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一步之遥:印度孟买接受贝达喹啉和德拉马尼联合治疗的耐多药结核病患者获得治疗成功。

One Step Forward: Successful End-of-Treatment Outcomes of Patients With Drug-Resistant Tuberculosis Who Received Concomitant Bedaquiline and Delamanid in Mumbai, India.

机构信息

Médecins Sans Frontières, Mumbai, India.

Jupiter Hospital, Thane, Maharashtra, India.

出版信息

Clin Infect Dis. 2021 Nov 2;73(9):e3496-e3504. doi: 10.1093/cid/ciaa1577.

Abstract

BACKGROUND

The Médecins Sans Frontières Clinic in Mumbai, India, has been providing concomitant bedaquiline (BDQ) and delamanid (DLM) in treatment regimen for patients with drug-resistant tuberculosis (DR-TB) and limited therapeutic options, referred from other healthcare institutions, since 2016. The study documents the end-of-treatment outcomes, culture-conversion rates, and serious adverse events (SAEs) during treatment.

METHODS

This was a retrospective cohort study based on routinely collected program data. In clinic, treatment regimens are designed based on culture drug sensitivity test patterns and previous drug exposures, and are provided for 20-22 months. BDQ and DLM are extended beyond 24 weeks as off-label use. Patients who initiated DR-TB treatment including BDQ and DLM (concomitantly for at least 4 weeks) during February 2016-February 2018 were included.

RESULTS

Of the 70 patients included, the median age was 25 (interquartile range [IQR], 22-32) years and 56% were females. All except 1 were fluoroquinolone resistant. The median duration of exposure to BDQ and DLM was 77 (IQR, 43-96) weeks. Thirty-nine episodes of SAEs were reported among 30 (43%) patients, including 5 instances of QTc prolongation, assessed as possibly related to BDQ and/or DLM. The majority (69%) had culture conversion before 24 weeks of treatment. In 61 (87%), use of BDQ and DLM was extended beyond 24 weeks. Successful end-of-treatment outcomes were reported in 49 (70%) patients.

CONCLUSIONS

The successful treatment outcomes of this cohort show that regimens including concomitant BDQ and DLM for longer than 24 weeks are effective and can be safely administered on an ambulatory basis. National TB programs globally should scale up access to life-saving DR-TB regimens with new drugs.

摘要

背景

自 2016 年以来,印度孟买无国界医生组织诊所一直为其他医疗机构转介的耐多药结核病(DR-TB)和治疗选择有限的患者提供贝达喹啉(BDQ)和德拉马尼(DLM)联合治疗方案。本研究记录了治疗结束时的结局、培养转换率和治疗期间的严重不良事件(SAE)。

方法

这是一项基于常规收集的项目数据的回顾性队列研究。在诊所,根据培养药物敏感性试验模式和既往药物暴露情况设计治疗方案,并提供 20-22 个月的治疗。BDQ 和 DLM 作为标签外用药使用超过 24 周。本研究纳入了 2016 年 2 月至 2018 年 2 月期间接受包括 BDQ 和 DLM(至少联合使用 4 周)在内的 DR-TB 治疗的 70 例患者。

结果

70 例患者中,中位年龄为 25 岁(四分位间距[IQR],22-32 岁),56%为女性。除 1 例外,所有患者均对氟喹诺酮类药物耐药。BDQ 和 DLM 的中位暴露时间为 77(IQR,43-96)周。30 例(43%)患者报告了 39 例 SAE,包括 5 例 QTc 延长,评估为可能与 BDQ 和/或 DLM 有关。大多数(69%)患者在治疗的 24 周前培养转为阳性。61 例(87%)患者的 BDQ 和 DLM 使用时间超过 24 周。49 例(70%)患者的治疗结束时结局成功。

结论

该队列的成功治疗结果表明,使用贝达喹啉和德拉马尼联合治疗方案超过 24 周是有效的,并且可以安全地进行门诊治疗。全球各国的国家结核病规划应扩大获得新药物的救命性耐多药结核病治疗方案的机会。

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