Death after hematopoietic stem cell transplantation: changes over calendar year time, infections and associated factors
- Creators
- Styczynski J.
- Tridello G.
- Koster L.
- Iacobelli S.
- van Biezen A.
- van der Werf S.
- Mikulska M.
- Gil L.
- Cordonnier C.
- Ljungman P.
- Averbuch D.
- Cesaro S.
- de la Camara R.
- Baldomero H.
- Bader P.
- Basak G.
- Bonini C.
- Duarte R.
- Dufour C.
- Kuball J.
- Lankester A.
- Montoto S.
- Nagler A.
- Snowden J. A.
- Kroger N.
- Mohty M.
- Gratwohl A.
- Others:
- Styczynski, J.
- Tridello, G.
- Koster, L.
- Iacobelli, S.
- van Biezen, A.
- van der Werf, S.
- Mikulska, M.
- Gil, L.
- Cordonnier, C.
- Ljungman, P.
- Averbuch, D.
- Cesaro, S.
- de la Camara, R.
- Baldomero, H.
- Bader, P.
- Basak, G.
- Bonini, C.
- Duarte, R.
- Dufour, C.
- Kuball, J.
- Lankester, A.
- Montoto, S.
- Nagler, A.
- Snowden, J. A.
- Kroger, N.
- Mohty, M.
- Gratwohl, A.
Description
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".
Additional details
- URL
- http://hdl.handle.net/11567/1037446
- URN
- urn:oai:iris.unige.it:11567/1037446
- Origin repository
- UNIGE