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

      research-article
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      ,
      eLife
      eLife Sciences Publications, Ltd
      cryptococcus neoformans, cryptococcus gattii, HIV, randomised controlled trial, cryptococcal meningitis, Viet Nam, Other

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          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.

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          Most cited references38

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          Global burden of disease of HIV-associated cryptococcal meningitis: an updated analysis.

          Cryptococcus is the most common cause of meningitis in adults living with HIV in sub-Saharan Africa. Global burden estimates are crucial to guide prevention strategies and to determine treatment needs, and we aimed to provide an updated estimate of global incidence of HIV-associated cryptococcal disease.
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            Antifungal Combinations for Treatment of Cryptococcal Meningitis in Africa

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              Combination antifungal therapy for cryptococcal meningitis.

              Combination antifungal therapy (amphotericin B deoxycholate and flucytosine) is the recommended treatment for cryptococcal meningitis but has not been shown to reduce mortality, as compared with amphotericin B alone. We performed a randomized, controlled trial to determine whether combining flucytosine or high-dose fluconazole with high-dose amphotericin B improved survival at 14 and 70 days. We conducted a randomized, three-group, open-label trial of induction therapy for cryptococcal meningitis in patients with human immunodeficiency virus infection. All patients received amphotericin B at a dose of 1 mg per kilogram of body weight per day; patients in group 1 were treated for 4 weeks, and those in groups 2 and 3 for 2 weeks. Patients in group 2 concurrently received flucytosine at a dose of 100 mg per kilogram per day for 2 weeks, and those in group 3 concurrently received fluconazole at a dose of 400 mg twice daily for 2 weeks. A total of 299 patients were enrolled. Fewer deaths occurred by days 14 and 70 among patients receiving amphotericin B and flucytosine than among those receiving amphotericin B alone (15 vs. 25 deaths by day 14; hazard ratio, 0.57; 95% confidence interval [CI], 0.30 to 1.08; unadjusted P=0.08; and 30 vs. 44 deaths by day 70; hazard ratio, 0.61; 95% CI, 0.39 to 0.97; unadjusted P=0.04). Combination therapy with fluconazole had no significant effect on survival, as compared with monotherapy (hazard ratio for death by 14 days, 0.78; 95% CI, 0.44 to 1.41; P=0.42; hazard ratio for death by 70 days, 0.71; 95% CI, 0.45 to 1.11; P=0.13). Amphotericin B plus flucytosine was associated with significantly increased rates of yeast clearance from cerebrospinal fluid (-0.42 log10 colony-forming units [CFU] per milliliter per day vs. -0.31 and -0.32 log10 CFU per milliliter per day in groups 1 and 3, respectively; P<0.001 for both comparisons). Rates of adverse events were similar in all groups, although neutropenia was more frequent in patients receiving a combination therapy. Amphotericin B plus flucytosine, as compared with amphotericin B alone, is associated with improved survival among patients with cryptococcal meningitis. A survival benefit of amphotericin B plus fluconazole was not found. (Funded by the Wellcome Trust and the British Infection Society; Controlled-Trials.com number, ISRCTN95123928.).
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                Author and article information

                Contributors
                Role: Senior Editor
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                28 September 2021
                2021
                : 10
                : e68929
                Affiliations
                [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
                Radboud University Medical Centre Netherlands
                Radboudumc Center for Infectious Diseases Netherlands
                Radboudumc Center for Infectious Diseases Netherlands
                Author information
                http://orcid.org/0000-0002-1897-1978
                http://orcid.org/0000-0002-2858-2087
                http://orcid.org/0000-0002-5728-0918
                https://orcid.org/0000-0002-7843-6280
                Article
                68929
                10.7554/eLife.68929
                8547950
                34581270
                4618a285-5f92-4791-8834-e70ce1854ac1
                © 2021, Ngan et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 30 March 2021
                : 21 September 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: Wellcome Trust Asia Programme Vietnam Core Grant 106680
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: Intermediate Fellowship WT097147MA
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Medicine
                Microbiology and Infectious Disease
                Custom metadata
                Despite evidence of significant anti-cryptococcal activity in vitro and animal models, including synergy with other antifungal agents, high-dose tamoxifen has no impact on cerebrospinal fluid sterilization in cryptococcal meningitis.

                Life sciences
                cryptococcus neoformans,cryptococcus gattii,hiv,randomised controlled trial,cryptococcal meningitis,viet nam,other

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