Journal
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
Volume 62, Issue 1, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.ijantimicag.2023.106847
Keywords
Efficacy; Hollow fiber system model; M; abscessus; Pharmacokinetics; pharmacodynamics; Safety
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Based on experimental and retrospective clinical studies, it was found that a daily dose of 300 mg of omadacycline achieved good efficacy and had minimal toxicity in the treatment of pulmonary Mab disease. This finding provides a scientific basis for the clinical use of omadacycline.
Background: Guideline-based therapy (GBT) for pulmonary Mycobacterium abscessus (Mab) disease achieves sustained sputum culture conversion (SSCC) rates of 30%; this is reflected by poor efficacy of GBT in the hollow fiber system model of Mab (HFS-Mab), which killed & SIM;1.22 log10 CFU/mL. This study was performed to determine which clinical dose of omadacycline, a tetracycline antibiotic, should be used in combination therapy to treat pulmonary Mab disease for relapse-free cure. Methods: First, omadacycline intrapulmonary concentration-time profiles of seven daily doses were mim-icked in the HFS-Mab model and exposures associated with optimal efficacy were identified. Second, 10,0 0 0 subject Monte-Carlo simulations were performed to determine whether oral omadacycline 300 mg/day achieved these optimal exposures. Third, a retrospective clinical study on omadacycline vs. pri-marily tigecycline-based salvage therapy was conducted to assess rates of SSCC and toxicity. Fourth, a single patient was recruited to validate the findings. Results: Omadacycline efficacy in the HFS-Mab was 2.09 log10 CFU/mL at exposures achieved in > 99% of patients on 300 mg/day omadacycline. In the retrospective study of omadacycline 300 mg/day-based combinations vs. comparators, SSCC was achieved in 8/10 vs. 1/9 (P= 0.006), symptom improvement in 8/8 vs. 5/9 (P= 0.033), toxicity in 0 vs. 9/9 (P < 0.001), and therapy discontinuation due to toxicity in 0 vs. 3/9 (P < 0.001) cases, respectively. In one prospectively recruited patient, omadacycline 300 mg/day salvage therapy achieved SSCC and symptom-resolution in 3 months. Conclusion: Based on the preclinical and clinical data, omadacycline 300 mg/day in combination regimens could be appropriate for testing in Phase III trials in patients with Mab pulmonary disease. & COPY; 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
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