Optimizing the Treatment of Invasive Candidiasis—A Case for Combination Therapy

Author:

Wake Rachel M12ORCID,Allebone-Salt Phoebe E12,John Larissa L H3,Caswall Ben A1,Govender Nelesh P14563,Ben-Ami Ronen7,Murray Lyle W8,Logan Clare12,Harrison Thomas S123,Bicanic Tihana A123

Affiliation:

1. Institute for Infection and Immunity, St George's University of London , London , UK

2. Clinical Academic Group, St George's Hospital NHS Trust , London , UK

3. MRC Centre for Medical Mycology, University of Exeter , Exeter , UK

4. National Institute for Communicable Diseases, A Division of the National Health Laboratory Service , Johannesburg , South Africa

5. School of Pathology, University of Witwatersrand , Johannesburg , South Africa

6. Institute of Infectious Disease and Molecular Medicine, University of Cape Town , Cape Town , South Africa

7. Infectious Diseases Unit, Tel-Aviv Sourasky Medical Center, and the Sackler , Tel-Aviv , Israel

8. Division of Infectious Diseases, Department of Internal Medicine, University of the Witwatersrand , Johannesburg , South Africa

Abstract

Abstract Invasive candidiasis is a rising global health threat with increasing incidence, persistently high mortality, and diminishing treatment options. Antifungal resistance has rapidly emerged and spread, with multidrug-resistant species deemed an urgent and serious threat. While acknowledging the key role of antifungal stewardship and infection control in curbing spread, we examine the role of antifungal monotherapy in driving resistance and the potential for combination therapy to prevent stress adaptation and emergence of drug resistance. In addition to its role in mitigating resistance, combination treatment may improve drug penetration, expedite fungal clearance, and allow lower, less toxic doses of individual drugs to be used. A growing body of laboratory-based evidence suggests that antifungal combinations can yield synergistic activity against Candida spp., including against frequently multidrug-resistant Candida auris. It is imperative to test these combinations in clinical trials, incorporating resistance end points as a marker of success.

Funder

NIHR Clinical Lectureship

NIHR

UK Government

Gilead UK & Ireland

NIHR BRC

Publisher

Oxford University Press (OUP)

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