Death after hematopoietic stem cell transplantation: changes over calendar year time, infections and associated factors

  • Jan Styczyński
  • Gloria Tridello
  • Linda Koster
  • Simona Iacobelli
  • Anja van Biezen
  • Steffie van der Werf
  • Małgorzata Mikulska
  • Lidia Gil
  • Catherine Cordonnier
  • Per Ljungman
  • Diana Averbuch
  • Simone Cesaro
  • Rafael de la Camara
  • Helen Baldomero
  • Peter Bader
  • Grzegorz Basak
  • Chiara Bonini
  • Rafael Duarte
  • Carlo Dufour
  • Jurgen Kuball
  • Arjan Lankester
  • Silvia Montoto
  • Arnon Nagler
  • John A Snowden
  • Nicolaus Kröger
  • Mohamad Mohty
  • Alois Gratwohl
  • Infectious Diseases Working Party EBMT

Abstract

Information on incidence, and factors associated with mortality is a prerequisite to improve outcome after hematopoietic stem cell transplantation (HSCT). Therefore, 55'668 deaths in 114'491 patients with HSCT (83.7% allogeneic) for leukemia were investigated in a landmark analysis for causes of death at day 30 (very early), day 100 (early), at 1 year (intermediate) and at 5 years (late). Mortality from all causes decreased from cohort 1 (1980-2001) to cohort 2 (2002-2015) in all post-transplant phases after autologous HSCT. After allogeneic HSCT, mortality from infections, GVHD, and toxicity decreased up to 1 year, increased at 5 years; deaths from relapse increased in all post-transplant phases. Infections of unknown origin were the main cause of infectious deaths. Lethal bacterial and fungal infections decreased from cohort 1 to cohort 2, not unknown or mixed infections. Infectious deaths were associated with patient-, disease-, donor type, stem cell source, center, and country- related factors. Their impact varied over the post-transplant phases. Transplant centres have successfully managed to reduce death after HSCT in the early and intermediate post-transplant phases, and have identified risk factors. Late post-transplant care could be improved by focus on groups at risk and better identification of infections of "unknown origin".

Bibliographical data

Original languageEnglish
ISSN0268-3369
DOIs
Publication statusPublished - 01.2020
PubMed 31455899