Safety and Outcomes of Open-Label Deferasirox Iron Chelation Therapy for Mucormycosis

被引:75
作者
Spellberg, Brad [1 ,2 ]
Andes, David [3 ,4 ]
Perez, Mario [5 ]
Anglim, Anne [6 ]
Bonilla, Hector [7 ]
Mathisen, Glenn E. [8 ]
Walsh, Thomas J. [9 ]
Ibrahim, Ashraf S. [1 ,2 ]
机构
[1] Harbor Univ Calif LosAngeles, Div Infect Dis, Los Angeles Biomed Res Inst, Med Ctr, Torrance, CA USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Wisconsin, Sch Med, Dept Med, Madison, WI USA
[4] Univ Wisconsin, Sch Med, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
[5] Univ So Calif, Sch Med, Dept Med, Div Infect Dis, Los Angeles, CA 90033 USA
[6] Long Beach Publ Dept Hlth, Long Beach, CA USA
[7] Summa Hlth Syst, Akron, OH USA
[8] Olive View UCLA, Med Ctr, Div Infect Dis, Sylmar, CA USA
[9] NCI, Immunocompromised Host Sect, Pediat Oncol Branch, NIH, Bethesda, MD 20892 USA
关键词
AGENT; DEFEROXAMINE; ZYGOMYCOSIS; MANAGEMENT;
D O I
10.1128/AAC.00361-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We sought to describe the safety profile of open-label, adjunctive deferasirox iron chelation therapy in eight patients with biopsy-proven mucormycosis. Deferasirox was administered for an average of 14 days (range, 7 to 21) at 5 to 20 mg/kg of body weight/day. The only adverse effects attributable to deferasirox were rashes in two patients. Deferasirox treatment was not associated with changes in renal or liver function, complete blood count, or transplant immunosuppressive levels. Thus, deferasirox appears safe as an adjunctive therapy for mucormycosis.
引用
收藏
页码:3122 / 3125
页数:4
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