Investigational Antifungal Agents for Invasive Mycoses: A Clinical Perspective.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
31 08 2022
Historique:
received: 27 10 2021
pubmed: 6 1 2022
medline: 3 9 2022
entrez: 5 1 2022
Statut: ppublish

Résumé

Treatment of invasive fungal infections (IFIs) remains challenging, because of the limitations of the current antifungal agents (ie, mode of administration, toxicity, and drug-drug interactions) and the emergence of resistant fungal pathogens. Therefore, there is an urgent need to expand our antifungal armamentarium. Several compounds are reaching the stage of phase II or III clinical assessment. These include new drugs within the existing antifungal classes or displaying similar mechanism of activity with improved pharmacologic properties (rezafungin and ibrexafungerp) or first-in-class drugs with novel mechanisms of action (olorofim and fosmanogepix). Although critical information regarding the performance of these agents in heavily immunosuppressed patients is pending, they may provide useful additions to current therapies in some clinical scenarios, including IFIs caused by azole-resistant Aspergillus or multiresistant fungal pathogens (eg, Candida auris, Lomentospora prolificans). However, their limited activity against Mucorales and some other opportunistic molds (eg, some Fusarium spp.) persists as a major unmet need.

Identifiants

pubmed: 34986246
pii: 6497801
doi: 10.1093/cid/ciab1070
doi:

Substances chimiques

Antifungal Agents 0
Azoles 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

534-544

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interest. F. L. has received research grants from the Swiss National Science Foundation, the Santos-Suarez Foundation, Novartis, Pfizer, and Merck and has participated on advisory boards for Gilead and Pfizer. R. E. L. has received research grants from Merck and Gilead; has participated on advisory boards for Gilead and Cidara therapeutics; and reports consulting fees from Cidara Therapeutics and F2G Therapeutics. D. P. K. has received research support from Astellas, Merck, T2 Biosystems, Pfizer, and Gilead and honoraria from Merck, Astellas, Gilead, and Cidara; serves on data review committee for Cidara, Scynegis, and AbbVie; and has received consulting fees from Amplyx, Scynexis, Jazz Pharmaceuticals, and Gilead. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Frederic Lamoth (F)

Infectious Diseases Service and Institute of Microbiology, University Hospital of Lausanne and Lausanne University, Lausanne, Switzerland.

Russell E Lewis (RE)

Clinic of Infectious Diseases, S'Orsola-Malpighi Hospital, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italyand.

Dimitrios P Kontoyiannis (DP)

Department of Infectious Diseases, Infection Control and Employee Health, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

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Classifications MeSH