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PMID: 12241657 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, U.S. Gov't, P.H.S.

Rifapentine and isoniazid once a week versus rifampicin and isoniazid twice a week for treatment of drug-susceptible pulmonary tuberculosis in HIV-negative patients: a randomised clinical trial.

Lancet (London, England) ·Vol. 360 ·No. 9332 ·2002-08-17 ·Pages 528-34

Benator D, Bhattacharya M, Bozeman L, Burman W, Cantazaro A, Chaisson R, Gordin F, Horsburgh CR, Horton J, Khan A, Lahart C, Metchock B, Pachucki C, Stanton L, Vernon A, Villarino ME, Wang YC, Weiner M, Weis S, Tuberculosis Trials Consortium

Abstract

Rifapentine has a long half-life in serum, which suggests a possible treatment once a week for tuberculosis. We aimed to compare rifapentine and isoniazid once a week with rifampicin and isoniazid twice a week. We did a randomised, multicentre, open-label trial in the USA and Canada of HIV-negative people with drug-susceptible pulmonary tuberculosis who had completed 2 months of a 6-month treatment regimen. We randomly allocated patients directly observed treatment with either 600 mg rifapentine plus 900 mg isoniazid once a week or 600 mg rifampicin plus 900 mg isoniazid twice a week. Primary outcome was failure/relapse. Analysis was by intention to treat. 1004 patients were enrolled (502 per treatment group). 928 successfully completed treatment, and 803 completed the 2-year 4-month study. Crude rates of failure/relapse were 46/502 (9.2%) in those on rifapentine once a week, and 28/502 (5.6%) in those given rifampicin twice a week (relative risk 1.64, 95% CI 1.04-2.58, p=0.04). By proportional hazards regression, five characteristics were independently associated with increased risk of failure/relapse: sputum culture positive at 2 months (hazard ratio 2.8, 95% CI 1.7-4.6); cavitation on chest radiography (3.0, 1.6-5.9); being underweight (3.0, 1.8-4.9); bilateral pulmonary involvement (1.8, 1.0-3.1); and being a non-Hispanic white person (1.8, 1.1-3.0). Adjustment for imbalances in 2-month culture and cavitation diminished the association of treatment group with outcome (1.34; 0.83-2.18; p=0.23). Of participants without cavitation, rates of failure/relapse were 6/210 (2.9%) in the once a week group and 6/241 (2.5%) in the twice a week group (relative risk 1.15; 95% CI 0.38-3.50; p=0.81). Rates of adverse events and death were similar in the two treatment groups. Rifapentine once a week is safe and effective for treatment of pulmonary tuberculosis in HIV-negative people without cavitation on chest radiography. Clinical, radiographic, and microbiological data help to identify patients with tuberculosis who are at increased risk of failure or relapse when treated with either regimen.

MeSH Terms
Antibiotics, Antitubercular/administration & dosage Drug Administration Schedule Drug Therapy, Combination Ethnicity Female Humans Isoniazid/administration & dosage Male Middle Aged Radiography, Thoracic Rifampin/administration & dosage,analogs & derivatives Sputum/microbiology Treatment Outcome Tuberculosis, Pulmonary/diagnostic imaging,drug therapy,microbiology
Chemicals
Antibiotics, Antitubercular Isoniazid Rifampin rifapentine
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Benator Debra
Bhattacharya Mondira
Bozeman Lorna
Burman William
Cantazaro Antonino
Chaisson Richard
Gordin Fred
Horsburgh C Robert
Horton James
Khan Awal
Lahart Christopher
Metchock Beverly
Pachucki Constance
Stanton Llewellyn
Vernon Andrew
Villarino M Elsa
Wang Yong Chen
Weiner Marc
Weis Stephen
Tuberculosis Trials Consortium
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
Published
2002-08-17
Pages
528-34
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Grants
NCRR NIH HHS · M01-RR00827 · United States
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