Decitabine and Umbilical Cord Blood for Poor Graft Function Post Allo-HSCT

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age16-65
SponsorThe First Affiliated Hospital of Soochow University

About this trial

This randomized trial aimed at validating the efficacy and safety of low-dose decitabine, together with umbilical cord blood in PGF post allo-HSCT patients.

Eligibility criteria

Qualifiers

Diagnosed as PGF at day 28 post-HSCT or later. PGF was defined as two or three cytopenias, absolute neutrophil count ≤ 1.5 × 109/L, platelet count ≤ 30 × 109/L, hemoglobin ≤ 85g/L, lasting for more than 2 consecutive weeks;

Full donor chimerism;

Primary disease in remission;

No severe GVHD and relapse.

Disqualifiers

Allergic to decitabine or any components of frozen preservation of umbilical cord blood;

Active infections;

Uncontrolled GVHD;

Severe organ dysfunction;

Trial design

Treatments tested in this trial

  • decitabine
  • umbilical cord blood
  • Granulocyte-colony stimulating factor
  • Recombinant human thrombopoietin / thrombopoietin receptor agonist
  • Recombinant human erythropoietin

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations