A randomized trial of itraconazole in allergic bronchopulmonary aspergillosis.

被引:342
作者
Stevens, DA
Schwartz, HJ
Lee, JY
Moskovitz, BL
Jerome, DC
Catanzaro, A
Bamberger, DM
Weinmann, AJ
Tuazon, CU
Judson, MA
Platts-Mills, TAE
DeGraff, AC
Grossman, J
Slavin, RG
Reuman, P
机构
[1] Santa Clara Valley Med Ctr, Dept Med, San Jose, CA 95128 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Infect Dis & Geog Med, Stanford, CA USA
[3] NIAID, Mycoses Study Grp, NIH, Bethesda, MD USA
[4] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[5] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[6] Univ Alabama, Birmingham, AL USA
[7] Janssen Pharmaceut, Titusville, NJ USA
[8] Vet Affairs Med Ctr, Long Beach, CA USA
[9] Univ Missouri, Sch Med, Dept Med, Kansas City, MO 64108 USA
[10] Wayne State Univ, Div Infect Dis, Detroit, MI USA
[11] George Washington Univ, Med Ctr, Washington, DC 20037 USA
[12] Med Univ S Carolina, Div Pulm & Crit Care, Charleston, SC USA
[13] Univ Virginia, Dept Med, Charlottesville, VA USA
[14] Univ Connecticut, Dept Med, Hartford, CT 06112 USA
[15] Vivra Res, Tucson, AZ USA
[16] St Louis Univ, Sch Med, St Louis, MO USA
[17] NIAID, Mycoses Study Grp, NIH, Bethesda, MD USA
关键词
D O I
10.1056/NEJM200003163421102
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Allergic bronchopulmonary aspergillosis is a hypersensitivity disorder that can progress from an acute phase to chronic disease. The main treatment is systemic corticosteroids, but data from uncontrolled studies suggest that itraconazole, an orally administered antifungal agent, may be an effective adjunctive therapy. Methods: We conducted a randomized, double-blind trial of treatment with either 200 mg of itraconazole twice daily or placebo for 16 weeks in patients who met immunologic and pulmonary-function criteria for corticosteroid-dependent allergic bronchopulmonary aspergillosis. A response was defined as a reduction of at least 50 percent in the corticosteroid dose, a decrease of at least 25 percent in the serum IgE concentration, and one of the following: an improvement of at least 25 percent in exercise tolerance or pulmonary-function tests or resolution or absence of pulmonary infiltrates. In a second, open-label part of the trial, all the patients received 200 mg of itraconazole per day for 16 weeks. Results: There were responses in 13 of 28 patients in the itraconazole group (46 percent), as compared with 5 of 27 patients in the placebo group (19 percent, P=0.04). The rate of adverse events was similar in the two groups. In the subsequent open-label phase, 12 of the 33 patients who had not had a response during the double-blind phase (36 percent) had responses, and none of the patients who had a response in the double-blind phase of the trial had a relapse. Conclusions: For patients with corticosteroid-dependent allergic bronchopulmonary aspergillosis, the addition of itraconazole can lead to improvement in the condition without added toxicity. (N Engl J Med 2000;342:756-62.) (C)2000, Massachusetts Medical Society.
引用
收藏
页码:756 / 762
页数:7
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