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NCT Number: NCT02757989

Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Myelodysplastic Syndrome Low Risk

Comparison of survival in patients with or without a matched donor at 36 months

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Key information

Conditions

MDS

Age range

18 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU d'Amiens, Amiens, France

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed Informed consent
  • Classical IPSS intermediate 1 or low myelodysplastic syndrome associated with at least one poor prognosis feature:
  • Intermediate or higher risk revised IPSS
  • RBC transfusion dependent anemia and failure to 2 or more lines or therapy (including EPO, Lenalidomide or demethylating agent…)
  • thrombocytopenia < 20 G/L requiring transfusion
  • neutropenia < 0.5 G/L associated with severe infection (defined as requiring hospitalization)
  • Patient aged ≥ 18 and < 70 years For young patients, 18-45 years, Fanconi disease and dyskeratosis should be ruled out
  • Patient for whom a transplantation from a matched donor, (8/8 (HLA A, B, C, DRB1) identical at molecular level)unrelated donor or matched sibling), is considered irrespective of donor availability
  • Performance status 0-2 on the Eastern Cooperative Oncology Group (ECOG) Scale (At time of screening)
  • Negative pregnancy and adequate contraception (including in male patients wishing to father), if relevant.
  • Wash-out of at least 30 days since a previous treatment with Vidaza, Lenalidomide, EPO or any other treatment inducing cytopenias.

Exclusion criteria

  • MDS classified according to classical IPSS as intermediate 2 or High risk
  • Transformation in Acute myeloid Leukemia (AML)
  • Severe active infection or any other uncontrolled severe condition.
  • Organ dysfunctions including the following
  • Hepatic : total bilirubin > 2 times upper limit of normal (ULN) (except moderate unconjugated hyperbilirubinemia due to intra medullary hemolysis or Gilbert syndrome) , alanine transaminase (ALT) and aspartate transaminase (AST) > 3xULN
  • Symptomatic respiratory chronic failure
  • Symptomatic cardiac failure
  • Renal clearance < 60ml/min
  • Prior malignancy (except in situ cervix carcinoma, limited basal cell carcinoma, or other tumors if not active during the last 3 years)
  • MDS with the following causal germline disease : Fanconi anemia, GATA2 related syndromes and telomere disorders

Treatment and study plan

transplantation

Other

allogeneic hematopoietic stem cell transplantation in patients with donor

Primary outcomes

  1. overall survival

    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

Secondary outcomes

  1. quality of life

    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

  2. number of patients with complete response at 36 month

    Time frame: 36 months

    comparison between patients with or without a donor for cumulative incidence of complete response at 36 month

  3. number of patients with transformation in AML 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

  4. proportion of patients with iron overload

    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

  5. evolution of innovative iron markers including Non-transferrin binding iron (NTBI), labile plasmatic Iron (LPI) and Hepcidine

    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.

  6. efficiency of chelation

    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

  7. number of patients with adverse events grade III and IV as assessed by CTCAE v4.0

    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

Sponsors and collaborators

Lead sponsor

Groupe Francophone des Myelodysplasies

Other

Collaborators

  • Neovii Biotech
  • Novartis

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2024
Study completion
2024
First posted
May 2, 2016
Registry last updated
Aug 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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