Ke Hui, Gui Xuwei, Sun Wenwen, Zhang Shaojun, Yang Yan, Zhang Zhemin, Fan Lin
Department of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai Clinic and Research Center of Tuberculosis, Shanghai Key Laboratory of Tuberculosis, Shanghai, People's Republic of China.
Infect Drug Resist. 2023 Aug 7;16:5055-5064. doi: 10.2147/IDR.S419996. eCollection 2023.
To evaluate the safety, tolerability, and efficacy of prolonged bedaquiline (Bdq) treatment in patients with multi-drug/rifampin-resistant tuberculosis (MDR/RR-TB).
This prospective cohort study was performed from August 2018 to August 2021. Patients diagnosed with MDR/RR-TB who met the inclusion criteria were prospectively included. Patients were treated with individual regimens of 18-20 months containing Bdq for six months or a prolonged course of nine or 12 months according to treatment demands, and the efficacy and safety with a different course of Bdq-containing regimens were compared and evaluated.
A total of 159 MDR/RR-TB patients were included in the study, including 96 cases with six months of Bdq, 50 cases with nine months of Bdq, and 13 patients with 12 months of Bdq. The treatment success rates were 89.6%, 90%, and 84.6% in Bdq at six months, nine months, and 12 months, respectively, which were not statistically different (P = 0.85). The main adverse events (AEs) were anemia, thrombocytopenia, and liver dysfunction in all patients, with no significant difference among the three groups. Patients who had fewer drugs chosen, disseminated lesions or lesions that were slowly absorbed, and severe cavities were the common reasons for prolonged use of Bdq.
Prolonged course use of Bdq from six months to 12 months clinically proved to be safe and efficient, and patients with severe or disseminated lesions had the chance to prolong the use of Bdq for more than six months to achieve optimal treatment outcomes.
评估延长使用贝达喹啉(Bdq)治疗耐多药/利福平耐药结核病(MDR/RR-TB)患者的安全性、耐受性和疗效。
本前瞻性队列研究于2018年8月至2021年8月进行。前瞻性纳入符合纳入标准的MDR/RR-TB确诊患者。根据治疗需求,患者接受为期18 - 20个月的个体化治疗方案,其中Bdq使用6个月,或根据治疗需求延长疗程至9个月或12个月,并比较和评估含不同疗程Bdq方案的疗效和安全性。
共纳入159例MDR/RR-TB患者,其中6个月Bdq治疗的有96例,9个月Bdq治疗的有50例,12个月Bdq治疗的有13例。Bdq治疗6个月、9个月和12个月的治疗成功率分别为89.6%、90%和84.6%,差异无统计学意义(P = 0.85)。所有患者的主要不良事件为贫血、血小板减少和肝功能障碍,三组间无显著差异。药物选择较少、有播散性病变或病变吸收缓慢以及有严重空洞的患者是延长使用Bdq的常见原因。
临床证明,将Bdq疗程从6个月延长至12个月是安全有效的,有严重或播散性病变的患者有机会延长Bdq使用时间超过6个月以实现最佳治疗效果。