TY - JOUR
T1 - Impact of treatment with iron chelation therapy in patients with lower-risk myelodysplastic syndromes participating in the European MDS registry
AU - EUMDS Registry Participants
AU - Hoeks, Marlijn
AU - Yu, Ge
AU - Langemeijer, Saskia
AU - Crouch, Simon
AU - de Swart, Louise
AU - Fenaux, Pierre
AU - Symeonidis, Argiris
AU - Čermák, Jaroslav
AU - Hellström-Lindberg, Eva
AU - Sanz, Guillermo
AU - Stauder, Reinhard
AU - Holm, Mette Skov
AU - Mittelman, Moshe
AU - Mądry, Krzysztof
AU - Malcovati, Luca
AU - Tatic, Aurelia
AU - Almeida, Antonio Medina
AU - Germing, Ulrich
AU - Savic, Aleksandar
AU - Gredelj Šimec, Njetočka
AU - Culligan, Dominic
AU - Itzykson, Raphael
AU - Guerci-Bresler, Agnes
AU - Slama, Borhane
AU - Droste, Jackie
AU - van Marrewijk, Corine
AU - van de Loosdrecht, Arjan
AU - Blijlevens, Nicole
AU - van Kraaij, Marian
AU - Bowen, David
AU - de Witte, Theo
AU - Smith, Alexandra Gwen
N1 - Copyright © 2019, Ferrata Storti Foundation.
Please email [email protected] for any changes made to this PURE entry.
PY - 2020/3/31
Y1 - 2020/3/31
N2 - Iron overload due to red blood cell transfusions is associated with morbidity and mortality in lower-risk myelodysplastic syndrome patients. Many studies suggested improved survival after iron chelation therapy, but valid data are limited. The aim of this study was to assess the effect of iron chelation on overall survival and hematological improvement in lower-risk myelodysplastic syndrome patients in the European MDS registry. We compared chelated patients with a contemporary, non-chelated control group within the European MDS registry, that met the eligibility criteria for starting iron chelation. A Cox proportional hazards model was used to assess overall survival, treating receipt of chelation as a time-varying variable. Additionally, chelated and non-chelated patients were compared using a propensity-score matched model. Of 2200 patients, 224 received iron chelation. The hazard ratio and 95% confidence interval for overall survival for chelated patients, adjusted for age, sex, comorbidity, performance status, cumulative red blood cell transfusions, IPSS-R, and presence of ringed sideroblasts was 0.50 (0.34-0.74). The propensity-score analysis, matched for age, sex, country, red blood cell transfusion intensity, ferritin level, comorbidity, performance status, and IPSS-R and additionally corrected for cumulative red blood cell transfusions and presence of ringed sideroblasts, demonstrated a significantly improved overall survival for chelated patients with a hazard ratio of 0.42 (0.27-0.63) compared to non-chelated patients. Up to 39% of chelated patients reached an erythroid response. In conclusion, our results suggest that iron chelation may improve overall survival and hematopoiesis in transfused lower-risk myelodysplastic syndrome patients. This trial was registered at www.clinicaltrials.gov as #NCT00600860.
AB - Iron overload due to red blood cell transfusions is associated with morbidity and mortality in lower-risk myelodysplastic syndrome patients. Many studies suggested improved survival after iron chelation therapy, but valid data are limited. The aim of this study was to assess the effect of iron chelation on overall survival and hematological improvement in lower-risk myelodysplastic syndrome patients in the European MDS registry. We compared chelated patients with a contemporary, non-chelated control group within the European MDS registry, that met the eligibility criteria for starting iron chelation. A Cox proportional hazards model was used to assess overall survival, treating receipt of chelation as a time-varying variable. Additionally, chelated and non-chelated patients were compared using a propensity-score matched model. Of 2200 patients, 224 received iron chelation. The hazard ratio and 95% confidence interval for overall survival for chelated patients, adjusted for age, sex, comorbidity, performance status, cumulative red blood cell transfusions, IPSS-R, and presence of ringed sideroblasts was 0.50 (0.34-0.74). The propensity-score analysis, matched for age, sex, country, red blood cell transfusion intensity, ferritin level, comorbidity, performance status, and IPSS-R and additionally corrected for cumulative red blood cell transfusions and presence of ringed sideroblasts, demonstrated a significantly improved overall survival for chelated patients with a hazard ratio of 0.42 (0.27-0.63) compared to non-chelated patients. Up to 39% of chelated patients reached an erythroid response. In conclusion, our results suggest that iron chelation may improve overall survival and hematopoiesis in transfused lower-risk myelodysplastic syndrome patients. This trial was registered at www.clinicaltrials.gov as #NCT00600860.
U2 - 10.3324/haematol.2018.212332
DO - 10.3324/haematol.2018.212332
M3 - Article
C2 - 31278207
SN - 0390-6078
VL - 105
SP - 640
EP - 651
JO - Haematologica-The hematology journal
JF - Haematologica-The hematology journal
IS - 3
ER -