NIAID MYCOSES STUDY-GROUP MULTICENTER TRIAL OF ORAL ITRACONAZOLE THERAPY FOR INVASIVE ASPERGILLOSIS

被引:400
作者
DENNING, DW
LEE, JY
HOSTETLER, JS
PAPPAS, P
KAUFFMAN, CA
DEWSNUP, DH
GALGIANI, JN
GRAYBILL, JR
SUGAR, AM
CATANZARO, A
GALLIS, H
PERFECT, JR
DOCKERY, B
DISMUKES, WE
STEVENS, DA
机构
[1] SANTA CLARA VALLEY MED CTR, DEPT MED, DIV INFECT DIS, SAN JOSE, CA 95128 USA
[2] CALIF INST MED RES, SAN JOSE, CA 95128 USA
[3] STANFORD UNIV, SCH MED, DIV INFECT DIS & GEOG MED, STANFORD, CA 94305 USA
[4] UNIV ALABAMA, CTR COMPREHENS CANC, DIV BIOSTAT, BIRMINGHAM, AL 35294 USA
[5] UNIV ALABAMA, DEPT MED, DIV INFECT DIS, BIRMINGHAM, AL 35294 USA
[6] UNIV MICHIGAN, SCH MED,VET AFFAIRS MED CTR,DEPT INTERNAL MED, DIV INFECT DIS, ANN ARBOR, MI USA
[7] VET AFFAIRS MED CTR, MED SERV, DIV INFECT DIS, TUCSON, AZ USA
[8] UNIV ARIZONA, DEPT MED, TUCSON, AZ USA
[9] AUDIE L MURPHY MEM VET ADM MED CTR, DIV INFECT DIS, SAN ANTONIO, TX 78284 USA
[10] UNIV TEXAS, HLTH SCI CTR, DEPT MED, SAN ANTONIO, TX 78284 USA
[11] BOSTON UNIV, SCH MED, DEPT MED, DIV INFECT DIS, BOSTON, MA 02118 USA
[12] UNIV CALIF SAN DIEGO, DEPT MED, DIV PULM MED, SAN DIEGO, CA 92103 USA
[13] DUKE UNIV, DEPT MED, DIV INFECT DIS, DURHAM, NC USA
关键词
D O I
10.1016/0002-9343(94)90023-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Invasive aspergillosis is the most common invasive mould infection and a major cause of mortality in immunocompromised patients. Response to amphotericin B, the only antifungal agent licensed in the United States for the treatment of aspergillosis, is suboptimal. METHODS: A multicenter open study with strict entry criteria for invasive aspergillosis evaluated oral itraconazole (600 mg/d for 4 days followed by 400 mg/d) in patients with various underlying conditions. Response was based on clinical and radiologic criteria plus microbiology, histopathology, and autopsy data. Responses were categorized as complete, partial, or stable. Failure was categorized as an itraconazole failure or overall failure. RESULTS: Our study population consisted of 76 evaluable patients. Therapy duration varied from 0.3 to 97 weeks (median 46). At the end of treatment, 30 (39%) patients had a complete or partial response, and 3 (4%) had a stable response, and in 20 patients (26%), the protocol therapy was discontinued early (at 0.6 to 54.3 weeks) because of a worsening clinical course or death due to aspergillosis (itraconazole failure). Twenty-three (30%) patients withdrew for other reasons including possible toxicity (7%) and death due to another cause but without resolution of aspergillosis (20%). Itraconazole failure rates varied widely according to site of disease and underlying disease group: 14% for pulmonary and tracheobronchial disease, 50% for sinus disease, 63% for central nervous system disease, and 44% for other sites; 7% in solid organ transplant, 29% in allogeneic bone marrow transplant patients, and 14% in those with prolonged granulocytopenia (median 19 days), 44% in AIDS patients, and 32% in other host groups. The relapse rates among those who completed therapy and those who discontinued early for possible toxicity were 12% and 40%, respectively; all were still immunosuppressed. CONCLUSION: Oral itraconazole is a useful alternative therapy for invasive aspergillosis with response rates apparently comparable to amphotericin B. Relapse in immunocompromised patients may be a problem. Controlled trials are necessary to fully assess the role of itraconazole in the treatment of invasive aspergillosis.
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页码:135 / 144
页数:10
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