TY - JOUR
T1 - Use of micafungin versus fluconazole for antifungal prophylaxis in neutropenic patients receiving hematopoietic stem cell transplantation
AU - Hiramatsu, Yasushi
AU - Maeda, Yoshinobu
AU - Fujii, Nobuharu
AU - Saito, Takashi
AU - Nawa, Yuichiro
AU - Hara, Masamichi
AU - Yano, Tomofumi
AU - Asakura, Shoji
AU - Sunami, Kazutaka
AU - Tabayashi, Takayuki
AU - Miyata, Akira
AU - Matsuoka, Ken Ichi
AU - Shinagawa, Katsuji
AU - Ikeda, Kazuma
AU - Matsuo, Keitaro
AU - Tanimoto, Mitsune
PY - 2009/12
Y1 - 2009/12
N2 - A prospective randomized clinical trial assessed the efficacy and tolerance of micafungin compared with that of standard fluconazole treatment in patients undergoing hematopoietic stem cell transplantation (HSCT). Adult patients (n = 106) were randomly assigned to receive prophylaxis with either micafungin 150 mg (n = 52), or fluconazole 400 mg (n = 52). Success was defined as the absence of suspected, proven, or probable invasive fungal infection (IFI) through the end of therapy and the absence of proven or probable IFI through the end of the 4-week period following treatment. The overall efficacy of micafungin was comparable to that of fluconazole (94 vs. 88%; difference 6.0%; 95% confidence interval, -5.4 to +17.4%; P = 0.295). A total of 2 (4.0%) of 50 patients in the micafungin arm and 6 (12.0%) of 50 patients in the fluconazole arm received empirical antifungal therapy (P = 0.06). Micafungin treatment did not result in increasing adverse effects and had a safe profile as fluconazole in neutropenic patients. This randomized trial indicates that the efficacy and tolerance of micafungin 150 mg was comparable to that of fluconazole 400 mg, suggesting that micafungin at 150 mg daily represents a valuable new treatment option for antifungal prophylaxis in HSCT recipients.
AB - A prospective randomized clinical trial assessed the efficacy and tolerance of micafungin compared with that of standard fluconazole treatment in patients undergoing hematopoietic stem cell transplantation (HSCT). Adult patients (n = 106) were randomly assigned to receive prophylaxis with either micafungin 150 mg (n = 52), or fluconazole 400 mg (n = 52). Success was defined as the absence of suspected, proven, or probable invasive fungal infection (IFI) through the end of therapy and the absence of proven or probable IFI through the end of the 4-week period following treatment. The overall efficacy of micafungin was comparable to that of fluconazole (94 vs. 88%; difference 6.0%; 95% confidence interval, -5.4 to +17.4%; P = 0.295). A total of 2 (4.0%) of 50 patients in the micafungin arm and 6 (12.0%) of 50 patients in the fluconazole arm received empirical antifungal therapy (P = 0.06). Micafungin treatment did not result in increasing adverse effects and had a safe profile as fluconazole in neutropenic patients. This randomized trial indicates that the efficacy and tolerance of micafungin 150 mg was comparable to that of fluconazole 400 mg, suggesting that micafungin at 150 mg daily represents a valuable new treatment option for antifungal prophylaxis in HSCT recipients.
KW - Antifungal prophylaxis
KW - Hematopoietic stem cell transplantation
KW - Micafungin
UR - http://www.scopus.com/inward/record.url?scp=64249152006&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=64249152006&partnerID=8YFLogxK
U2 - 10.1007/s12185-008-0196-y
DO - 10.1007/s12185-008-0196-y
M3 - Article
C2 - 19039629
AN - SCOPUS:64249152006
SN - 0925-5710
VL - 88
SP - 588
EP - 595
JO - International journal of hematology
JF - International journal of hematology
IS - 5
ER -