Forum report: Issues in the design of trials of drugs for the treatment of invasive aspergillosis

被引:7
|
作者
Bennett, JE
Powers, J
de Pauw, B
Dismukes, W
Galgiani, J
Glauser, M
Herbrecht, R
Kauffman, C
Lee, J
Pappas, P
Rex, J
Verweij, P
Viscoli, C
Walsh, T
机构
[1] NIAID, Clin Mycol Sect, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
[2] NCI, NIH, Bethesda, MD 20892 USA
[3] US FDA, Div Special Pathogen & Immunol Drug Prod, Rockville, MD USA
[4] Univ Alabama, Birmingham, AL USA
[5] VA Med Ctr, Tucson, AZ USA
[6] Univ Arizona, Tucson, AZ USA
[7] VA Med Ctr, Ann Arbor, MI USA
[8] Univ Michigan, Ann Arbor, MI 48109 USA
[9] Univ Texas, Sch Med, Houston, TX USA
[10] Univ Nijmegen St Radboud Hosp, NL-6500 HB Nijmegen, Netherlands
[11] Univ Lausanne Hosp, Lausanne, Switzerland
[12] Hop Hautepierre, Strasbourg, France
[13] Univ Genoa, Natl Inst Canc Res, I-16126 Genoa, Italy
关键词
D O I
10.1086/367838
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:S113 / S116
页数:4
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