Literature DB >> 11682510

Qualitative plasma PCR assay (AMPLICOR CMV test) versus pp65 antigenemia assay for monitoring cytomegalovirus viremia and guiding preemptive ganciclovir therapy in allogeneic stem cell transplantation.

C Solano1, I Muñoz, A Gutiérrez, A Farga, F Prósper, J García-Conde, D Navarro, C Gimeno.   

Abstract

The performances of a commercially available qualitative plasma PCR assay (AMPLICOR CMV test; Roche Diagnostics) and the pp65 antigenemia assay (AG) were evaluated for the monitoring of cytomegalovirus (CMV) viremia in 43 allogeneic stem cell transplant recipients. In addition, the suitabilities of both assays for triggering the initiation of preemptive ganciclovir therapy were assessed. A total of 37 CMV viremic episodes were detected in 28 patients. Positivity of plasma PCR testing in one or more consecutive specimens was the only marker of CMV viremia in 18 of the 37 episodes (PCR positive and AG negative, n = 50 specimens). Five episodes were diagnosed on the basis of a single positive AG result (AG positive and PCR negative, n = 5 specimens); both assays were eventually positive (PCR positive and AG positive, n = 27 specimens) for 14 viremic episodes; for these episodes, conversion of the PCR assay result to a positive result occurred an average of 1 week before conversion of the AG result. Overall, the concordance between the two methods was 90%, and the sensitivities of the plasma PCR assay and AG for the detection of CMV viremic episodes were 86.5 and 51.3%, respectively. Two patients who tested positive by both assays simultaneously progressed to CMV end-stage organ disease, despite the initiation of preemptive ganciclovir therapy. Conversion of the AG result to a negative result upon administration of preemptive ganciclovir therapy occurred a median of 7.5 days earlier than conversion of the plasma PCR assay result. Nineteen of the 28 patients with CMV viremia received AG-guided preemptive ganciclovir therapy; had the positivity of the plasma PCR assay triggered the initiation of preemptive therapy, 9 additional patients would have been unnecessarily treated since none of them developed CMV end-stage organ disease. Although the AMPLICOR CMV assay is more sensitive than AG, the latter appears to be more suitable both for guiding the initiation of preemptive therapy and for monitoring a patient's response to antiviral therapy.

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Year:  2001        PMID: 11682510      PMCID: PMC88467          DOI: 10.1128/JCM.39.11.3938-3941.2001

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  27 in total

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Authors:  A Weinberg; T N Hodges; S Li; G Cai; M R Zamora
Journal:  J Clin Microbiol       Date:  2000-02       Impact factor: 5.948

2.  Successful modification of a pp65 antigenemia-based early treatment strategy for prevention of cytomegalovirus disease in allogeneic marrow transplant recipients.

Authors:  M Boeckh; R A Bowden; T Gooley; D Myerson; L Corey
Journal:  Blood       Date:  1999-03-01       Impact factor: 22.113

3.  Real-time automated PCR for early diagnosis and monitoring of cytomegalovirus infection after bone marrow transplantation.

Authors:  U Machida; M Kami; T Fukui; Y Kazuyama; M Kinoshita; Y Tanaka; Y Kanda; S Ogawa; H Honda; S Chiba; K Mitani; Y Muto; K Osumi; S Kimura; H Hirai
Journal:  J Clin Microbiol       Date:  2000-07       Impact factor: 5.948

4.  Comparison of quantitative cytomegalovirus (CMV) PCR in plasma and CMV antigenemia assay: clinical utility of the prototype AMPLICOR CMV MONITOR test in transplant recipients.

Authors:  A M Caliendo; K St George; S Y Kao; J Allega; B H Tan; R LaFontaine; L Bui; C R Rinaldo
Journal:  J Clin Microbiol       Date:  2000-06       Impact factor: 5.948

5.  Risk-adapted pre-emptive therapy for cytomegalovirus disease in patients undergoing allogeneic bone marrow transplantation.

Authors:  T Mori; S Okamoto; S Matsuoka; T Yajima; M Wakui; R Watanabe; A Ishida; Y Iwao; M Mukai; T Hibi; Y Ikeda
Journal:  Bone Marrow Transplant       Date:  2000-04       Impact factor: 5.483

6.  Quantitative analysis of cytomegalovirus (CMV) viremia using the pp65 antigenemia assay and the COBAS AMPLICOR CMV MONITOR PCR test after blood and marrow allogeneic transplantation.

Authors:  G Boivin; R Bélanger; R Delage; C Béliveau; C Demers; N Goyette; J Roy
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

7.  Evaluation of diagnostic methods for the detection of cytomegalovirus in recipients of allogeneic stem cell transplants.

Authors:  W Preiser; S Bräuninger; R Schwerdtfeger; U Ayliffe; J A Garson; N S Brink; S Franck; H W Doerr; H F Rabenau
Journal:  J Clin Virol       Date:  2001-01       Impact factor: 3.168

8.  Human cytomegalovirus immediate-early mRNA detection by nucleic acid sequence-based amplification as a new parameter for preemptive therapy in bone marrow transplant recipients.

Authors:  G Gerna; F Baldanti; D Lilleri; M Parea; E Alessandrino; A Pagani; F Locatelli; J Middeldorp; M G Revello
Journal:  J Clin Microbiol       Date:  2000-05       Impact factor: 5.948

9.  A randomized, controlled trial of prophylactic ganciclovir for cytomegalovirus pulmonary infection in recipients of allogeneic bone marrow transplants; The City of Hope-Stanford-Syntex CMV Study Group.

Authors:  G M Schmidt; D A Horak; J C Niland; S R Duncan; S J Forman; J A Zaia
Journal:  N Engl J Med       Date:  1991-04-11       Impact factor: 91.245

10.  Early treatment with ganciclovir to prevent cytomegalovirus disease after allogeneic bone marrow transplantation.

Authors:  J M Goodrich; M Mori; C A Gleaves; C Du Mond; M Cays; D F Ebeling; W C Buhles; B DeArmond; J D Meyers
Journal:  N Engl J Med       Date:  1991-12-05       Impact factor: 91.245

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  8 in total

1.  Quantification of DNA in plasma by an automated real-time PCR assay (cytomegalovirus PCR kit) for surveillance of active cytomegalovirus infection and guidance of preemptive therapy for allogeneic hematopoietic stem cell transplant recipients.

Authors:  Concepción Gimeno; Carlos Solano; José C Latorre; Juan C Hernández-Boluda; María A Clari; María J Remigia; Santiago Furió; Marisa Calabuig; Nuria Tormo; David Navarro
Journal:  J Clin Microbiol       Date:  2008-08-27       Impact factor: 5.948

2.  Improved monitoring of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation by an ultrasensitive plasma DNA PCR assay.

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Journal:  J Clin Microbiol       Date:  2002-11       Impact factor: 5.948

3.  Impact of hospital length of stay on the risk of readmission and overall survival after allogeneic stem cell transplantation.

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Review 4.  Prevention of cytomegalovirus disease in recipients of allogeneic stem cell transplants.

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5.  Monitoring of cytomegalovirus reactivation in bone marrow transplant recipients by real-time PCR.

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6.  A prospective study comparing quantitative Cytomegalovirus (CMV) polymerase chain reaction in plasma and pp65 antigenemia assay in monitoring patients after allogeneic stem cell transplantation.

Authors:  Giuseppe Gentile; Alessandra Picardi; Angela Capobianchi; Alessandra Spagnoli; Laura Cudillo; Teresa Dentamaro; Andrea Tendas; Luca Cupelli; Marco Ciotti; Antonio Volpi; Sergio Amadori; Pietro Martino; Paolo de Fabritiis
Journal:  BMC Infect Dis       Date:  2006-11-21       Impact factor: 3.090

7.  Comparison of the Commercial QuantiFERON-CMV and Overlapping Peptide-based ELISPOT Assays for Predicting CMV Infection in Kidney Transplant Recipients.

Authors:  Ji-Soo Kwon; Taeeun Kim; Sun-Mi Kim; Heungsup Sung; Sung Shin; Young Hoon Kim; Eui-Cheol Shin; Sung-Han Kim; Duck Jong Han
Journal:  Immune Netw       Date:  2017-10-25       Impact factor: 6.303

8.  Factors associated with cytomegalovirus infection in children undergoing allogeneic hematopoietic stem-cell transplantation.

Authors:  Tang-Her Jaing; Tsung-Yen Chang; Shih-Hsiang Chen; Yu-Chuan Wen; Ting-Jiuan Yu; Ching-Fen Lee; Chao-Ping Yang; Pei-Kwei Tsay
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  8 in total

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