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PMID: 17251531 Published · ppublish English Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Posaconazole vs. fluconazole or itraconazole prophylaxis in patients with neutropenia.

The New England journal of medicine ·Vol. 356 ·No. 4 ·2007-01-25 ·Pages 348-59

Cornely OA, Maertens J, Winston DJ, Perfect J, Ullmann AJ, Walsh TJ, Helfgott D, Holowiecki J, Stockelberg D, Goh YT, Petrini M, Hardalo C, Suresh R, Angulo-Gonzalez D

Abstract

Patients with neutropenia resulting from chemotherapy for acute myelogenous leukemia or the myelodysplastic syndrome are at high risk for difficult-to-treat and often fatal invasive fungal infections. In this randomized, multicenter study involving evaluators who were unaware of treatment assignments, we compared the efficacy and safety of posaconazole with those of fluconazole or itraconazole as prophylaxis for patients with prolonged neutropenia. Patients received prophylaxis with each cycle of chemotherapy until recovery from neutropenia and complete remission, until occurrence of an invasive fungal infection, or for up to 12 weeks, whichever came first. We compared the incidence of proven or probable invasive fungal infections during treatment (the primary end point) between the posaconazole and fluconazole or itraconazole groups; death from any cause and time to death were secondary end points. A total of 304 patients were randomly assigned to receive posaconazole, and 298 patients were randomly assigned to receive fluconazole (240) or itraconazole (58). Proven or probable invasive fungal infections were reported in 7 patients (2%) in the posaconazole group and 25 patients (8%) in the fluconazole or itraconazole group (absolute reduction in the posaconazole group, -6%; 95% confidence interval, -9.7 to -2.5%; P<0.001), fulfilling statistical criteria for superiority. Significantly fewer patients in the posaconazole group had invasive aspergillosis (2 [1%] vs. 20 [7%], P<0.001). Survival was significantly longer among recipients of posaconazole than among recipients of fluconazole or itraconazole (P=0.04). Serious adverse events possibly or probably related to treatment were reported by 19 patients (6%) in the posaconazole group and 6 patients (2%) in the fluconazole or itraconazole group (P=0.01). The most common treatment-related adverse events in both groups were gastrointestinal tract disturbances. In patients undergoing chemotherapy for acute myelogenous leukemia or the myelodysplastic syndrome, posaconazole prevented invasive fungal infections more effectively than did either fluconazole or itraconazole and improved overall survival. There were more serious adverse events possibly or probably related to treatment in the posaconazole group. (ClinicalTrials.gov number, NCT00044486 [ClinicalTrials.gov].).

MeSH Terms
Adolescent Adult Aged Aged, 80 and over Antifungal Agents/adverse effects,therapeutic use Antineoplastic Agents/adverse effects Female Fluconazole/adverse effects,therapeutic use Humans Itraconazole/adverse effects,therapeutic use Kaplan-Meier Estimate Leukemia, Myeloid, Acute/complications,drug therapy,mortality Male Middle Aged Mycoses/mortality,prevention & control Myelodysplastic Syndromes/complications,drug therapy,mortality Neutropenia/chemically induced,drug therapy,mortality Opportunistic Infections/prevention & control Single-Blind Method Treatment Outcome Triazoles/adverse effects,therapeutic use
Chemicals
Antifungal Agents Antineoplastic Agents Triazoles Itraconazole posaconazole Fluconazole
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Cornely Oliver A
University of Cologne, Cologne, Germany. oliver.cornely@uni-koeln.de
Maertens Johan
Winston Drew J
Perfect John
Ullmann Andrew J
Walsh Thomas J
Helfgott David
Holowiecki Jerzy
Stockelberg Dick
Goh Yeow-Tee
Petrini Mario
Hardalo Cathy
Suresh Ramachandran
Angulo-Gonzalez David
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2007-01-25
Pages
348-59
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Databases
ClinicalTrials.gov
NCT00044486
Corrections
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