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

Hematology. 2010 Feb;15(1):4-10. doi: 10.1179/102453310X12583347009612.

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<0.001), donor seropositivity (P=0.002) and acute graft-versus-host disease (GVHD) (P=0.02) in the non-malignant subgroup and > or =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.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Bone Marrow Transplantation / adverse effects
  • Cord Blood Stem Cell Transplantation
  • Cytomegalovirus Infections / epidemiology*
  • Cytomegalovirus Infections / transmission
  • Disease Susceptibility
  • Female
  • Graft vs Host Disease / drug therapy
  • Graft vs Host Disease / epidemiology
  • Hematologic Diseases / complications
  • Hematologic Diseases / surgery*
  • Hematologic Neoplasms / complications
  • Hematologic Neoplasms / surgery*
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Humans
  • Immunocompromised Host
  • Immunosuppressive Agents / adverse effects
  • Immunosuppressive Agents / therapeutic use
  • Incidence
  • Living Donors
  • Male
  • Middle Aged
  • Opportunistic Infections / epidemiology*
  • Peripheral Blood Stem Cell Transplantation / adverse effects
  • Postoperative Complications / epidemiology*
  • Prospective Studies
  • Reoperation
  • Risk Factors
  • Transplantation, Homologous / adverse effects
  • Virus Activation
  • Young Adult

Substances

  • Immunosuppressive Agents