Treatment of 21 cases of invasive mucormycosis with amphotericin B colloidal dispersion

被引:66
作者
Herbrecht, R [1 ]
Letscher-Bru, V
Bowden, RA
Kusne, S
Anaissie, EJ
Graybill, JR
Noskin, GA
Oppenheim, BA
Andrès, E
Pietrelli, LA
机构
[1] Hop Haute Pierre, Dept Oncohematol, F-67098 Strasbourg, France
[2] Inst Parasitol & Pathol Trop, Strasbourg, France
[3] Providence Seattle Med Ctr, Seattle, WA USA
[4] Univ Pittsburgh, Ctr Med, Pittsburgh, PA USA
[5] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
[6] Northwestern Univ, Sch Med, Chicago, IL USA
[7] Withington Hosp, Manchester M20 8LR, Lancs, England
[8] Hop Haute Pierre, Serv Med Interne, Strasbourg, France
关键词
D O I
10.1007/s10096-001-8152-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The aim of this study was to review the characteristics and outcome of 21 patients with invasive mucormycosis treated with amphotericin B colloidal dispersion (ABCD) in five phase I and phase II studies. Mucormycosis is an increasing concern in immunocompromised patients, in whom mortality exceeds 60%. The standard treatment has been amphotericin B combined with surgical debridement. Twenty-one patients with invasive mucormycosis treated with ABCD, a lipid complex of amphotericin B and cholesteryl sulfate, were identified. Patients were given ABCD on the basis of pre-existing renal insufficiency, development of nephrotoxicity during amphotericin B therapy, or fungal infection that failed to respond to amphotericin B. Response could be evaluated in 20 patients, all of whom had bone marrow or organ transplantation, haematologic malignancies, or diabetes. Infection was disseminated in six patients and localised to the sinuses, lower respiratory tract, or skin in the other patients. ABCD was given at a mean dose of 4.8 mg/kg per infusion for a mean duration of 37 days. Twelve of 20 patients responded to ABCD therapy. Response rates were similar when patients were treated with ABCD alone (4/7) and ABCD combined with surgery (8/13), with more complete response obtained in the latter group. No difference in response rate was observed in leukaemic patients (3/5) or transplant recipients (6/10) compared to diabetics (3/5). No renal or hepatic toxicity was observed. These results compare favourably with the results of standard treatment and suggest that ABCD combined with surgery may be a useful therapy in patients with mucormycosis.
引用
收藏
页码:460 / 466
页数:7
相关论文
共 28 条
[21]   INFECTION DUE TO RHIZOMUCOR-PUSILLUS - REPORT OF 4 CASES IN PATIENTS WITH LEUKEMIA AND REVIEW [J].
STGERMAIN, G ;
ROBERT, A ;
ISHAK, M ;
TREMBLAY, C ;
CLAVEAU, S .
CLINICAL INFECTIOUS DISEASES, 1993, 16 (05) :640-645
[22]   Rhinocerebral mucormycosis - Therapy with amphotericin B lipid complex [J].
Strasser, MD ;
Kennedy, RJ ;
Adam, RD .
ARCHIVES OF INTERNAL MEDICINE, 1996, 156 (03) :337-339
[23]   PULMONARY MUCORMYCOSIS - RESULTS OF MEDICAL AND SURGICAL THERAPY [J].
TEDDER, M ;
SPRATT, JA ;
ANSTADT, MP ;
HEGDE, SS ;
TEDDER, SD ;
LOWE, JE .
ANNALS OF THORACIC SURGERY, 1994, 57 (04) :1044-1050
[24]   TREATMENT OF EXPERIMENTAL ZYGOMYCOSIS IN GUINEA-PIGS WITH AZOLES AND WITH AMPHOTERICIN-B [J].
VANCUTSEM, J ;
VANGERVEN, F ;
FRANSEN, J ;
JANSSEN, PAJ .
CHEMOTHERAPY, 1989, 35 (04) :267-272
[25]  
VandenSaffele JK, 1996, MYCOSES, V39, P77, DOI 10.1111/j.1439-0507.1996.tb00106.x
[26]  
White MH, 1997, CLIN INFECT DIS, V24, P635
[27]   Randomized, double-blind clinical trial of amphotericin B colloidal dispersion vs. amphotericin B in the empirical treatment of fever and neutropenia [J].
White, MH ;
Bowden, RA ;
Sandler, ES ;
Graham, ML ;
Noskin, GA ;
Wingard, JR ;
Goldman, M ;
van Burik, JA ;
McCabe, A ;
Miller, CB ;
Gurwith, M ;
Carole, B .
CLINICAL INFECTIOUS DISEASES, 1998, 27 (02) :296-302
[28]   SURVIVAL FACTORS IN RHINO-ORBITAL-CEREBRAL MUCORMYCOSIS [J].
YOHAI, RA ;
BULLOCK, JD ;
AZIZ, AA ;
MARKERT, RJ .
SURVEY OF OPHTHALMOLOGY, 1994, 39 (01) :3-22