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Forum Report: Issues in the Design of Trials of Drugs for the Treatment of Invasive Aspergillosis
Author(s) -
John E. Bennett,
John H. Powers,
Ben de Pauw,
William E. Dismukes,
John N. Galgiani,
M. P. Glauser,
Raoul Herbrecht,
Carol A. Kauffman,
Jeannette Y. Lee,
Peter G. Pappas,
John Rex,
Paul E. Verweij,
Claudio Viscoli,
Thomas J. Walsh
Publication year - 2003
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/367838
Subject(s) - aspergillosis , medicine , clinical trial , intensive care medicine , antifungal , antifungal drug , clinical study design , drug , antifungal drugs , pharmacology , dermatology , immunology
A recent trial of drugs for invasive aspergillosis was used as a background for discussing critical features in the design of antifungal trials. The study under discussion allowed stopping either drug without classifying the patient as having treatment failure, so the trial should be understood as a comparison of 2 treatment strategies, not just 2 drugs. Although the study was a noninferiority trial, the outcome permitted a claim of superiority. Use of the category of "probable" in addition to "proven" aspergillosis permitted inclusion of patients for whom the diagnosis was less certain but who were still early enough in the disease progression to respond to therapy. Different opinions still exist about some of the criteria for the diagnosis of "probable" aspergillosis. A blinded data review committee was helpful in evaluating efficacy in this unblinded trial but had limited value in assessing toxicity. An understanding of these features of design of antifungal drug trials is important in applying the results to clinical practice.

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