| Literature DB >> 30361241 |
Lei Gao1,2,2, Haoran Zhang1,2, Henan Xin1,2, Jianmin Liu3,2, Shouguo Pan4,2, Xiangwei Li1, Ling Guan3, Fei Shen3, Zisen Liu4, Dakuan Wang4, Xueling Guan3, Jiaoxia Yan4, Hengjing Li1, Boxuan Feng1, Xuefang Cao1, Yu Chen3, Wei Cui3, Zongde Zhang5, Yu Ma5, Xiaoyou Chen5, Xinhua Zhou5, Qi Jin1,2.
Abstract
Latent tuberculosis infection (LTBI) management is now a critical component of the World Health Organization's End TB Strategy.In this randomised controlled trial (Chinese Clinical Trial Registry identifier ChiCTR-IOR-15007202), two short-course regimens with rifapentine plus isoniazid (a 3-month once-weekly regimen and a 2-month twice-weekly regimen) were initially designed to be evaluated for rural residents aged 50-69 years with LTBI in China.Due to the increasingly rapid growth and unexpected high frequency of adverse effects, the treatments were terminated early (after 8 weeks for the once-weekly regimen and after 6 weeks for the twice-weekly regimen). In the modified intention-to-treat analysis on the completed doses, the cumulative rate of active disease during 2 years of follow-up was 1.21% (14 out of 1155) in the untreated controls, 0.78% (10 out of 1284) in the group that received the 8-week once-weekly regimen and 0.46% (six out of 1299) in the group that received the 6-week twice-weekly regimen. The risk of active disease was decreased, with an adjusted hazard ratio of 0.63 (95% CI 0.27-1.43) and 0.41 (95% CI 0.15-1.09) for the treatments, respectively. No significant difference was found in the occurrence of hepatotoxicity (1.02% (13 out of 1279) versus 1.17% (15 out of 1279); p=0.704).The short regimens tested must be used with caution among the elderly because of the high rates of adverse effects. Further work is necessary to test the ultrashort regimens in younger people with LTBI.Entities:
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Year: 2018 PMID: 30361241 DOI: 10.1183/13993003.01470-2018
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671