名)和疼痛(52.5%;6148 名患者中有 3227 名)。这些患者的人口统计学特征和临床特征与世界各地的患者相同。在 7181 名交回接收表的患者中,1626 名也交回了结果表(22.6%)。许多免疫力严重低下的患者(如 CD4 细胞计数达标的艾滋病病毒感染者)都使用了替考韦瑞(Tecovirimat):特考韦瑞被广泛使用。返回的 EA-IND 数据表明,严重免疫力低下的患者会发生危及生命或持续时间较长的感染。报告的 SAE 并不常见。EA-IND 数据并不是决定性的;对照临床试验数据对于阐明是否以及如何使用替考韦瑞至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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