TY - JOUR
T1 - Late treatment-related mortality versus competing causes of death after allogeneic transplantation for myelodysplastic syndromes and secondary acute myeloid leukemia
AU - Schetelig, Johannes
AU - de Wreede, Liesbeth C.
AU - van Gelder, Michel
AU - Koster, Linda
AU - Finke, Jürgen
AU - Niederwieser, Dietger
AU - Beelen, Dietrich
AU - Mufti, G. J.
AU - Platzbecker, Uwe
AU - Ganser, Arnold
AU - Heidenreich, Silke
AU - Maertens, Johan
AU - Socié, Gerard
AU - Brecht, Arne
AU - Stelljes, Matthias
AU - Kobbe, Guido
AU - Volin, Liisa
AU - Nagler, Arnon
AU - Vitek, Antonin
AU - Luft, Thomas
AU - Ljungman, Per
AU - Yakoub-Agha, Ibrahim
AU - Robin, Marie
AU - Kröger, Nicolaus
PY - 2019/3/1
Y1 - 2019/3/1
N2 - The causes and rates of late patient-mortality following alloHCT for myelodysplastic syndromes or secondary acute myeloid leukemia were studied, to assess the contribution of relapse-related, treatment-related, and population factors. Data from EBMT on 6434 adults, who received a first alloHCT from January 2000 to December 2012, were retrospectively studied using combined land-marking, relative-survival methods and multi-state modeling techniques. Median age at alloHCT increased from 49 to 58 years, and the number of patients aged ≥65 years at alloHCT increased from 5 to 17%. Overall survival probability was 53% at 2 years and 35% at 10 years post-alloHCT. Survival probability at 5 years from the 2-year landmark was 88% for patients <45-year old and 63% for patients ≥65-year old at alloHCT. Cumulative incidence of nonrelapse mortality (NRM) for patients <45-year old at transplant was 7% rising to 25% for patients aged ≥65. For older patients, 31% of NRM-deaths could be attributed to population mortality. Favorable post-alloHCT long-term survival was seen; however, excess mortality-risk for all age groups was shown compared to the general population. A substantial part of total NRM for older patients was attributable to population mortality, information which aids the balanced explanation of post-HCT risk and helps improve long-term care.
AB - The causes and rates of late patient-mortality following alloHCT for myelodysplastic syndromes or secondary acute myeloid leukemia were studied, to assess the contribution of relapse-related, treatment-related, and population factors. Data from EBMT on 6434 adults, who received a first alloHCT from January 2000 to December 2012, were retrospectively studied using combined land-marking, relative-survival methods and multi-state modeling techniques. Median age at alloHCT increased from 49 to 58 years, and the number of patients aged ≥65 years at alloHCT increased from 5 to 17%. Overall survival probability was 53% at 2 years and 35% at 10 years post-alloHCT. Survival probability at 5 years from the 2-year landmark was 88% for patients <45-year old and 63% for patients ≥65-year old at alloHCT. Cumulative incidence of nonrelapse mortality (NRM) for patients <45-year old at transplant was 7% rising to 25% for patients aged ≥65. For older patients, 31% of NRM-deaths could be attributed to population mortality. Favorable post-alloHCT long-term survival was seen; however, excess mortality-risk for all age groups was shown compared to the general population. A substantial part of total NRM for older patients was attributable to population mortality, information which aids the balanced explanation of post-HCT risk and helps improve long-term care.
UR - http://www.scopus.com/inward/record.url?scp=85058928766&partnerID=8YFLogxK
U2 - 10.1038/s41375-018-0302-y
DO - 10.1038/s41375-018-0302-y
M3 - Article
C2 - 30573777
AN - SCOPUS:85058928766
SN - 0887-6924
VL - 33
SP - 686
EP - 695
JO - Leukemia
JF - Leukemia
IS - 3
ER -