High-Dose Isoniazid Lacks EARLY Bactericidal Activity against Isoniazid-resistant Tuberculosis Mediated by katG Mutations: A Randomized Phase II Clinical Trial.
Kamunkhwala GausiElisa H IgnatiusVeronique De JagerCaryn UptonSoyeon KimAshley McKhannLaura MoranLubbe WiesnerFlorian von Groote-BidlingmaierPhilip MarzinekNaadira VankerJoseph YvetotSamuel PierreSusan L RosenkranzSusan SwindellsAndreas H DiaconEric L NuermbergerPaolo DentiKelly E DooleyPublished in: American journal of respiratory and critical care medicine (2024)
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).
Keyphrases
- mycobacterium tuberculosis
- phase ii
- high dose
- open label
- clinical trial
- phase iii
- pulmonary tuberculosis
- double blind
- low dose
- wild type
- stem cell transplantation
- placebo controlled
- multidrug resistant
- emergency department
- physical activity
- squamous cell carcinoma
- mass spectrometry
- electronic health record
- drug induced
- hepatitis c virus
- deep learning
- machine learning
- human immunodeficiency virus
- klebsiella pneumoniae