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Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa
BACKGROUND: Delafloxacin (DLX) is a broad-spectrum fluoroquinolone antibiotic under FDA review for the treatment of ABSSSI. Previous studies determined DLX bacterial stasis and 1-log(10) bacterial reduction free AUC(0-24) / MIC (fAUC(0-24)/MIC) targets for Escherichia coli (EC) and Pseudomonas aerug...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631342/ http://dx.doi.org/10.1093/ofid/ofx163.1228 |
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author | Hoover, Randall Marra, Andrea Duffy, Erin Cammarata, Sue K |
author_facet | Hoover, Randall Marra, Andrea Duffy, Erin Cammarata, Sue K |
author_sort | Hoover, Randall |
collection | PubMed |
description | BACKGROUND: Delafloxacin (DLX) is a broad-spectrum fluoroquinolone antibiotic under FDA review for the treatment of ABSSSI. Previous studies determined DLX bacterial stasis and 1-log(10) bacterial reduction free AUC(0-24) / MIC (fAUC(0-24)/MIC) targets for Escherichia coli (EC) and Pseudomonas aeruginosa (PA) in a mouse thigh infection model. The resulting PK/PD targets were used to predict DLX target attainment probabilities (TAP) in humans. METHODS: Monte Carlo simulations were used to estimate TAP with DLX 300 mg IV, q12hr. Human DLX plasma pharmacokinetics were determined in patients with ABSSSI in a Phase 3 clinical trial. Individual AUC values were analyzed and determined to be log-normally distributed. The parameters of the AUC distribution were used to simulate random values for fAUC(24), which then were combined with random MIC values based on 2014–2015 US distributions of skin and soft tissue isolates of EC (n = 108) and PA (n = 40), to calculate PK/PD TAPs. RESULTS: DLX fAUC(0-24)/MIC targets for bacterial stasis and 1-log(10) bacterial reduction for EC were 14.5 and 26.2, and for PA were 3.81 and 5.02, respectively. The Monte Carlo simulations for EC predicted TAPs of 98.7% for stasis at an MIC of 0.25 μg/mL, and 99.3% for 1-log(10) bacterial reduction at an MIC of 0.12 μg/mL. The simulations for PA predicted TAPs of 97.3% for stasis and 86.5% for 1-log(10) bacterial reduction at an MIC of 1 μg/mL. CONCLUSION: DLX 300 mg IV, q12hr, should achieve fAUC24/MIC ratios that are adequate to treat ABSSSI caused by most contemporary isolates of EC and PA. For EC, isolates with DLX MICs ≤0.25 μg/mL comprised 73% of all isolates. For PA, isolates with DLX MICs ≤1 μg/mL comprised 88% of all isolates. Similar results would be expected for TAP with oral DLX 450 mg, q12hr. DISCLOSURES: R. Hoover, Melinta Therapeutics: Consultant, Consulting fee; A. Marra, Melinta Therapeutics: Employee, Salary; E. Duffy, Melinta Therapeutics: Employee, Salary; S. K. Cammarata, Melinta Therapeutics: Employee, Salary |
format | Online Article Text |
id | pubmed-5631342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56313422017-11-07 Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa Hoover, Randall Marra, Andrea Duffy, Erin Cammarata, Sue K Open Forum Infect Dis Abstracts BACKGROUND: Delafloxacin (DLX) is a broad-spectrum fluoroquinolone antibiotic under FDA review for the treatment of ABSSSI. Previous studies determined DLX bacterial stasis and 1-log(10) bacterial reduction free AUC(0-24) / MIC (fAUC(0-24)/MIC) targets for Escherichia coli (EC) and Pseudomonas aeruginosa (PA) in a mouse thigh infection model. The resulting PK/PD targets were used to predict DLX target attainment probabilities (TAP) in humans. METHODS: Monte Carlo simulations were used to estimate TAP with DLX 300 mg IV, q12hr. Human DLX plasma pharmacokinetics were determined in patients with ABSSSI in a Phase 3 clinical trial. Individual AUC values were analyzed and determined to be log-normally distributed. The parameters of the AUC distribution were used to simulate random values for fAUC(24), which then were combined with random MIC values based on 2014–2015 US distributions of skin and soft tissue isolates of EC (n = 108) and PA (n = 40), to calculate PK/PD TAPs. RESULTS: DLX fAUC(0-24)/MIC targets for bacterial stasis and 1-log(10) bacterial reduction for EC were 14.5 and 26.2, and for PA were 3.81 and 5.02, respectively. The Monte Carlo simulations for EC predicted TAPs of 98.7% for stasis at an MIC of 0.25 μg/mL, and 99.3% for 1-log(10) bacterial reduction at an MIC of 0.12 μg/mL. The simulations for PA predicted TAPs of 97.3% for stasis and 86.5% for 1-log(10) bacterial reduction at an MIC of 1 μg/mL. CONCLUSION: DLX 300 mg IV, q12hr, should achieve fAUC24/MIC ratios that are adequate to treat ABSSSI caused by most contemporary isolates of EC and PA. For EC, isolates with DLX MICs ≤0.25 μg/mL comprised 73% of all isolates. For PA, isolates with DLX MICs ≤1 μg/mL comprised 88% of all isolates. Similar results would be expected for TAP with oral DLX 450 mg, q12hr. DISCLOSURES: R. Hoover, Melinta Therapeutics: Consultant, Consulting fee; A. Marra, Melinta Therapeutics: Employee, Salary; E. Duffy, Melinta Therapeutics: Employee, Salary; S. K. Cammarata, Melinta Therapeutics: Employee, Salary Oxford University Press 2017-10-04 /pmc/articles/PMC5631342/ http://dx.doi.org/10.1093/ofid/ofx163.1228 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Hoover, Randall Marra, Andrea Duffy, Erin Cammarata, Sue K Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title | Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title_full | Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title_fullStr | Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title_full_unstemmed | Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title_short | Human Target Attainment Probabilities for Delafloxacin against Escherichia coli and Pseudomonas aeruginosa |
title_sort | human target attainment probabilities for delafloxacin against escherichia coli and pseudomonas aeruginosa |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631342/ http://dx.doi.org/10.1093/ofid/ofx163.1228 |
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