Literature DB >> 16284613

Once daily ganciclovir as initial pre-emptive therapy delayed until threshold CMV load > or =10000 copies/ml: a safe and effective strategy for allogeneic stem cell transplant patients.

L A Verkruyse1, G A Storch, S M Devine, J F Dipersio, R Vij.   

Abstract

Quantitative polymerase chain reaction (QPCR) for cytomegalovirus (CMV) is emerging as the preferred screening method for detection of CMV viremia in patients following allogeneic bone marrow and peripheral blood stem cell transplant. However, there are currently no universally accepted QPCR treatment thresholds at which to start pre-emptive therapy. We report here results of a pre-emptive therapy strategy using ganciclovir (GCV) 5 mg/kg initiated once daily (ODG) delayed till a threshold CMV load of > or =10 000 copies/ml whole blood in clinically stable patients. Sixty-nine at risk patients underwent allogeneic stem cell transplant. 48/69 (70%) patients had an initial episode of CMV viremia. 5/48 (10%) cleared viremia without requiring treatment. 28/43 (65%) patients requiring treatment initiated treatment with ODG. 17/28 (61%) patients successfully cleared CMV viremia on ODG, 10/28 (36%) patients required dose escalation to twice daily GCV for increasing viral loads. There were two cases of CMV disease (colitis) and no deaths due to CMV disease in patients initiating treatment with ODG. We conclude delaying pre-emptive therapy with ODG until whole blood QPCR> or =10 000 copies/ml is a safe and effective strategy for CMV viremia after allogeneic stem cell transplant in clinically stable patients.

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Year:  2006        PMID: 16284613     DOI: 10.1038/sj.bmt.1705213

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  6 in total

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2.  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.

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Journal:  J Clin Microbiol       Date:  2008-08-27       Impact factor: 5.948

3.  Mobilization of allogeneic peripheral blood stem cell donors with intravenous plerixafor mobilizes a unique graft.

Authors:  Mark A Schroeder; Michael P Rettig; Sandra Lopez; Stephanie Christ; Mark Fiala; William Eades; Fazia A Mir; Jin Shao; Kyle McFarland; Kathryn Trinkaus; William Shannon; Elena Deych; Jinsheng Yu; Ravi Vij; Keith Stockerl-Goldstein; Amanda F Cashen; Geoffrey L Uy; Camille N Abboud; Peter Westervelt; John F DiPersio
Journal:  Blood       Date:  2017-03-14       Impact factor: 22.113

4.  Overview of the diagnosis of cytomegalovirus infection.

Authors:  S A Ross; Z Novak; S Pati; S B Boppana
Journal:  Infect Disord Drug Targets       Date:  2011-10

5.  Investigation of Cytomegalovirus in Intestinal Tissue in a Country With High CMV Seroprevalence.

Authors:  Hande Hazır-Konya; Vildan Avkan-Oğuz; Hale Akpınar; Özgül Sağol; Arzu Sayıner
Journal:  Turk J Gastroenterol       Date:  2021-02       Impact factor: 1.852

6.  Comparison of quantitative cytomegalovirus real-time PCR in whole blood and pp65 antigenemia assay: clinical utility of CMV real-time PCR in hematopoietic stem cell transplant recipients.

Authors:  Su-Mi Choi; Dong-Gun Lee; Jihyang Lim; Sun Hee Park; Jung-Hyun Choi; Jin-Hong Yoo; Jong-Wook Lee; Yonggoo Kim; Kyungja Han; Woo-Sung Min; Wan-Shik Shin; Chun-Choo Kim
Journal:  J Korean Med Sci       Date:  2009-07-29       Impact factor: 2.153

  6 in total

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