4.6 Article

Emergence of bedaquiline resistance in a high tuberculosis burden country

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EUROPEAN RESPIRATORY JOURNAL
卷 59, 期 3, 页码 -

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EUROPEAN RESPIRATORY SOC JOURNALS LTD
DOI: 10.1183/13993003.00621-2021

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资金

  1. CARE consortium (Common Action against HIV/TB/HCV across the Regions of Europe)
  2. European Union's Horizon 2020 Research and Innovation programme [825673]
  3. German Excellence Cluster Precision Medicine in Chronic Inflammation [EXC 2167]
  4. German Center for Infection Research
  5. H2020 Societal Challenges Programme [825673] Funding Source: H2020 Societal Challenges Programme

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This study analyzed pre-existing and emerging bedaquiline resistance in the treatment of multidrug-resistant tuberculosis (MDR-TB), as well as risk factors associated with treatment failure and death. The findings showed that bedaquiline-based MDR-TB treatment requires a functional background regimen to achieve high cure rates and prevent the evolution of bedaquiline resistance.
Rationale Bedaquiline has been classified as a group A drug for the treatment of multidrug-resistant tuberculosis (MDR-TB) by the World Health Organization; however, globally emerging resistance threatens the effectivity of novel MDR-TB treatment regimens. Objectives We analysed pre-existing and emerging bedaquiline resistance in bedaquiline-based MDR-TB therapies, and risk factors associated with treatment failure and death. Methods In a cross-sectional cohort study, we employed patient data, whole-genome sequencing (WGS) and phenotyping of Mycobacterium tuberculosis complex (MTBC) isolates. We could retrieve baseline isolates from 30.5% (62 out of 203) of all MDR-TB patients who received bedaquiline between 2016 and 2018 in the Republic of Moldova. This includes 26 patients for whom we could also retrieve a follow-up isolate. Measurements and main results At baseline, all MTBC isolates were susceptible to bedaquiline. Among 26 patients with available baseline and follow-up isolates, four (15.3%) patients harboured strains which acquired bedaquiline resistance under therapy, while one (3.8%) patient was re-infected with a second bedaquiline-resistant strain. Treatment failure and death were associated with cavitary disease (p=0.011), and any additional drug prescribed in the bedaquiline-containing regimen with WGS-predicted resistance at baseline (OR 1.92 per unit increase, 95% CI 1.15-3.21; p=0.012). Conclusions MDR-TB treatments based on bedaquiline require a functional background regimen to achieve high cure rates and to prevent the evolution of bedaquiline resistance. Novel MDR-TB therapies with bedaquiline require timely and comprehensive drug resistance monitoring.

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