Zeng Chengbo, Hernán Miguel A, Trevisi Letizia, Sauer Sara, Mitnick Carole D, Hewison Catherine, Bastard Mathieu, Khan Palwasha, Seung Kwonjune J, Rich Michael L, Law Stephanie, Kikvidze Marina, Kirakosyan Ohanna, Miankou Alexey, Thit Phone, Mamsa Shahid, Janmohamed Aleeza, Melikyan Nara, Ahmed Saman, Vargas Dante, Binegdie Amsalu Bekele, Temirova Kulbaram, Oyewusi Lawrence, Philippe Kerline, Vilbrun Stalz C, Khan Uzma, Huerga Helena, Franke Molly F
medRxiv. 2024 Jan 19:2024.01.18.24301453. doi: 10.1101/2024.01.18.24301453.
Treatment outcomes may be compromised among patients with multidrug- or rifampicin-resistant tuberculosis with additional fluoroquinolone resistance. Evidence is needed to inform optimal treatment for these patients.
We compared the effectiveness of longer individualized regimens comprised of bedaquiline for 5 to 8 months, linezolid, and clofazimine to those reinforced with at least 1 third-tier drug and/or longer duration of bedaquiline.
We emulated a target trial to compare the effectiveness of initiating and remaining on the core regimen to one of five regimens reinforced with (1) bedaquiline for ≥9 months, (2) bedaquiline for ≥9 months and delamanid, (3) imipenem, (4) a second-line injectable, or (5) delamanid and imipenem. We included patients in whom a fluoroquinolone was unlikely to be effective based on drug susceptibility testing and/or prior exposure. Our analysis consisted of cloning, censoring, and inverse-probability weighting to estimate the probability of successful treatment.
Adjusted probabilities of successful treatment were high across regimens, ranging from 0.75 (95%CI:0.61, 0.89) to 0.84 (95%CI:0.76, 0.91). We found no substantial evidence that any of the reinforced regimens improved effectiveness of the core regimen, with ratios of treatment success ranging from 1.01 for regimens reinforced with bedaquiline ≥9 months (95%CI:0.79, 1.28) and bedaquiline ≥9 months plus delamanid (95%CI:0.81, 1.31) to 1.11 for regimens reinforced by a second-line injectable (95%CI:0.92, 1.39) and delamanid and imipenem (95%CI:0.90, 1.41).
High treatment success underscores the effectiveness of regimens comprised of bedaquiline, linezolid, and clofazimine, highlighting the need for expanded access to these drugs.
耐多药或耐利福平的结核病患者若同时对氟喹诺酮类药物耐药,其治疗效果可能会受到影响。需要证据来指导针对这些患者的最佳治疗方案。
我们比较了由5至8个月的贝达喹啉、利奈唑胺和氯法齐明组成的较长个体化治疗方案与至少加用1种三线药物和/或延长贝达喹啉使用时间的强化治疗方案的有效性。
我们模拟了一项目标试验,比较开始并持续使用核心治疗方案与以下五种强化治疗方案之一的有效性:(1)贝达喹啉使用≥9个月;(2)贝达喹啉使用≥9个月并加用德拉马尼;(3)亚胺培南;(4)二线注射剂;(5)德拉马尼和亚胺培南。我们纳入了根据药敏试验和/或既往用药史判断氟喹诺酮类药物可能无效的患者。我们的分析包括克隆、删失和逆概率加权,以估计治疗成功的概率。
各治疗方案调整后的治疗成功概率均较高,范围为0.75(95%置信区间:0.61, 0.89)至0.84(95%置信区间:0.76, 0.91)。我们没有发现充分证据表明任何一种强化治疗方案能提高核心治疗方案的有效性,治疗成功比例范围为:使用贝达喹啉≥9个月的强化方案为1.01(95%置信区间:0.79, 1.28),使用贝达喹啉≥9个月加用德拉马尼的强化方案为1.01(95%置信区间:0.81, 1.31),使用二线注射剂强化的方案为1.11(95%置信区间:0.92, 1.39),使用德拉马尼和亚胺培南强化的方案为1.11(95%置信区间:0.90, 1.41)。
高治疗成功率强调了由贝达喹啉、利奈唑胺和氯法齐明组成的治疗方案的有效性,突出了扩大这些药物可及性的必要性。