Cidofovir for adenovirus infections after allogeneic hematopoietic stem cell transplantation: a survey by the Infectious Diseases Working Party of the European Group for Blood and Marrow Transplantation

被引:185
作者
Ljungman, P [1 ]
Ribaud, P
Eyrich, M
Matthes-Martin, S
Einsele, H
Bleakley, M
Machaczka, M
Bierings, M
Bosi, A
Gratecos, N
Cordonnier, C
机构
[1] Huddinge Univ Hosp, Dept Hematol, Karolinska Inst, SE-14186 Stockholm, Sweden
[2] Hop St Louis, Paris, France
[3] Univ Tubingen Hosp, Tubingen, Germany
[4] St Anna Kinder Hosp, Vienna, Austria
[5] Univ Tubingen, Childrens Hosp, Tubingen, Germany
[6] New Childrens Hosp, Sydney, NSW, Australia
[7] Jagiellonian Univ, Krakow, Poland
[8] Univ Utrecht Hosp, Utrecht, Netherlands
[9] Univ Hosp, Florence, Italy
[10] Hop Archet, Nice, France
[11] Hop Henri Mondor, F-94010 Creteil, France
关键词
adenovirus; cidofovir; stem cell transplantation; allogeneic;
D O I
10.1038/sj.bmt.1703798
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Adenovirus is an important cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation and there is no established therapy. Cidofovir has in vitro efficacy against adenovirus. We performed a retrospective analysis of 45 patients treated with cidofovir for adenovirus from 10 centers. In total, 16 patients had definite adenovirus disease, 13 probable disease, and 16 asymptomatic infections. A total of 31 (69%) patients were successfully treated with cidofovir, 10 failed, and four were not evaluable owing to early death from other causes. Cidofovir therapy was successful in 10 patients with adenovirus disease, 10 patients with probable disease, and in 10 patients with asymptomatic infections. The overall survival at 28 days and 6 months after initiation of cidofovir therapy was 76 and 46%, respectively. Of the patients, 18 developed toxicity associated with cidofovir: 14 developed renal toxicity and four other types of toxicities. We conclude that cidofovir may be useful against adenovirus after allogeneic hematopoietic stem cell transplantation but additional studies are needed.
引用
收藏
页码:481 / 486
页数:6
相关论文
共 21 条
  • [1] Outcome and clinical course of 100 patients with adenovirus infection following bone marrow transplantation
    Baldwin, A
    Kingman, H
    Darville, M
    Foot, ABM
    Grier, D
    Cornish, JM
    Goulden, N
    Oakhill, A
    Pamphilon, DH
    Steward, CG
    Marks, DI
    [J]. BONE MARROW TRANSPLANTATION, 2000, 26 (12) : 1333 - 1338
  • [2] Bordigoni Pierre, 2001, Clinical Infectious Diseases, V32, P1290, DOI 10.1086/319984
  • [3] CASSANO WF, 1991, BONE MARROW TRANSPL, V7, P247
  • [4] Fulminant adenovirus hepatitis following unrelated bone marrow transplantation: failure of intravenous ribavirin therapy
    Chakrabarti, S
    Collingham, KE
    Fegan, CD
    Milligan, DW
    [J]. BONE MARROW TRANSPLANTATION, 1999, 23 (11) : 1209 - 1211
  • [5] De Clercq E, 1996, Verh K Acad Geneeskd Belg, V58, P19
  • [6] DECLERCQ E, 1996, VERH K ACAD GENEESKD, V58, P47
  • [7] Evaluation of Cidofovir (HPMPC, GS-504) against adenovirus type 5 infection in vitro and in a New Zealand rabbit ocular model
    deOliveira, CBR
    Stevenson, D
    LaBree, L
    McDonnell, PJ
    Trousdale, MD
    [J]. ANTIVIRAL RESEARCH, 1996, 31 (03) : 165 - 172
  • [8] INCREASING INCIDENCE OF ADENOVIRUS DISEASE IN BONE-MARROW TRANSPLANT RECIPIENTS
    FLOMENBERG, P
    BABBITT, J
    DROBYSKI, WR
    ASH, RC
    CARRIGAN, DR
    SEDMAK, GV
    MCAULIFFE, T
    CAMITTA, B
    HOROWITZ, MH
    BUNIN, N
    CASPER, JT
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (04) : 775 - 781
  • [9] Adenovirus infection after pediatric bone marrow transplantation
    Hale, GA
    Heslop, HE
    Krance, RA
    Brenner, MA
    Jayawardene, D
    Srivastava, DK
    Patrick, CC
    [J]. BONE MARROW TRANSPLANTATION, 1999, 23 (03) : 277 - 282
  • [10] Adenovirus infections in hematopoietic stem cell transplant recipients
    Howard, DS
    Phillips, GL
    Reece, DE
    Munn, RK
    Henslee-Downey, J
    Pittard, M
    Barker, M
    Pomeroy, C
    [J]. CLINICAL INFECTIOUS DISEASES, 1999, 29 (06) : 1494 - 1501