TY - JOUR
T1 - Micafungin versus caspofungin for treatment of candidemia and other forms of invasive candidiasis
AU - Pappas, Peter G.
AU - Rotstein, Coleman M.F.
AU - Betts, Robert F.
AU - Nucci, Marcio
AU - Talwar, Deepak
AU - De Waele, Jan J.
AU - Vazquez, Jose A.
AU - Dupont, Bertrand F.
AU - Horn, David L.
AU - Ostrosky-Zeichner, Luis
AU - Reboli, Annette C.
AU - Suh, Byungse
AU - Digumarti, Raghunadharao
AU - Wu, Chunzhang
AU - Kovanda, Laura L.
AU - Arnold, Leah J.
AU - Buell, Donald N.
N1 - Funding Information:
Potential conflicts of interest. P.G.P. receives grant support and is on the speaker’s bureaus of Astellas Pharma US, Merck, Pfizer, Enzon, and Schering-Plough. C.M.F.R. is a consultant for and on the speaker’s bureaus of Astellas, Merck-Frosst Canada, and Pfizer and receives grant support from Astellas Pharma US, Merck, and Pfizer. M.N. is a consultant for, is on the speakers’ bureaus of, and receives grant support from Pfizer, Merck, and Schering-Plough. D.H. receives research funding from, is a consultant for, and is on the speakers’ bureaus of Pfizer and Astellas. L.O.Z. receives grant support from, is on the speaker’s bureaus of, and served as a consultant for Astellas, Merck Pfizer, Enzon, and Gilead. AR receives research support from Merck and Pfizer, is on the speakers’ bureau of Pfizer, and is a consultant for Astellas. B.D. is on the speakers’ bureaus of Astellas, Schering-Plough, Cephalon, Merck, and BioAlliance. J.V. is on speakers bureaus of Pfizer, Schering-Plough, and Enzon; receives research support from Pfizer, Astellas, Merck, Salix, Schering-Plough, Johnson and Johnson, Basilea, Bayer, Peninsula, ACC, GlaxoSmithKline, Roche, BioAlliance, Theravance, Wyeth, and Novartis; and is a consultant for Schering-Plough, Astellas, Pfizer, and Smith & Nephew. C.W., L.J.A., L.L.K., and D.N.B. are employees of Astellas. All other authors: no conflicts.
PY - 2007
Y1 - 2007
N2 - Background. Invasive candidiasis is an important cause of morbidity and mortality among patients with health care-associated infection. The echinocandins have potent fungicidal activity against most Candida species, but there are few data comparing the safety and efficacy of echinocandins in the treatment of invasive candidiasis. Methods. This was an international, randomized, double-blind trial comparing micafungin (100 mg daily) and micafungin (150 mg daily) with a standard dosage of caspofungin (70 mg followed by 50 mg daily) in adults with candidemia and other forms of invasive candidiasis. The primary end point was treatment success, defined as clinical and mycological success at the end of blinded intravenous therapy. Results. A total of 595 patients were randomized to one the treatment groups and received at least 1 dose of study drug. In the modified intent-to-treat population, 191 patients were assigned to the micafungin 100 mg group, 199 to the micafungin 150 mg group, and 188 to the caspofungin group. Demographic characteristics and underlying disorders were comparable across the groups. Approximately 85% of patients had candidemia; the remainder had noncandidemic invasive candidiasis. At the end of blinded intravenous therapy, treatment was considered successful for 76.4% of patients in the micafungin 100 mg group, 71.4% in the micafungin 150 mg group, and 72.3% in the caspofungin group. The median time to culture negativity was 2 days in the micafungin 100 mg group and the caspofungin group, compared with 3 days in the micafungin 150 mg groups. There were no significant differences in mortality, relapsing and emergent infections, or adverse events between the study arms. Conclusions. Dosages of micafungin 100 mg daily and 150 mg daily were noninferior to a standard dosage of caspofungin for the treatment of candidemia and other forms of invasive candidiasis.
AB - Background. Invasive candidiasis is an important cause of morbidity and mortality among patients with health care-associated infection. The echinocandins have potent fungicidal activity against most Candida species, but there are few data comparing the safety and efficacy of echinocandins in the treatment of invasive candidiasis. Methods. This was an international, randomized, double-blind trial comparing micafungin (100 mg daily) and micafungin (150 mg daily) with a standard dosage of caspofungin (70 mg followed by 50 mg daily) in adults with candidemia and other forms of invasive candidiasis. The primary end point was treatment success, defined as clinical and mycological success at the end of blinded intravenous therapy. Results. A total of 595 patients were randomized to one the treatment groups and received at least 1 dose of study drug. In the modified intent-to-treat population, 191 patients were assigned to the micafungin 100 mg group, 199 to the micafungin 150 mg group, and 188 to the caspofungin group. Demographic characteristics and underlying disorders were comparable across the groups. Approximately 85% of patients had candidemia; the remainder had noncandidemic invasive candidiasis. At the end of blinded intravenous therapy, treatment was considered successful for 76.4% of patients in the micafungin 100 mg group, 71.4% in the micafungin 150 mg group, and 72.3% in the caspofungin group. The median time to culture negativity was 2 days in the micafungin 100 mg group and the caspofungin group, compared with 3 days in the micafungin 150 mg groups. There were no significant differences in mortality, relapsing and emergent infections, or adverse events between the study arms. Conclusions. Dosages of micafungin 100 mg daily and 150 mg daily were noninferior to a standard dosage of caspofungin for the treatment of candidemia and other forms of invasive candidiasis.
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U2 - 10.1086/520980
DO - 10.1086/520980
M3 - Article
C2 - 17806055
AN - SCOPUS:34848928703
SN - 1058-4838
VL - 45
SP - 883
EP - 893
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 7
ER -