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April 2000, Volume 25, Number 8, Pages 853-859
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Infections Post Transplant
Fluconazole vs low-dose amphotericin B for the prevention of fungal infections in patients undergoing bone marrow transplantation: a study of the North American Marrow Transplant Group
S N Wolff1, J Fay2, D Stevens3, R H Herzig4, B Pohlman5, B Bolwell5, J Lynch6, S Ericson6, C O Freytes7, F LeMaistre7, R Collins2, L Pineiro2, J Greer1, R Stein1, S A Goodman1 and S Dummer1

1Vanderbilt University, Nashville, TN, USA

2Baylor University Medical Center, Dallas, TX, USA

3University of Louisville, Louisville, KY, USA

4Jewish Hospital, Cincinnati, OH, USA

5Cleveland Clinic, Cleveland, OH, USA

6West Virginia University, Morgantown, WV, USA

7University of Texas Health Science Center at San Antonio, San Antonio, TX, USA

Correspondence to: Dr S N Wolff, Bone Marrow Transplant Program, 2617 TVC, Vanderbilt University, Nashville, TN 37232-5505, USA

Abstract

systemic fungal infections are a major problem in bone marrow transplant recipients who have prolonged neutropenia or who receive high-dose corticosteroids. prophylaxis with fluconazole or low-dose amphotericin b reduces, but does not eliminate these infections. to determine which prophylactic agent is better, we performed a prospective randomized study. patients undergoing allogeneic (related or unrelated) or autologous marrow or peripheral stem cell transplantation were randomized to receive fluconazole (400 mg/day p.o. or i.v.) or amphotericin b (0.2 mg/kg/day i.v.) beginning 1 day prior to stem cell transplantation and continuing until recovery of neutrophils to >500/mul. patients were removed from their study drug for drug-associated toxicity, invasive fungal infection or suspected fungal infection (defined as the presence of fever >38°C without positive culture while on broad-spectrum anti-bacterial antibiotics). Proven or suspected fungal infections were treated with high-dose amphotericin B (0.5-0.7 mg/kg/day). Patients were randomized at each institution and stratified for the type of transplant. The primary end-point of the study was prevention of documented fungal infection; secondary endpoints included fungal colonization, drug toxicity, duration of hospitalization, duration of fever, duration of neutropenia, duration and total dose of high-dose amphotericin B and overall survival to hospital discharge. From July 1992 to October 1994, a total of 355 patients entered into the trial with 159 patients randomized to amphotericin B and 196 to Fluconazole. Patient groups were comparable for diagnosis, age, sex, prior antibiotic or antifungal therapy, use of corticosteroids prior to transplantation and total duration of neutropenia. Amphotericin B was significantly more toxic than Fluconazole especially in related allogeneic transplantation where 19% of patients developed toxicity vs 0% of Fluconazole recipients (p < 0.05). approximately 44% of all patients were removed from prophylaxis for presumed fungal infection. proven fungal infections occurred in 4.1% and 7.5% of fluconazole and amphotericin-treated patients, respectively. proven fungal infections occurred in 9.1% and 14.3% of related allogeneic marrow recipients receiving fluconazole or amphotericin b, respectively, and 2.1% and 5.6% of autologous marrow recipients receiving fluconazole or amphotericin b, respectively (P > 0.05). In this prospective trial, low-dose amphotericin B prophylaxis was as effective as Fluconazole prophylaxis, but Fluconazole was significantly better tolerated. Bone Marrow Transplantation (2000) 25 , 853-859.

Keywords

fungal infection prophylaxis; Fluconazole; amphotericin B

Received 11 August 1999; accepted 2 November 1999
April 2000, Volume 25, Number 8, Pages 853-859
Table of contents    Previous  Abstract  Next   Full text  PDF
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