transplantation
Otherallogeneic hematopoietic stem cell transplantation in patients with donor
NCT Number: NCT02757989
Comparison of survival in patients with or without a matched donor at 36 months
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Notify Me18 year–69 year
All sexes
Interventional
Not applicable
CHU d'Amiens, Amiens, France
Patients with a matched donor (8/8 at molecular level unrelated donor or matched sibling) received an allogeneic hematopoietic stem cell transplantation.
Patients without a matched donor received the best available treatment. All patients will be followed at least 36 months or until the end of the study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
allogeneic hematopoietic stem cell transplantation in patients with donor
Time frame: 36 months
comparison of overall survival in patients with or without a matched donor (8/8 unrelated donor or matched sibling) at 36 months
Time frame: 12, 24 and 36 months
comparison of quality of life in patients with or without a matched donor, quality of life assessed by questionnaire (EORTC version 3) at inclusion, 12, 24 and 36 months
Time frame: 36 months
comparison between patients with or without a donor for cumulative incidence of complete response at 36 month
Time frame: 36 months
comparison between patients with or without a donor for cumulative incidence of transformation in AML at 36 month
Time frame: 16 months
proportion of patients with iron overload (Serum Ferritin (SF)>1000 ng/mL or Red Blood Cells transfusion>20) at time of inclusion and at 16 month after inclusion for non-transplanted patients and 12 months post-transplant for transplanted patients
Time frame: 3 and 16 months
evolution of innovative iron markers including Non-transferrin binding iron (NTBI), labile plasmatic Iron (LPI) and Hepcidine measured at time of inclusion, at 3 month and 16 month post-inclusion for all patients; In transplanted patients these markers will be measured just before conditioning regimen (J-5), Just before the transplantation (J0), at D7, 30, 100 and 12 month after transplant.
Time frame: 3 and 16 months
the effect of chelation will be assessed at 3 month after inclusion for all patient and post transplant by measuring Serum ferritin level
Time frame: 36 months
comparison between patients with or without a donor for number of Grade III and IV toxicities (hematological and non-hematological) recorded according to NCI CTCAE criteria versions 4.0 during the 36 months
Groupe Francophone des Myelodysplasies
Other
Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Low or Intermediate-1 Myelodysplastic Syndrome: A Prospective Multicenter Phase II Study Based on Donor Availability on Behalf of the GFM & SFGM-TC
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