Efficacy of a Viral Load-Based, Risk-Adapted, Preemptive Treatment Strategy for Prevention of Cytomegalovirus Disease after Hematopoietic Cell Transplantation

被引:126
作者
Green, Margaret L. [1 ,2 ]
Leisenring, Wendy [3 ]
Stachel, Daniel [6 ]
Pergam, Steven A. [2 ]
Sandmaier, Brenda M. [2 ]
Wald, Anna [2 ,4 ,5 ]
Corey, Lawrence [2 ,4 ]
Boeckh, Michael [2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
[2] Univ Washington, Dept Med, Seattle, WA USA
[3] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[4] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[5] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[6] Univ Erlangen Nurnberg, D-91054 Erlangen, Germany
基金
美国国家卫生研究院;
关键词
Cytomegalovirus; PCR; Preemptive therapy; Hematopoietic cell transplantation; ALLOGENEIC MARROW TRANSPLANTATION; POLYMERASE-CHAIN-REACTION; PP65; ANTIGENEMIA; FUNGAL-INFECTIONS; DNAEMIA CUTOFF; DOUBLE-BLIND; RECIPIENTS; PLASMA; PROPHYLAXIS; DNA;
D O I
10.1016/j.bbmt.2012.05.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytomegalovirus (CMV) surveillance and preemptive therapy is the most commonly used strategy for CMV disease prevention in hematopoietic cell transplantation recipients. In 2007, we introduced a CMV prevention strategy for patients at risk for CMV disease using quantitative PCR surveillance, with treatment thresholds determined by patient risk factors. Patients (N = 367) received preemptive therapy either at a plasma viral load of >= 500 copies/mL, at >= 100 copies/mL if receiving >= 1 mg/kg of prednisone or anti-T cell therapies, or if a >= 5-fold viral load increase from baseline was detected. Compared with patients before 2007 undergoing antigenemia-based surveillance (n = 690) with preemptive therapy initiated for any positive level, the risk-adapted PCR-based strategy resulted in similar use of antiviral agents, and similar risks of CMV disease, toxicity, and nonrelapse mortality in multivariable models. The cumulative incidence of CMV disease by day 100 was 5.2% in the PCR group compared with 5.8% in the antigenemia group ( I year: 9.1% PCR vs 9.6% antigenennia). Breakthrough CMV disease in the PCR group was predominantly in the gastrointestinal (GI) tract (15 of 19 cases; 79%). However, unlike CMV pneumonia, CMV GI disease was not associated with increased nonrelapse mortality (adjusted hazard ratio, 1.19; P = .70 [GI disease] vs 8.18; P < .001 [pneumonia]). Thus, the transition to a preemptive therapy strategy based on CMV viral load and host risk factors successfully prevented CMV disease without increasing the proportion of patients receiving preemptive therapy and attributable toxicity. Breakthrough disease in PCR-based preemptive therapy occurs at a low incidence and presents primarily as GI disease, which is more likely to be responsive to antiviral therapy. Biol Blood Marrow Transplant 18: 1687-1699 (2012) (C) 2012 American Sock?), for Blood and Marrow Transplantation
引用
收藏
页码:1687 / 1699
页数:13
相关论文
共 42 条
  • [1] Optimization of quantitative detection of cytomegalovirus DNA in plasma by real-time PCR
    Boeckh, M
    Huang, M
    Ferrenberg, J
    Stevens-Ayers, T
    Stensland, L
    Nichols, WG
    Corey, L
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (03) : 1142 - 1148
  • [2] The impact of cytomegalovirus serostatus of donor and recipient before hematopoietic stem cell transplantation in the era of antiviral prophylaxis and preemptive therapy
    Boeckh, M
    Nichols, WG
    [J]. BLOOD, 2004, 103 (06) : 2003 - 2008
  • [3] Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity
    Boeckh, M
    Leisenring, W
    Riddell, SR
    Bowden, RA
    Huang, ML
    Myerson, D
    Stevens-Ayers, T
    Flowers, MED
    Cunningham, T
    Corey, L
    [J]. BLOOD, 2003, 101 (02) : 407 - 414
  • [4] Successful modification of a pp65 antigenemia-based early treatment strategy for prevention of cytomegalovirus disease in allogeneic marrow transplant recipients
    Boeckh, M
    Bowden, RA
    Gooley, T
    Myerson, D
    Corey, L
    [J]. BLOOD, 1999, 93 (05) : 1781 - 1782
  • [5] Plasma polymerase chain reaction for cytomegalovirus DNA after allogeneic marrow transplantation - Comparison with polymerase chain reaction using peripheral blood leukocytes, pp65 antigenemia, and viral culture
    Boeckh, M
    GallezHawkins, GM
    Myerson, D
    Zaia, JA
    Bowden, RA
    [J]. TRANSPLANTATION, 1997, 64 (01) : 108 - 113
  • [6] Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study
    Boeckh, M
    Gooley, TA
    Myerson, D
    Cunningham, T
    Schoch, G
    Bowden, RA
    [J]. BLOOD, 1996, 88 (10) : 4063 - 4071
  • [7] Comparative Evaluation of Three Automated Systems for DNA Extraction in Conjunction with Three Commercially Available Real-Time PCR Assays for Quantitation of Plasma Cytomegalovirus DNAemia in Allogeneic Stem Cell Transplant Recipients
    Bravo, Dayana
    Angeles Clari, Maria
    Costa, Elisa
    Munoz-Cobo, Beatriz
    Solano, Carlos
    Jose Remigia, Maria
    Navarro, David
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (08) : 2899 - 2904
  • [8] Lipopolysaccharide binding protein promoter variants influence the risk for Gram-negative bacteremia and mortality after allogeneic hematopoietic cell transplantation
    Chien, Jason W.
    Boeckh, Michael J.
    Hansen, John A.
    Clark, Joan G.
    [J]. BLOOD, 2008, 111 (04) : 2462 - 2469
  • [9] Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group
    De Pauw, Ben
    Walsh, Thomas J.
    Donnelly, J. Peter
    Stevens, David A.
    Edwards, John E.
    Calandra, Thierry
    Pappas, Peter G.
    Maertens, Johan
    Lortholary, Olivier
    Kauffman, Carol A.
    Denning, David W.
    Patterson, Thomas F.
    Maschmeyer, Georg
    Bille, Jacques
    Dismukes, William E.
    Herbrecht, Raoul
    Hope, William W.
    Kibbler, Christopher C.
    Kullberg, Bart Jan
    Marr, Kieren A.
    Munoz, Patricia
    Odds, Frank C.
    Perfect, John R.
    Restrepo, Angela
    Ruhnke, Markus
    Segal, Brahm H.
    Sobel, Jack D.
    Sorrell, Tania C.
    Viscoli, Claudio
    Wingard, John R.
    Zaoutis, Theoklis
    Bennett, John E.
    [J]. CLINICAL INFECTIOUS DISEASES, 2008, 46 (12) : 1813 - 1821
  • [10] Risk factors for treatment failures in patients receiving PCR-based preemptive therapy for CMV infection
    Einsele, H
    Hebart, H
    Kauffman-Schneider, C
    Sinzger, C
    Jahn, G
    Bader, P
    Klingebiel, T
    Dietz, K
    Löffler, J
    Bokemeyer, C
    Müller, CA
    Kanz, L
    [J]. BONE MARROW TRANSPLANTATION, 2000, 25 (07) : 757 - 763