Breakthrough zygomycosis after voriconazole administration among patients with hematologic malignancies who receive hematopoietic stem-cell transplants or intensive chemotherapy

被引:154
作者
Trifilio, S. M.
Bennett, C. L.
Yarnold, P. R.
McKoy, J. M.
Parada, J.
Mehta, J.
Chamilos, G.
Palella, F.
Kennedy, L.
Mullane, K.
Tallman, M. S.
Evens, A.
Scheetz, M. H.
Blum, W.
Kontoyiannis, D. P.
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Dept Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Dept Pharm, Chicago, IL 60611 USA
[3] Jesse Brown VA Med Ctr, Ctr Hlth Serv Res & Policy Studies, Chicago, IL USA
[4] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Dept Med, Chicago, IL USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Emergency Med, Chicago, IL USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Med Div Geriatr Med, Chicago, IL USA
[7] Hines VA Hosp, Midwest Ctr Hlth Serv, Hines, IL USA
[8] Hines VA Hosp, Policy Res & Med Neurol Serv Line, Hines, IL USA
[9] Loyola Univ, Stritch Sch Med, Dept Med, Div Infect Dis, Maywood, IL USA
[10] Univ Texas, MD Anderson Canc Ctr, Houston, TX USA
[11] Northwestern Univ, Feinberg Sch Med, Div Infect Dis, Dept Med, Chicago, IL USA
[12] Wake Forest Univ Hosp, Dept Pharm, Salem, NC USA
[13] Loyola Univ, Stritch Sch Med, Div Infect Dis, Dept Med, Maywood, IL USA
[14] Ohio State Univ, Ctr Med, Div Hematol Oncol, Dept Med, Columbus, OH USA
[15] Univ Texas, MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX USA
关键词
zygomycosis; voriconazole; breakthrough; prophylaxis; leukemia; stem cell transplantation;
D O I
10.1038/SJ.BMT.1705614
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Zygomycosis is increasingly reported as a cause of life-threatening fungal infections. A higher proportion of cases reported over the last decades have been in cancer patients, with or without hematopoietic stem cell transplantation (HSCT). The new anti-fungal agent voriconazole is a recently identified risk factor for developing zygomycosis. We reviewed the clinical characteristics and outcomes of a large cohort of cancer patients who developed zygomycosis after exposure to voriconazole. Health care professionals at 13 large cancer centers provided clinical information on cancer patients with zygomycosis and prior exposure to voriconazole. Criteria for inclusion were 5 days or more of voriconazole use and diagnostic confirmation with tissue or histology. Fifty-eight cases were identified among patients with hematologic malignancies, 62% including patients who underwent a HSCT procedure. Fifty-six patients received voriconazole for primary or secondary prophylaxis against fungal infection. In addition to prior exposure to voriconazole, patients also had several of the previously established risk factors for zygomycosis. Amphotericin B was the most commonly prescribed anti-fungal therapy. Overall mortality was 73%. We conclude that zygomycosis after exposure to voriconazole is a recently described entity that is frequently fatal, despite treatment with currently available anti-fungal agents and surgery.
引用
收藏
页码:425 / 429
页数:5
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