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High-Dose Isoniazid Lacks EARLY Bactericidal Activity against Isoniazid-resistant Tuberculosis Mediated by katG Mutations: A Randomized Phase II Clinical Trial.
Gausi, Kamunkhwala; Ignatius, Elisa H; De Jager, Veronique; Upton, Caryn; Kim, Soyeon; McKhann, Ashley; Moran, Laura; Wiesner, Lubbe; von Groote-Bidlingmaier, Florian; Marzinek, Philip; Vanker, Naadira; Yvetot, Joseph; Pierre, Samuel; Rosenkranz, Susan L; Swindells, Susan; Diacon, Andreas H; Nuermberger, Eric L; Denti, Paolo; Dooley, Kelly E.
Afiliação
  • Gausi K; Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
  • Ignatius EH; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • De Jager V; TASK, Cape Town, South Africa.
  • Upton C; TASK, Cape Town, South Africa.
  • Kim S; Frontier Science Foundation, Brookline, Massachusetts.
  • McKhann A; Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
  • Moran L; Social & Scientific Systems, a DLH Company, Silver Spring, Maryland.
  • Wiesner L; Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
  • von Groote-Bidlingmaier F; TASK, Cape Town, South Africa.
  • Marzinek P; Frontier Science Foundation, Amherst, New York.
  • Vanker N; Social & Scientific Systems, a DLH Company, Silver Spring, Maryland.
  • Yvetot J; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska; and.
  • Pierre S; GHESKIO Centers, Port-au-Prince, Haiti.
  • Rosenkranz SL; Frontier Science Foundation, Brookline, Massachusetts.
  • Swindells S; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska; and.
  • Diacon AH; Social & Scientific Systems, a DLH Company, Silver Spring, Maryland.
  • Nuermberger EL; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Denti P; Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
  • Dooley KE; Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, Tennessee.
Am J Respir Crit Care Med ; 210(3): 343-351, 2024 08 01.
Article em En | MEDLINE | ID: mdl-38564365
ABSTRACT
Rationale Observational studies suggest that high-dose isoniazid may be efficacious in treating multidrug-resistant tuberculosis. However, its activity against Mycobacterium tuberculosis (M.tb) with katG mutations (which typically confer high-level resistance) is not established.

Objectives:

To characterize the early bactericidal activity (EBA) of high-dose isoniazid in patients with tuberculosis caused by katG-mutated M.tb.

Methods:

A5312 was a phase IIA randomized, open-label trial. Participants with tuberculosis caused by katG-mutated M.tb were randomized to receive 15 or 20 mg/kg isoniazid daily for 7 days. Daily sputum samples were collected for quantitative culture. Intensive pharmacokinetic sampling was performed on Day 6. Data were pooled across all A5312 participants for analysis (drug-sensitive, inhA-mutated, and katG-mutated M.tb). EBA was determined using nonlinear mixed-effects modeling. Measurements and Main

Results:

Of 80 treated participants, 21 had katG-mutated M.tb. Isoniazid pharmacokinetics were best described by a two-compartment model with an effect of NAT2 acetylator phenotype on clearance. Model-derived maximum concentration and area under the concentration-time curve in the 15 and 20 mg/kg groups were 15.0 and 22.1 mg/L and 57.6 and 76.8 mg ⋅ h/L, respectively. Isoniazid bacterial kill was described using an effect compartment and a sigmoidal maximum efficacy relationship. Isoniazid potency against katG-mutated M.tb was approximately 10-fold lower than in inhA-mutated M.tb. The highest dose of 20 mg/kg did not demonstrate measurable EBA, except against a subset of slow NAT2 acetylators (who experienced the highest concentrations). There were no grade 3 or higher drug-related adverse events.

Conclusions:

This study found negligible bactericidal activity of high-dose isoniazid (15-20 mg/kg) in the majority of participants with tuberculosis caused by katG-mutated M.tb. Clinical trial registered with www.clinicaltrials.gov (NCT01936831).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Tuberculose Resistente a Múltiplos Medicamentos / Isoniazida / Mutação / Mycobacterium tuberculosis / Antituberculosos Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: África do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Tuberculose Resistente a Múltiplos Medicamentos / Isoniazida / Mutação / Mycobacterium tuberculosis / Antituberculosos Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: África do Sul