C Zeng, M A Hernán, L Trevisi, S Sauer, C D Mitnick, C Hewison, M Bastard, P Khan, K J Seung, M L Rich, S Law, M Kikvidze, O Kirakosyan, A Miankou, P Thit, S Mamsa, A Janmohamed, N Melikyan, S Ahmed, D Vargas, A B Binegdie, K Temirova, L Oyewusi, K Philippe, S C Vilbrun, U Khan, H Huerga, M F Franke
{"title":"贝达喹啉、利奈唑胺、氯法齐明“核心”治疗耐多药结核病的有效性。","authors":"C Zeng, M A Hernán, L Trevisi, S Sauer, C D Mitnick, C Hewison, M Bastard, P Khan, K J Seung, M L Rich, S Law, M Kikvidze, O Kirakosyan, A Miankou, P Thit, S Mamsa, A Janmohamed, N Melikyan, S Ahmed, D Vargas, A B Binegdie, K Temirova, L Oyewusi, K Philippe, S C Vilbrun, U Khan, H Huerga, M F Franke","doi":"10.5588/ijtldopen.24.0515","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Treatment outcomes may be compromised among individuals with multidrug/rifampicin-resistant TB (MDR/RR-TB) with fluoroquinolone (FQ) resistance. Among people in whom an FQ was unlikely to be effective, we compared the effectiveness of longer individualised regimens comprised of bedaquiline (Bdq) for 5-8 months, linezolid, and clofazimine to those reinforced with at least 1 Group C drug and/or longer Bdq duration.</p><p><strong>Methods: </strong>We emulated a target trial to compare the effectiveness of initiating and remaining on the core regimen to a regimen reinforced with 1) Bdq for ≥9 months, 2) Bdq for ≥9 months, and delamanid (Dlm), 3) imipenem (Imp), 4) a second-line injectable, or 5) Bdq for ≥9 months, Dlm and Imp. We used cloning, censoring, and inverse-probability weighting to estimate the probabilities of successful treatment.</p><p><strong>Results: </strong>Adjusted probabilities of successful treatment ranged from 0.75 (95% CI 0.61-0.89) to 0.84 (95% CI 0.76-0.91). Ratios of treatment success ranged from 1.01 for regimens reinforced with Bdq ≥9 months (95% CI 0.79-1.28) and Bdq ≥9 months plus Dlm (95% CI 0.81-1.31) to 1.11 for regimens reinforced with an injectable (95% CI 0.92-1.39) and Bdq ≥9 months, Dlm and Imp (95% CI 0.90-1.41).</p><p><strong>Conclusions: </strong>Some reinforced regimens had modestly higher treatment success rates, but estimates were imprecise. Additional studies of strategies for maximising treatment success among individuals with FQ resistance are needed.</p>","PeriodicalId":519984,"journal":{"name":"IJTLD open","volume":"2 5","pages":"269-275"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068452/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effectiveness of a bedaquiline, linezolid, clofazimine 'core' for multidrug-resistant TB.\",\"authors\":\"C Zeng, M A Hernán, L Trevisi, S Sauer, C D Mitnick, C Hewison, M Bastard, P Khan, K J Seung, M L Rich, S Law, M Kikvidze, O Kirakosyan, A Miankou, P Thit, S Mamsa, A Janmohamed, N Melikyan, S Ahmed, D Vargas, A B Binegdie, K Temirova, L Oyewusi, K Philippe, S C Vilbrun, U Khan, H Huerga, M F Franke\",\"doi\":\"10.5588/ijtldopen.24.0515\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Treatment outcomes may be compromised among individuals with multidrug/rifampicin-resistant TB (MDR/RR-TB) with fluoroquinolone (FQ) resistance. Among people in whom an FQ was unlikely to be effective, we compared the effectiveness of longer individualised regimens comprised of bedaquiline (Bdq) for 5-8 months, linezolid, and clofazimine to those reinforced with at least 1 Group C drug and/or longer Bdq duration.</p><p><strong>Methods: </strong>We emulated a target trial to compare the effectiveness of initiating and remaining on the core regimen to a regimen reinforced with 1) Bdq for ≥9 months, 2) Bdq for ≥9 months, and delamanid (Dlm), 3) imipenem (Imp), 4) a second-line injectable, or 5) Bdq for ≥9 months, Dlm and Imp. We used cloning, censoring, and inverse-probability weighting to estimate the probabilities of successful treatment.</p><p><strong>Results: </strong>Adjusted probabilities of successful treatment ranged from 0.75 (95% CI 0.61-0.89) to 0.84 (95% CI 0.76-0.91). Ratios of treatment success ranged from 1.01 for regimens reinforced with Bdq ≥9 months (95% CI 0.79-1.28) and Bdq ≥9 months plus Dlm (95% CI 0.81-1.31) to 1.11 for regimens reinforced with an injectable (95% CI 0.92-1.39) and Bdq ≥9 months, Dlm and Imp (95% CI 0.90-1.41).</p><p><strong>Conclusions: </strong>Some reinforced regimens had modestly higher treatment success rates, but estimates were imprecise. Additional studies of strategies for maximising treatment success among individuals with FQ resistance are needed.</p>\",\"PeriodicalId\":519984,\"journal\":{\"name\":\"IJTLD open\",\"volume\":\"2 5\",\"pages\":\"269-275\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068452/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IJTLD open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5588/ijtldopen.24.0515\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IJTLD open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5588/ijtldopen.24.0515","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:多药/利福平耐药结核病(MDR/RR-TB)伴氟喹诺酮(FQ)耐药患者的治疗结果可能会受到影响。在FQ不太可能有效的人群中,我们比较了由贝达喹啉(Bdq) 5-8个月、利奈唑胺和氯法齐明组成的较长个性化方案与至少1种C组药物和/或较长Bdq持续时间的强化方案的有效性。方法:我们模拟了一项目标试验,比较开始和保持核心方案的有效性与1)Bdq≥9个月,2)Bdq≥9个月,以及delamanid (Dlm), 3)亚胺培南(Imp), 4)二线注射剂,或5)Bdq≥9个月,Dlm和Imp的方案。我们使用克隆,审查和逆概率加权来估计成功治疗的概率。结果:治疗成功的调整概率范围为0.75 (95% CI 0.61-0.89)至0.84 (95% CI 0.76-0.91)。治疗成功率的比值范围从Bdq≥9个月(95% CI 0.79-1.28)和Bdq≥9个月加Dlm (95% CI 0.81-1.31)强化方案的1.01到注射强化方案的1.11 (95% CI 0.92-1.39)和Bdq≥9个月、Dlm和Imp (95% CI 0.90-1.41)。结论:一些强化方案的治疗成功率略高,但估计不准确。需要进一步研究在FQ耐药个体中使治疗成功率最大化的策略。
Effectiveness of a bedaquiline, linezolid, clofazimine 'core' for multidrug-resistant TB.
Background: Treatment outcomes may be compromised among individuals with multidrug/rifampicin-resistant TB (MDR/RR-TB) with fluoroquinolone (FQ) resistance. Among people in whom an FQ was unlikely to be effective, we compared the effectiveness of longer individualised regimens comprised of bedaquiline (Bdq) for 5-8 months, linezolid, and clofazimine to those reinforced with at least 1 Group C drug and/or longer Bdq duration.
Methods: We emulated a target trial to compare the effectiveness of initiating and remaining on the core regimen to a regimen reinforced with 1) Bdq for ≥9 months, 2) Bdq for ≥9 months, and delamanid (Dlm), 3) imipenem (Imp), 4) a second-line injectable, or 5) Bdq for ≥9 months, Dlm and Imp. We used cloning, censoring, and inverse-probability weighting to estimate the probabilities of successful treatment.
Results: Adjusted probabilities of successful treatment ranged from 0.75 (95% CI 0.61-0.89) to 0.84 (95% CI 0.76-0.91). Ratios of treatment success ranged from 1.01 for regimens reinforced with Bdq ≥9 months (95% CI 0.79-1.28) and Bdq ≥9 months plus Dlm (95% CI 0.81-1.31) to 1.11 for regimens reinforced with an injectable (95% CI 0.92-1.39) and Bdq ≥9 months, Dlm and Imp (95% CI 0.90-1.41).
Conclusions: Some reinforced regimens had modestly higher treatment success rates, but estimates were imprecise. Additional studies of strategies for maximising treatment success among individuals with FQ resistance are needed.