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Higher Dose Oral Fluconazole for the Treatment of AIDS-related Cryptococcal Meningitis (HIFLAC)—report of A5225, a multicentre, phase I/II, two-stage, dose-finding, safety, tolerability and efficacy randomised, amphotericin B-controlled trial of the AIDS Clinical Trials Group

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dc.contributor.author LallooI, Umesh G.
dc.contributor.author Komarow, Lauren
dc.contributor.author AbergI, Judith A.
dc.contributor.author Clifford, David B.
dc.contributor.author Hogg, Evelyn
dc.contributor.author McKhann, Ashley
dc.contributor.author Bukuru, Aggrey
dc.contributor.author Pillay, Sandy
dc.contributor.author Mave, Vidya
dc.contributor.author Supparatpinyo, Khuanchai
dc.contributor.author Samaneka, Wadzanai
dc.contributor.author Langat, Deborah
dc.contributor.author Ticona, Eduardo
dc.contributor.author Badal-Faesen, Sharlaa
dc.date.accessioned 2024-05-09T13:29:25Z
dc.date.available 2024-05-09T13:29:25Z
dc.date.issued 2023-02-13
dc.identifier.uri https://doi.org/10.1371/journal.pone.0281580
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/9080
dc.description.abstract Background The WHO recommended 1200mg/day of fluconazole (FCZ) in the induction phase of crypto- coccal meningitis (CM) in HIV prior to 2018 in regions where amphotericin-B (AMB) was unavailable. A 2-stage AMB-controlled, dose-escalation study to determine the maximum tolerated dose and the safety/efficacy of an induction-consolidation strategy of higher doses FCZ (1200mg-2000mg/day), adjusted for weight and renal function (eGFR)in adults with CM was undertaken. Methods In Stage-1, three induction doses of FCZ (1200mg/day, 1600mg/day and 2000mg/day) were tested in sequential cohortsand compared with AMB in a 3:1 ratio. A particular dose was not tested in Stage 2 if there were significant predetermined safety or efficacy concerns.In Stage-2, the 1200mg dose was excluded per protocol because of increased mortality, and participants were randomised to 1600mg, 2000mg FCZ or AMB in a 1:1:1 ratio. Findings One hundred and sixty eight participants were enrolled with 48, 50, and 48 in the AMB, 1600mg and 2000mg cohorts. The Kaplan Meier proportion for mortality (90% CI) at 10 and 24 weeks for AMB was 17% (10, 29) and 24% (15, 37), compared to 20% (12, 32) and 30% (20, 43) for 1600mg, and 33% (23, 46) and 38% (27, 51) for 2000mg/day FCZ. With the exception of a higher incidence of gastrointestinal side effects in the 2000mg cohort, both induction doses of FCZ were safe and well tolerated. There were no life-threatening changes in electrocardiogram QTc which were similar across all doses of FCZ and AMB. The median (IQR) change in log10 cryptoccal colony forming units (CFU) from week 0 to week 2 was -8(-4.1,-1.9) for AMB; -2.5(-4.0, -1.4) for 1600mg FCZ and -8 (-3.2, -1.0) for 2000mg FCZ. The proportion (90% CI) CSF CM negative at 10 weeks was 81%(71,90) for AMB; 56%(45,69) for 1600mg FCZ and 60%(49,73) for 2000mg FCZ. en_US
dc.description.sponsorship UM1 AI068634, UM1 AI068636 and UM1 AI106701; en_US
dc.language.iso en en_US
dc.publisher PLOS ONE en_US
dc.subject Oral Fluconazole en_US
dc.subject Cryptococcal Meningitis en_US
dc.title Higher Dose Oral Fluconazole for the Treatment of AIDS-related Cryptococcal Meningitis (HIFLAC)—report of A5225, a multicentre, phase I/II, two-stage, dose-finding, safety, tolerability and efficacy randomised, amphotericin B-controlled trial of the AIDS Clinical Trials Group en_US
dc.type Article en_US


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