Posaconazole vs. fluconazole or itraconazole prophylaxis in patients with neutropenia

被引:1304
作者
Cornely, Oliver A.
Maertens, Johan
Winston, Drew J.
Perfect, John
Ullmann, Andrew J.
Walsh, Thomas J.
Helfgott, David
Holowiecki, Jerzy
Stockelberg, Dick
Goh, Yeow-Tee
Petrini, Mario
Hardalo, Cathy
Suresh, Ramachandran
Angulo-Gonzalez, David
机构
[1] Univ Cologne, Cologne, Germany
[2] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
[3] Univ Calif Los Angeles, Los Angeles, CA USA
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Johannes Gutenberg Univ Mainz, D-6500 Mainz, Germany
[6] NCI, Bethesda, MD 20892 USA
[7] Weill Cornell Med Coll, New York, NY USA
[8] Silesian Med Univ, Katowice, Poland
[9] Sahlgrens Univ Hosp, Gothenburg, Sweden
[10] Singapore Gen Hosp, Singapore 0316, Singapore
[11] Univ Pisa, Pisa, Italy
[12] Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA
关键词
D O I
10.1056/NEJMoa061094
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Patients with neutropenia resulting from chemotherapy for acute myelogenous leukemia or the myelodysplastic syndrome are at high risk for difficult-to-treat and often fatal invasive fungal infections. METHODS: In this randomized, multicenter study involving evaluators who were unaware of treatment assignments, we compared the efficacy and safety of posaconazole with those of fluconazole or itraconazole as prophylaxis for patients with prolonged neutropenia. Patients received prophylaxis with each cycle of chemotherapy until recovery from neutropenia and complete remission, until occurrence of an invasive fungal infection, or for up to 12 weeks, whichever came first. We compared the incidence of proven or probable invasive fungal infections during treatment (the primary end point) between the posaconazole and fluconazole or itraconazole groups; death from any cause and time to death were secondary end points. RESULTS: A total of 304 patients were randomly assigned to receive posaconazole, and 298 patients were randomly assigned to receive fluconazole (240) or itraconazole (58). Proven or probable invasive fungal infections were reported in 7 patients (2%) in the posaconazole group and 25 patients (8%) in the fluconazole or itraconazole group (absolute reduction in the posaconazole group, -6%; 95% confidence interval, -9.7 to -2.5%; P<0.001), fulfilling statistical criteria for superiority. Significantly fewer patients in the posaconazole group had invasive aspergillosis (2 [1%] vs. 20 [7%], P<0.001). Survival was significantly longer among recipients of posaconazole than among recipients of fluconazole or itraconazole (P=0.04). Serious adverse events possibly or probably related to treatment were reported by 19 patients (6%) in the posaconazole group and 6 patients (2%) in the fluconazole or itraconazole group (P=0.01). The most common treatment-related adverse events in both groups were gastrointestinal tract disturbances. CONCLUSIONS: In patients undergoing chemotherapy for acute myelogenous leukemia or the myelodysplastic syndrome, posaconazole prevented invasive fungal infections more effectively than did either fluconazole or itraconazole and improved overall survival. There were more serious adverse events possibly or probably related to treatment in the posaconazole group.
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页码:348 / 359
页数:12
相关论文
共 38 条
  • [1] [Anonymous], 2002, M27A2 CLSI
  • [2] 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
  • [3] Fusarium, a significant emerging pathogen in patients with hematologic malignancy: Ten years' experience at a cancer center and implications for management
    Boutati, EI
    Anaissie, EJ
    [J]. BLOOD, 1997, 90 (03) : 999 - 1008
  • [4] INVASIVE FUNGAL DISEASE IN ADULTS UNDERGOING REMISSION-INDUCTION THERAPY FOR ACUTE MYELOID-LEUKEMIA - THE PATHOGENETIC ROLE OF THE ANTILEUKEMIC REGIMEN
    BOW, EJ
    LOEWEN, R
    CHEANG, MS
    SCHACTER, B
    [J]. CLINICAL INFECTIOUS DISEASES, 1995, 21 (02) : 361 - 369
  • [5] Rapid method for the analysis of itraconazole and hydroxyitraconazole in serum by high-performance liquid chromatography
    Compas, D
    Touw, DJ
    deGoede, PNFC
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1996, 687 (02): : 453 - 456
  • [6] COOK RJ, 1995, BRIT MED J, V310, P1056
  • [7] Evidence-based assessment of primary antifungal prophylaxis in patients with hematologic malignancies
    Cornely, OA
    Ullmann, AJ
    Karthaus, M
    [J]. BLOOD, 2003, 101 (09) : 3365 - 3372
  • [8] An EORTC multicentre prospective survey of invasive aspergillosis in haematological patients: Diagnosis and therapeutic outcome
    Denning, DW
    Marinus, A
    Cohen, J
    Spence, D
    Herbrecht, R
    Pagano, L
    Kibbler, C
    Kcrmery, V
    Offner, F
    Cordonnier, C
    Jehn, U
    Ellis, M
    Collette, L
    Sylvester, R
    [J]. JOURNAL OF INFECTION, 1998, 37 (02) : 173 - 180
  • [9] An open-label randomized trial comparing itraconazole oral solution with fluconazole oral solution for primary prophylaxis of fungal infections in patients with haematological malignancy and profound neutropenia
    Glasmacher, A
    Cornely, O
    Ullmann, AJ
    Wedding, U
    Bodenstein, H
    Wandt, H
    Boewer, C
    Pasold, R
    Wolf, HH
    Hänel, M
    Dölken, G
    Junghanss, C
    Andreesen, R
    Bertz, H
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (02) : 317 - 325
  • [10] 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