Early cytomegalovirus infections following allogeneic stem cell transplantation: a comparison between non-malignant and malignant haematological disorders

Md Serajul Islam*, Parameswaran Anoop, Phil Rice, Reuben Benjamin, Preeti Datta-Nemdharry, Edward C. Gordon-Smith, Judith Marsh

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)

    Abstract

    The haematological indications for allogeneic stem cell transplantation can be broadly divided into non-malignant and malignant disorders. We compared the incidence and risk factors for post-transplant cytomegalovirus (CMV) infections between these two biologically diverse subgroups of haematological conditions. Out of 105 allogeneic transplants, 64 and 41 were for underlying non-malignant and malignant indications respectively. CMV infections were significantly more frequent (P=0.016) in the malignant subgroup. Pre-transplant recipient CMV seropositivity in both subgroups (negative versus positive; non-malignant, P=0.023; malignant, p= 3 courses of previous cytotoxic therapy (P=0.023) in the malignant subgroup were found to be associated with an increased risk of CMV infections. On multivariate analysis, donor seropositivity in the non-malignant patients (negative versus positive, P=0.022; odds ratio: 0.18) and recipient seropositivity in patients with malignancies (negative versus positive; P=0.001, odds ratio: 0.01) were identified to be significant factors for risk of CMV infection.

    Original languageEnglish
    Pages (from-to)4-10
    Number of pages7
    JournalHEMATOLOGY
    Volume15
    Issue number1
    DOIs
    Publication statusPublished - Feb 2010

    Keywords

    • Cytomegalovirus
    • risk
    • transplantation
    • non-malignant
    • malignant
    • BONE-MARROW-TRANSPLANTATION
    • VERSUS-HOST-DISEASE
    • ACQUIRED APLASTIC-ANEMIA
    • ANTI-THYMOCYTE GLOBULIN
    • PERIPHERAL-BLOOD
    • IMMUNOSUPPRESSIVE THERAPY
    • UNRELATED DONORS
    • RISK-FACTORS
    • CORD BLOOD
    • REACTIVATION

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