Cargando…

Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam

Background: The World health organization (WHO) recently recommended standardized all-oral shorter regimens for rifampicin resistant Tuberculosis (RR-TB). For highly resistant Tuberculosis patients such as pre-XDR-TB: RR-TB plus additional resistance to fluoroquinolones (FQ), the 6–9-months bedaquil...

Descripción completa

Detalles Bibliográficos
Autores principales: Nguyen, Thi Mai Phuong, Nguyen, Binh Hoa, Hoang, Thi Thanh Thuy, Nguyen, Hoang Anh, Vu, Dinh Hoa, Nguyen, Mai Hoa, Nguyen, Bao Ngoc, Decroo, Tom, Nguyen, Viet Nhung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614239/
https://www.ncbi.nlm.nih.gov/pubmed/36313324
http://dx.doi.org/10.3389/fphar.2022.1023704
_version_ 1784820153382338560
author Nguyen, Thi Mai Phuong
Nguyen, Binh Hoa
Hoang, Thi Thanh Thuy
Nguyen, Hoang Anh
Vu, Dinh Hoa
Nguyen, Mai Hoa
Nguyen, Bao Ngoc
Decroo, Tom
Nguyen, Viet Nhung
author_facet Nguyen, Thi Mai Phuong
Nguyen, Binh Hoa
Hoang, Thi Thanh Thuy
Nguyen, Hoang Anh
Vu, Dinh Hoa
Nguyen, Mai Hoa
Nguyen, Bao Ngoc
Decroo, Tom
Nguyen, Viet Nhung
author_sort Nguyen, Thi Mai Phuong
collection PubMed
description Background: The World health organization (WHO) recently recommended standardized all-oral shorter regimens for rifampicin resistant Tuberculosis (RR-TB). For highly resistant Tuberculosis patients such as pre-XDR-TB: RR-TB plus additional resistance to fluoroquinolones (FQ), the 6–9-months bedaquiline (bedaquiline)-based regimens or BDQ-based long regimens are recommended. The role of second-line injectable (SLI) drugs in the treatment of drug resistant TB is restricted because of safety concerns. Nevertheless, it is not well-known how all-oral long regimens (BDQ-long) perform compared to SLI-containing long regimens (BDQ/SLI-long) in terms of safety and effectiveness among patients with highly resistant TB. Method: A prospective observational cohort of patients with RR-TB additionally resistant to fluoroquinolones and/or second-line injectable, treated with either BDQ-long or BDQ/SLI-long regimens according to the guidance of the National Tuberculosis Program of Vietnam, enrolled between December 2015 and June 2017. Results: Of 99 patients enrolled, 42 (42%) patients were treated with BDQ-long and 57 (57%) with BDQ/SLI-long. More than 85% of patients were previously exposed to both FQ and SLI. FQ and SLI resistance were confirmed in 28 (67%) and 41 (98%) in the BDQ-long cohort and 48 (84%) and 17 (30%) in the BDQ/SLI-long cohort, respectively. Treatment success was achieved among 29 (69%) and 46 (81%) patients on the BDQ-long and BDQ/SLI-long regimen, respectively (p = 0.2). For both regimens, median time to first smear/culture sputum conversion was 2 months. All patients experienced at least one adverse event (AE) and 85% of them had at least one severe Adverse events. The median time to a first severe adverse event was 2 months. Among patients treated with BDQ-long a higher proportion of patients had three QT-prolonging drugs in the regimen (26.2% versus 7.0%; p = 0.009). The severe prolonged QTcF was observed in 22 (52.4%) and 22 (38.6%) patients on BDQ-long and BDQ/SLI-long, respectively. Overall, 30 (30%) patients had to either temporary or permanently discontinued or more TB drugs due to AEs. Conclusion: Treatment success was similar for both all-oral and SLI-containing BDQ-based long regimens in highly resistant TB patients. Both regimens had a similar high frequency of AEs. For both BDQ-long and BDQ/SLI-long regimens active AEs monitoring is essential.
format Online
Article
Text
id pubmed-9614239
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-96142392022-10-29 Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam Nguyen, Thi Mai Phuong Nguyen, Binh Hoa Hoang, Thi Thanh Thuy Nguyen, Hoang Anh Vu, Dinh Hoa Nguyen, Mai Hoa Nguyen, Bao Ngoc Decroo, Tom Nguyen, Viet Nhung Front Pharmacol Pharmacology Background: The World health organization (WHO) recently recommended standardized all-oral shorter regimens for rifampicin resistant Tuberculosis (RR-TB). For highly resistant Tuberculosis patients such as pre-XDR-TB: RR-TB plus additional resistance to fluoroquinolones (FQ), the 6–9-months bedaquiline (bedaquiline)-based regimens or BDQ-based long regimens are recommended. The role of second-line injectable (SLI) drugs in the treatment of drug resistant TB is restricted because of safety concerns. Nevertheless, it is not well-known how all-oral long regimens (BDQ-long) perform compared to SLI-containing long regimens (BDQ/SLI-long) in terms of safety and effectiveness among patients with highly resistant TB. Method: A prospective observational cohort of patients with RR-TB additionally resistant to fluoroquinolones and/or second-line injectable, treated with either BDQ-long or BDQ/SLI-long regimens according to the guidance of the National Tuberculosis Program of Vietnam, enrolled between December 2015 and June 2017. Results: Of 99 patients enrolled, 42 (42%) patients were treated with BDQ-long and 57 (57%) with BDQ/SLI-long. More than 85% of patients were previously exposed to both FQ and SLI. FQ and SLI resistance were confirmed in 28 (67%) and 41 (98%) in the BDQ-long cohort and 48 (84%) and 17 (30%) in the BDQ/SLI-long cohort, respectively. Treatment success was achieved among 29 (69%) and 46 (81%) patients on the BDQ-long and BDQ/SLI-long regimen, respectively (p = 0.2). For both regimens, median time to first smear/culture sputum conversion was 2 months. All patients experienced at least one adverse event (AE) and 85% of them had at least one severe Adverse events. The median time to a first severe adverse event was 2 months. Among patients treated with BDQ-long a higher proportion of patients had three QT-prolonging drugs in the regimen (26.2% versus 7.0%; p = 0.009). The severe prolonged QTcF was observed in 22 (52.4%) and 22 (38.6%) patients on BDQ-long and BDQ/SLI-long, respectively. Overall, 30 (30%) patients had to either temporary or permanently discontinued or more TB drugs due to AEs. Conclusion: Treatment success was similar for both all-oral and SLI-containing BDQ-based long regimens in highly resistant TB patients. Both regimens had a similar high frequency of AEs. For both BDQ-long and BDQ/SLI-long regimens active AEs monitoring is essential. Frontiers Media S.A. 2022-10-14 /pmc/articles/PMC9614239/ /pubmed/36313324 http://dx.doi.org/10.3389/fphar.2022.1023704 Text en Copyright © 2022 Nguyen, Nguyen, Hoang, Nguyen, Vu, Nguyen, Nguyen, Decroo and Nguyen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Nguyen, Thi Mai Phuong
Nguyen, Binh Hoa
Hoang, Thi Thanh Thuy
Nguyen, Hoang Anh
Vu, Dinh Hoa
Nguyen, Mai Hoa
Nguyen, Bao Ngoc
Decroo, Tom
Nguyen, Viet Nhung
Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title_full Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title_fullStr Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title_full_unstemmed Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title_short Safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-XDR tuberculosis in Vietnam
title_sort safety and effectiveness of all-oral and injectable-containing, bedaquiline-based long treatment regimen for pre-xdr tuberculosis in vietnam
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614239/
https://www.ncbi.nlm.nih.gov/pubmed/36313324
http://dx.doi.org/10.3389/fphar.2022.1023704
work_keys_str_mv AT nguyenthimaiphuong safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT nguyenbinhhoa safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT hoangthithanhthuy safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT nguyenhoanganh safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT vudinhhoa safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT nguyenmaihoa safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT nguyenbaongoc safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT decrootom safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam
AT nguyenvietnhung safetyandeffectivenessofalloralandinjectablecontainingbedaquilinebasedlongtreatmentregimenforprexdrtuberculosisinvietnam