Saluzzo Francesca, Adepoju Victor Abiola, Duarte Raquel, Lange Christoph, Phillips Patrick P J
Vita-Salute San Raffaele University, Milan, Italy.
Contributed equally as first authors.
Breathe (Sheff). 2023 Sep;19(3):230028. doi: 10.1183/20734735.0028-2023. Epub 2023 Oct 10.
In the past 2 years, remarkable advances have been made in shortening tuberculosis (TB) treatment. In particular, four clinical trials (Study 31/A5349, Nix-TB, ZeNix and TB-PRACTECAL) have provided evidence of the efficacy of regimens based on new and repurposed drugs: the 4-month regimen for drug-susceptible TB, and the 6-month bedaquiline-pretomanid-linezolid regimen with or without moxifloxacin for multidrug-resistant/rifampicin-resistant TB. Even if the evidence at the basis of these new regimens is compelling, several questions remain open, particularly concerning linezolid dose finding, the upsurging threat of bedaquiline-resistant and the feasibility of applying these results to the paediatric population. Several ongoing trials may fill the remaining gaps and produce further reliable evidence to address the outstanding questions in TB treatment shortening.
在过去两年中,结核病治疗疗程的缩短取得了显著进展。特别是四项临床试验(研究31/A5349、Nix-TB、ZeNix和TB-PRACTECAL)提供了基于新药物和重新利用药物的治疗方案有效性的证据:针对药物敏感型结核病的4个月疗程,以及针对耐多药/利福平耐药结核病的含或不含莫西沙星的6个月贝达喹啉-普瑞马尼德-利奈唑胺疗程。即使这些新治疗方案所依据的证据很有说服力,但仍有几个问题悬而未决,特别是关于利奈唑胺剂量确定、贝达喹啉耐药性激增的威胁以及将这些结果应用于儿科人群的可行性。正在进行的几项试验可能会填补剩余的空白,并产生进一步可靠的证据来解决结核病治疗疗程缩短方面的未决问题。