Duration of pretomanid/moxifloxacin/pyrazinamide therapy compared with standard therapy based on time-to-extinction mathematics.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 02 2020
Historique:
received: 28 07 2019
revised: 29 09 2019
accepted: 08 10 2019
pubmed: 13 11 2019
medline: 10 6 2021
entrez: 13 11 2019
Statut: ppublish

Résumé

Animal models have suggested that the combination of pretomanid with pyrazinamide and moxifloxacin (PaMZ) may shorten TB therapy duration to 3-4 months. Here, we tested that in the hollow-fibre system model of TB (HFS-TB). A series of HFS-TB experiments were performed to compare the kill rates of the PaMZ regimen with the standard three-drug combination therapy. HFS-TB experiments were performed with bacilli in log-phase growth treated for 28 days, intracellular bacilli treated daily for 28 days and semi-dormant Mycobacterium tuberculosis treated with daily therapy for 56 days for sterilizing effect. Next, time-to-extinction equations were employed, followed by morphism transformation and Latin hypercube sampling, to determine the proportion of patients who achieved a time to extinction of 3, 4 or 6 months with each regimen. Using linear regression, the HFS-TB sterilizing effect rates of the PaMZ regimen versus the standard-therapy regimen during the 56 days were 0.18 (95% credible interval=0.13-0.23) versus 0.15 (95% credible interval=0.08-0.21) log10 cfu/mL/day, compared with 0.16 (95% credible interval=0.13-0.18) versus 0.11 (95% credible interval=0.09-0.13) log10 cfu/mL/day in the Phase II clinical trial, respectively. Using time-to-extinction and Latin hypercube sampling modelling, the expected percentages of patients in which the PaMZ regimen would achieve sterilization were 40.37% (95% credible interval=39.1-41.34) and 72.30% (95% credible interval=71.41-73.17) at 3 and 4 months duration of therapy, respectively, versus 93.67% (95% credible interval=93.18-94.13) at 6 months for standard therapy. The kill rates of the PaMZ regimen were predicted to be insufficient to achieve cure in less than 6 months in most patients.

Identifiants

pubmed: 31713607
pii: 5622906
doi: 10.1093/jac/dkz460
pmc: PMC6966096
doi:

Substances chimiques

Antitubercular Agents 0
Nitroimidazoles 0
pretomanid 0
Pyrazinamide 2KNI5N06TI
Moxifloxacin U188XYD42P

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

392-399

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy.

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Auteurs

Shashikant Srivastava (S)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.

Devyani Deshpande (D)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.

Gesham Magombedze (G)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.

Johanna van Zyl (J)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.

Kayle Cirrincione (K)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.

Katherine Martin (K)

Praedicare Laboratories, Dallas, TX, USA.

Paula Bendet (P)

Praedicare Laboratories, Dallas, TX, USA.

Alexander Berg (A)

Critical Path to TB Drug Regimens, Critical Path Institute, Tucson, AZ, USA.

Debra Hanna (D)

Critical Path to TB Drug Regimens, Critical Path Institute, Tucson, AZ, USA.
Bill & Melinda Gates Foundation, Seattle, WA, USA.

Klaus Romero (K)

Critical Path to TB Drug Regimens, Critical Path Institute, Tucson, AZ, USA.

Dave Hermann (D)

Bill & Melinda Gates Foundation, Seattle, WA, USA.

Tawanda Gumbo (T)

Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.
Praedicare Laboratories, Dallas, TX, USA.
Lung Infection and Immunity Unit, Division of Pulmonology and UCT Lung Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa.

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Classifications MeSH