CMV reactivation after allogeneic HCT and relapse risk: evidence for early protection in acute myeloid leukemia

Blood. 2013 Aug 15;122(7):1316-24. doi: 10.1182/blood-2013-02-487074. Epub 2013 Jun 6.

Abstract

The association between cytomegalovirus (CMV) reactivation and relapse was evaluated in a large cohort of patients with acute myeloid leukemia (AML) (n = 761), acute lymphoblastic leukemia (ALL) (n = 322), chronic myeloid leukemia (CML) (n = 646), lymphoma (n = 254), and myelodysplastic syndrome (MDS) (n = 371) who underwent allogeneic hematopoietic cell transplantation (HCT) between 1995 and 2005. In multivariable models, CMV pp65 antigenemia was associated with a decreased risk of relapse by day 100 among patients with AML (hazard ratio [HR] = 0.56; 95% confidence interval [CI], 0.3-0.9) but not in patients with ALL, lymphoma, CML, or MDS. The effect appeared to be independent of CMV viral load, acute graft-versus-host disease, or ganciclovir-associated neutropenia. At 1 year after HCT, early CMV reactivation was associated with reduced risk of relapse in all patients, but this did not reach significance for any disease subgroup. Furthermore, CMV reactivation was associated with increased nonrelapse mortality (HR = 1.31; 95% CI, 1.1-1.6) and no difference in overall mortality (HR = 1.05; 95% CI, 0.9-1.3). This report demonstrates a modest reduction in early relapse risk after HCT associated with CMV reactivation in a large cohort of patients without a benefit in overall survival.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Cytomegalovirus / physiology*
  • Cytomegalovirus Infections / etiology
  • Cytomegalovirus Infections / mortality
  • Cytomegalovirus Infections / prevention & control*
  • Female
  • Follow-Up Studies
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / mortality
  • Graft vs Host Disease / prevention & control
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Infant
  • Infant, Newborn
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / complications
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / prevention & control
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / virology
  • Leukemia, Myeloid, Acute / complications
  • Leukemia, Myeloid, Acute / prevention & control*
  • Leukemia, Myeloid, Acute / virology
  • Lymphoma / complications
  • Lymphoma / prevention & control
  • Lymphoma / virology
  • Male
  • Myelodysplastic Syndromes / complications
  • Myelodysplastic Syndromes / prevention & control
  • Myelodysplastic Syndromes / virology
  • Neoplasm Recurrence, Local / mortality
  • Neoplasm Recurrence, Local / prevention & control*
  • Neoplasm Recurrence, Local / virology
  • Phosphoproteins / blood
  • Phosphoproteins / immunology*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / complications
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / prevention & control
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / virology
  • Prognosis
  • Retrospective Studies
  • Risk Factors
  • Survival Rate
  • Transplantation Conditioning
  • Transplantation, Homologous
  • Viral Matrix Proteins / blood
  • Viral Matrix Proteins / immunology*
  • Virus Activation*
  • Young Adult

Substances

  • Phosphoproteins
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa