Safety, tolerability, and feasibility of antifungal prophylaxis with micafungin at 2 mg/kg daily in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation

被引:14
作者
Yoshikawa, K. [1 ]
Nakazawa, Y. [1 ]
Katsuyama, Y. [2 ]
Hirabayashi, K. [1 ]
Saito, S. [1 ]
Shigemura, T. [1 ]
Tanaka, M. [1 ]
Yanagisawa, R. [1 ]
Sakashita, K. [1 ]
Koike, K. [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ Hosp, Dept Pharm, Matsumoto, Nagano, Japan
关键词
Micafungin; Invasive fungal infection; Prophylaxis; Allogeneic hematopoietic stem cell transplantation; INVASIVE FUNGAL-INFECTIONS; DRUG-INTERACTION; RECIPIENTS; TACROLIMUS; CHILDREN; ASPERGILLOSIS; VORICONAZOLE; FLUCONAZOLE; DYSFUNCTION; DISEASE;
D O I
10.1007/s15010-014-0601-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Micafungin (MCFG) is used for the prophylaxis of invasive fungal disease (IFD) after allogeneic hematopoietic stem cell transplantation (HSCT). However, the safety, efficacy, or optimal dosage/blood levels as prophylaxis is uncertain in pediatric HSCT-patients. We prophylactically administered MCFG at 2 mg/kg once daily to 38 children and adolescents undergoing allogeneic HSCT. During MCFG prophylaxis, infusion reactions or adverse events (grades 2-5) related to MCFG use were not found in all the patients. Thus, MCFG prophylaxis was not discontinued and other antifungal agents were not added except for 2 patients in whom probable or possible IFDs developed (completion rate, 94.7 %). To elucidate the influence of HSCT-related complications/drugs on blood concentration of MCFG, we determined the plasma trough and peak levels in 13 and 10 among 38 patients, respectively. The mean trough and peak levels were 3.04 +/- A 1.21 mu g/mL (569 samples) and 9.63 +/- A 3.62 mu g/mL (44 samples), respectively. The peak levels were moderately correlated to the trough levels (R (2) = 0.466). In a patient, the trough level of MCFG transiently increased up to 10.21 mu g/mL during hepatic dysfunction due to acute graft-versus-host disease. The MCFG trough levels strongly correlated with T-Bil value (R (2) = 0.894). There was no relationship between the trough levels of MCFG and the circulating concentrations of tacrolimus (R (2) = 0.040). Additionally, MCFG levels were not influenced by treatment with cyclophosphamide or corticosteroids. Prophylaxis with MCFG at 2 mg/kg once daily may be safe, tolerable, and feasible in pediatric HSCT-patients.
引用
收藏
页码:639 / 647
页数:9
相关论文
共 25 条
[1]   Serious infections after unrelated donor transplantation in 136 children: Impact of stem cell source [J].
Barker, JN ;
Hough, RE ;
van Burik, JAH ;
DeFor, TE ;
MacMillan, ML ;
O'Brien, MR ;
Wagner, JE .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (05) :362-370
[2]   Infections diagnosed in the first year after pediatric stem cell transplantation [J].
Benjamin, DK ;
Miller, WC ;
Bayliff, S ;
Martel, L ;
Alexander, KA ;
Martin, PL .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2002, 21 (03) :227-234
[3]  
Bormann AM, 2009, DRUG DES DEV THER, V3, P295
[4]   Invasive mycoses in children receiving hemopoietic SCT [J].
Castagnola, E. ;
Faraci, M. ;
Moroni, C. ;
Bandettini, R. ;
Granata, C. ;
Caruso, S. ;
Bagnasco, F. ;
Caviglia, I. ;
Malgorzata, M. ;
Furfaro, E. ;
Natalizia, A. R. ;
de Fazio, V. ;
Morreale, G. ;
Lanino, E. ;
Haupt, R. ;
Dini, G. ;
Viscoli, C. .
BONE MARROW TRANSPLANTATION, 2008, 41 (Suppl 2) :S107-S111
[5]  
Chiou C C, 2000, Oncologist, V5, P120, DOI 10.1634/theoncologist.5-2-120
[6]   Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group [J].
De Pauw, Ben ;
Walsh, Thomas J. ;
Donnelly, J. Peter ;
Stevens, David A. ;
Edwards, John E. ;
Calandra, Thierry ;
Pappas, Peter G. ;
Maertens, Johan ;
Lortholary, Olivier ;
Kauffman, Carol A. ;
Denning, David W. ;
Patterson, Thomas F. ;
Maschmeyer, Georg ;
Bille, Jacques ;
Dismukes, William E. ;
Herbrecht, Raoul ;
Hope, William W. ;
Kibbler, Christopher C. ;
Kullberg, Bart Jan ;
Marr, Kieren A. ;
Munoz, Patricia ;
Odds, Frank C. ;
Perfect, John R. ;
Restrepo, Angela ;
Ruhnke, Markus ;
Segal, Brahm H. ;
Sobel, Jack D. ;
Sorrell, Tania C. ;
Viscoli, Claudio ;
Wingard, John R. ;
Zaoutis, Theoklis ;
Bennett, John E. .
CLINICAL INFECTIOUS DISEASES, 2008, 46 (12) :1813-1821
[7]   Risks and outcomes of invasive fungal infections in pediatric patients undergoing allogeneic hematopoietic cell transplantation [J].
Dvorak, CC ;
Steinbach, WJ ;
Brown, JMY ;
Agarwal, R .
BONE MARROW TRANSPLANTATION, 2005, 36 (07) :621-629
[8]   Antifungal prophylaxis in pediatric hematology/oncology: New choices & new data [J].
Dvorak, Christopher C. ;
Fisher, Brian T. ;
Sung, Lillian ;
Steinbach, William J. ;
Nieder, Michael ;
Alexander, Sarah ;
Zaoutis, Theoklis E. .
PEDIATRIC BLOOD & CANCER, 2012, 59 (01) :21-26
[9]   Micafungin Does Not Influence the Concentration of Tacrolimus in Patients After Allogeneic Hematopoietic Stem Cell Transplantation [J].
Fukuoka, N. ;
Imataki, O. ;
Ohnishi, H. ;
Kitanaka, A. ;
Kubota, Y. ;
Ishida, T. ;
Tanaka, T. .
TRANSPLANTATION PROCEEDINGS, 2010, 42 (07) :2725-2730
[10]   Infections in children undergoing allogeneic bone marrow transplantation in India [J].
George, B ;
Mathews, V ;
Viswabandya, A ;
Srivastava, A ;
Chandy, M .
PEDIATRIC TRANSPLANTATION, 2006, 10 (01) :48-54