NLM Gateway
A service of the U.S. National Institutes of Health
Your Entrance to
Resources from the
National Library of Medicine
    Home      Term Finder      Limits/Settings      Search Details      History      My Locker        About      Help      FAQ    
Skip Navigation Side Barintended for web crawlers only

Ambisome (A) Versus Fluconazole + Itraconazole (FI) Prophylaxis in Frontline Therapy of Acute Myelogenous Leukemia (AML) and Myelodysplastic Syndrome (MDS).

MATTIUZZI GN, BLAMBLE D, ESTEY E, KWARI M, CORTES J, GILES F, KANTARJIAN H; Interscience Conference on Antimicrobial Agents and Chemotherapy.

Abstr Intersci Conf Antimicrob Agents Chemother Intersci Conf Antimicrob Agents Chemother. 2000 Sep 17-20; 40: 363.

MD Anderson Cancer Ctr., Univ. of Texas, Houston, TX

BACKGROUND: Suspected/proven fungal infections (FI) remain a major cause of morbidity/mortality in patients (pts) with AML and MDS undergoing induction chemotherapy (IC). FI is the standard antifungal prophylaxis (AP) used at MDACCC for these pts. Objective: Evaluate the efficacy and toxicity of A vs. FI in pts with AML/MDS undergoing IC. Method: Prospective, randomized, open-label comparative study. Inclusion criteria: untreated AML or MDS, age [3] 15 y.o., Zubrod 3, creatinine 2 mg%, Bilirubin 2 mg%. Pts were randomized to receive either F400 mg POBID + I200 mgPOBID or A 3 mg/kg IV 3x/week.RESULTS: Seventy-three pts in A and 67 pts in FI were evaluable. Median age was 63 vs. 57 respectively, p=.01. Study groups were comparable in terms of perf. status, median WBC, early risk for mortality and chemotherapy. Twenty-three percent and 36% of the pts had MDS (A and FI respectively). Overall, 44% completed their AP. Thirty-two percent of the pts on A and 35% pts on FI were changed to antifungal therapy because persistent FUO (p=ns). Only 5/140 pts developed FI. In the A group 1 pt developed cellulitis (T. glabrata, C. tropicalis and fusarium), and 2 pts had candidemia (T. glabrata + C. albicans and Parapsilopsis, respectively). One pt on FI developed A. fumigatus sinusitis, other had C. tropicalis candidemia. Thirty percent of the pts on A developed pneumonia of unknown pathogen (PUP) vs. 25% pts on FI. Increase of creatinine 2.0 mg (23% vs. 3%; p=.00) and increase of bilirubin 2.0 mg (23% vs. 9%; p=.04) occurred more often with A prophylaxis. Other adverse events were similar in frequency and rare. Response to IC and induction mortality rates were similar as were survival rates.CONCLUSIONS: A and FI prophylaxis provide similar efficacy in relation to documented FI, PUP, induction mortality, CR and long term outcome in pts with AML/MDS undergoing IC. A was associated with higher incidence of increased bilirubin and creatinine.KEYWORDS: Antifungal; Leukemia; Prophylaxis

Publication Types:
  • Meeting Abstracts
Keywords:
  • AmBisome
  • Amphotericin B
  • Antifungal Agents
  • Antineoplastic Combined Chemotherapy Protocols
  • Bone Marrow Transplantation
  • Fluconazole
  • Humans
  • Itraconazole
  • Leukemia
  • Leukemia, Myeloid, Acute
  • Longitudinal Studies
  • Mycoses
  • Preleukemia
  • Remission Induction
  • drug therapy
  • prevention & control
  • surgery
  • therapy
  • transplantation
Other ID:
  • GWAIDS0009840
UI: 102247338

From Meeting Abstracts




Contact Us
U.S. National Library of Medicine |  National Institutes of Health |  Health & Human Services
Privacy |  Copyright |  Accessibility |  Freedom of Information Act |  USA.gov