An open label randomized controlled trial of tamoxifen combined with amphotericin B and fluconazole for cryptococcal meningitis

Author:

Ngan Nguyen Thi Thuy12,Thanh Hoang Le Nhat2,Vi Vi Nguyen Ngo2,Van Ninh Thi Thanh2,Mai Nguyen Thi Hoang2,Van Anh Duong2,Trieu Phan Hai2,Lan Nguyen Phu Huong3,Phu Nguyen Hoan2,Chau Nguyen Van Vinh3,Lalloo David G4,Hope William5,Beardsley Justin67,White Nicholas J89ORCID,Geskus Ronald29,Thwaites Guy E29ORCID,Krysan Damian10,Tai Luong Thi Hue3,Kestelyn Evelyne29ORCID,Binh Tran Quang1,Hung Le Quoc1,Tung Nguyen Le Nhu3,Day Jeremy N29ORCID

Affiliation:

1. Department of Tropical Medicine, Cho Ray Hospital, Ho Chi Minh City, Viet Nam

2. Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

3. The Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam

4. Liverpool School of Tropical Medicine, Liverpool, United Kingdom

5. Centre of Excellence in Infectious Disease Research, Institute of Translational Medicine, Liverpool University, Liverpool, United Kingdom

6. The University of Sydney, Marie Bashir Institute, NSW, Camperdown, Australia

7. Westmead Institute for Medical Research, Westmead, Australia

8. Mahidol Oxford Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

9. Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

10. Department of Paediatrics and Microbiology/Immunology, Carver College of Medicine, University of Iowa, Iowa City, United States

Abstract

Background:Cryptococcal meningitis has high mortality. Flucytosine is a key treatment but is expensive and rarely available. The anticancer agent tamoxifen has synergistic anti-cryptococcal activity with amphotericin in vitro. It is off-patent, cheap, and widely available. We performed a trial to determine its therapeutic potential.Methods:Open label randomized controlled trial. Participants received standard care – amphotericin combined with fluconazole for the first 2 weeks – or standard care plus tamoxifen 300 mg/day. The primary end point was Early Fungicidal Activity (EFA) – the rate of yeast clearance from cerebrospinal fluid (CSF). Trial registration https://clinicaltrials.gov/ct2/show/NCT03112031.Results:Fifty patients were enrolled (median age 34 years, 35 male). Tamoxifen had no effect on EFA (−0.48log10 colony-forming units/mL/CSF control arm versus −0.49 tamoxifen arm, difference −0.005log10CFU/ml/day, 95% CI: −0.16, 0.15, p=0.95). Tamoxifen caused QTc prolongation.Conclusions:High-dose tamoxifen does not increase the clearance rate of Cryptococcus from CSF. Novel, affordable therapies are needed.Funding:The trial was funded through the Wellcome Trust Asia Programme Vietnam Core Grant 106680 and a Wellcome Trust Intermediate Fellowship to JND grant number WT097147MA.

Funder

Wellcome Trust

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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