Reduction of infection-related mortality after allogeneic PBSCT from HLA-identical siblings: Longitudinal analysis from 1994 to 2008 at a single institution

R. Martino, A. Kerguelen, D. Valcárcel, A. Sureda, L. Fachini, J. L. Piñana, J. Briones, J. Delgado, S. Brunet, J. Sierra

Research output: Contribution to journalArticleResearchpeer-review

20 Citations (Scopus)

Abstract

Infection-related mortality (IRM) is responsible for a major proportion of all cases of non-relapse mortality (NRM) after allogeneic PBSCT (alloPBSCT). We analyzed 580 consecutive adults who received a first alloPBSCT from an HLA-identical sibling from 1994 to 2008 at a single institution to describe the severe infections and report the incidence, causes and risk factors for IRM and NRM. Both IRM and NRM decreased with time; within the period of 1994-2000, the 2-year incidence of IRM and NRM was 22 and 31%, respectively, vs 11 and 16% within the period of 2001-2008 (P<0.05 for both comparisons). In multivariate analysis, the variables that increased IRM were within the earlier period of 1994-2000 (P<0.01), poor performance status (P<0.01), grade II-IV acute GVHD (P<0.001) and invasive fungal infection (IFI) (P<0.001) or CMV disease (P<0.001) after transplant. With respect to NRM, earlier time period was also identified as a risk factor (P<0.001), as well as IFIs (P<0.001) and CMV disease (P<0.001). The intensity of the conditioning regimen had no effect on IRM and NRM. These results showed a significant reduction in IRM and NRM over a period of 15 years. The development of IFIs and CMV disease continue to have an impact on NRM. © 2011 Macmillan Publishers Limited All rights reserved.
Original languageEnglish
Pages (from-to)690-701
JournalBone Marrow Transplantation
Volume46
Issue number5
DOIs
Publication statusPublished - 1 May 2011

Keywords

  • allogeneic
  • infections
  • PBSCT

Fingerprint

Dive into the research topics of 'Reduction of infection-related mortality after allogeneic PBSCT from HLA-identical siblings: Longitudinal analysis from 1994 to 2008 at a single institution'. Together they form a unique fingerprint.

Cite this