Open-label, randomized comparison of itraconazole versus caspofungin for prophylaxis in patients with hematologic malignancies

被引:120
作者
Mattiuzzi, GN
Alvarado, G
Giles, FJ
Ostrosky-Zeichner, L
Cortes, J
O'Brien, S
Verstovsek, S
Faderl, S
Zhou, X
Raad, II
Bekele, BN
Leitz, GJ
Lopez-Roman, I
Estey, EH
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Unit 428, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Infect Dis, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Infect Dis Infect Control, Houston, TX 77030 USA
[5] Univ Texas, Houston Med Sch, Lab Mycol Res, Div Infect Dis,Dept Internal Med, Houston, TX USA
[6] Univ Texas, Houston Med Sch, Ctr Study Emerging & Re Emerging Pathogens, Houston, TX USA
[7] Ortho Biotech Prod LP, Bridgeway, NJ USA
关键词
D O I
10.1128/AAC.50.1.143-147.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Invasive fungal infection remains the most common cause of infectious death in acute leukemia. In this open-label, randomized study, we compared the efficacy and safety of caspofungin with that of intravenous itraconazole for antifungal prophylaxis in patients undergoing induction chemotherapy for acute myelogenous leukemia or myelodysplastic syndrome. Of 200 patients, 192 were evaluable for efficacy (86 for itraconazole, 106 for caspofungin). Duration of prophylaxis (median, 21 days [range, 1 to 38 days]), demographics, and prognostic factors were similar in both groups. Ninety-nine patients completed antifungal prophylaxis without developing fungal infection (44 [51%] with itraconazole, 55 [52%] with caspofungin). Twelve patients developed documented invasive fungal infections, five in the itraconazole group (four with candidemia and one with Aspergillus pneumonia), and seven in the caspofungin group (two with candidemia, two with disseminated trichosporon species, two with Aspergillus pneumonia, and one with disseminated Fusarium spp). Two patients in the itraconazole group and four in the caspofungin group died of fungal infection (P = 0.57). Grade 3 to 4 adverse event rates were comparable between groups; the most common event in both was reversible hyperbilirubinemia. No evidence of cardiovascular toxicity from intravenous itraconazole was noted among patients older than 60. In conclusion, intravenous itraconazole and caspofungin provided similar protection against invasive fungal infection during induction chemotherapy, and both drugs were well tolerated.
引用
收藏
页码:143 / 147
页数:5
相关论文
共 24 条
  • [1] Congestive heart failure associated with itraconazole
    Ahmad, SR
    Singer, SJ
    Leissa, BG
    [J]. LANCET, 2001, 357 (9270) : 1766 - 1767
  • [2] [Anonymous], 2002, M27A2 CLIN LAB STAND
  • [3] [Anonymous], 1999, APPL SURVIVAL ANAL T
  • [4] Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: An international consensus
    Ascioglu, S
    Rex, JH
    de Pauw, B
    Bennett, JE
    Bille, J
    Crokaert, F
    Denning, DW
    Donnelly, JP
    Edwards, JE
    Erjavec, Z
    Fiere, D
    Lortholary, O
    Maertens, J
    Meis, JF
    Patterson, TF
    Ritter, J
    Selleslag, D
    Shah, PM
    Stevens, DA
    Walsh, TJ
    [J]. CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) : 7 - 14
  • [5] Becker R., 1988, The new S language
  • [6] COX DR, 1972, J R STAT SOC B, V34, P187
  • [7] Echinocandin antifungal drugs
    Denning, DW
    [J]. LANCET, 2003, 362 (9390) : 1142 - 1151
  • [8] Comparison of in vitro activities of the new triazole SCH56592 and the echinocandins MK-0991 (L-743,872) and LY303366 against opportunistic filamentous and dimorphic fungi and yeasts
    Espinel-Ingroff, A
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (10) : 2950 - 2956
  • [9] Itraconazole prevents invasive fungal infections in neutropenic patients treated for hematologic malignancies:: Evidence from a meta-analysis of 3,597 patients
    Glasmacher, A
    Prentice, A
    Gorschlüter, M
    Engelhart, S
    Hahn, C
    Djulbegovic, B
    Schmidt-Wolf, IGH
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) : 4615 - 4626
  • [10] Breakthrough trichosporonosis in a bone marrow transplant recipient receiving caspofungin acetate
    Goodman, D
    Pamer, E
    Jakubowski, A
    Morris, C
    Sepkowitz, K
    [J]. CLINICAL INFECTIOUS DISEASES, 2002, 35 (03) : E35 - E36