| Literature DB >> 19039629 |
Yasushi Hiramatsu1, Yoshinobu Maeda1, Nobuharu Fujii1, Takashi Saito2, Yuichiro Nawa3, Masamichi Hara3, Tomofumi Yano4, Shoji Asakura5, Kazutaka Sunami5, Takayuki Tabayashi6, Akira Miyata6, Ken-Ichi Matsuoka1, Katsuji Shinagawa1, Kazuma Ikeda1, Keitaro Matsuo7, Mitsune Tanimoto8,9.
Abstract
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.Entities:
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Year: 2008 PMID: 19039629 DOI: 10.1007/s12185-008-0196-y
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490