TY - JOUR
T1 - A prospective non-interventional study on the impact of transfusion burden and related iron toxicity on outcome in myelodysplastic syndromes undergoing allogeneic hematopoietic cell transplantation
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AU - Cremers, Eline M. P.
AU - de Witte, Theo
AU - de Wreede, Liesbeth
AU - Eikema, Diderik-Jan
AU - Koster, Linda
AU - van Biezen, Anja
AU - Finke, J. rgen
AU - Socié, Gerard
AU - Beelen, Dietrich
AU - Maertens, Johan
AU - Nagler, Arnon
AU - Kobbe, Guido
AU - Ziagkos, Dimitris
AU - Itälä-Remes, Maija
AU - Gedde-Dahl, Tobias
AU - Sierra, Jorge
AU - Niederwieser, Dietger
AU - Ljungman, Per
AU - Beguin, Yves
AU - Ozkurt, Zubeyde Nur
AU - Anagnostopoulos, Achilles
AU - Jindra, Pavel
AU - Robin, Marie
AU - Kröger, Nicolaus
PY - 2019/8/24
Y1 - 2019/8/24
N2 - Most myelodysplastic syndromes (MDS)-patients receive multiple red blood cell transfusions (RBCT). Transfusions may cause iron-related toxicity and mortality, influencing outcome after allogeneic HSCT. This prospective non-interventional study evaluated 222 MDS and CMML patients undergoing HSCT. Overall survival (OS), relapse-free survival (RFS), non-relapse mortality (NRM), and relapse incidence (RI) at 36 months were 52%, 44%, 25%, and 31%, respectively. Age, percentage of marrow blasts and severe comorbidities impacted OS. RFS was significantly associated with RBCT burden prior to HSCT (HR: 1.7; p =.02). High ferritin levels had a significant negative impact on OS and RI, but no impact on NRM. Administration of iron chelation therapy prior to HSCT did not influence the outcome, but early iron reduction after HSCT (started before 6 months) improved RFS significantly after transplantation (56% in the control group vs. 90% in the treated group, respectively; p =.04). This study illustrates the impact of RBCT and related parameters on HSCT-outcome. Patients with an expected prolonged survival after transplantation may benefit from early iron reduction therapy after transplantation.
AB - Most myelodysplastic syndromes (MDS)-patients receive multiple red blood cell transfusions (RBCT). Transfusions may cause iron-related toxicity and mortality, influencing outcome after allogeneic HSCT. This prospective non-interventional study evaluated 222 MDS and CMML patients undergoing HSCT. Overall survival (OS), relapse-free survival (RFS), non-relapse mortality (NRM), and relapse incidence (RI) at 36 months were 52%, 44%, 25%, and 31%, respectively. Age, percentage of marrow blasts and severe comorbidities impacted OS. RFS was significantly associated with RBCT burden prior to HSCT (HR: 1.7; p =.02). High ferritin levels had a significant negative impact on OS and RI, but no impact on NRM. Administration of iron chelation therapy prior to HSCT did not influence the outcome, but early iron reduction after HSCT (started before 6 months) improved RFS significantly after transplantation (56% in the control group vs. 90% in the treated group, respectively; p =.04). This study illustrates the impact of RBCT and related parameters on HSCT-outcome. Patients with an expected prolonged survival after transplantation may benefit from early iron reduction therapy after transplantation.
KW - MDS
KW - allogeneic stem cell transplantation
KW - chelation therapy
KW - phlebotomies
KW - transfusions
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064629113&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/30997844
U2 - 10.1080/10428194.2019.1594215
DO - 10.1080/10428194.2019.1594215
M3 - Article
C2 - 30997844
SN - 1042-8194
VL - 60
SP - 2404
EP - 2414
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 10
ER -