About this trial

The purpose of this study is to see if see if adding the specific combination of donors can result in acceptable levels of survival without evidence of disease.

Eligibility criteria

Qualifiers

Antecedent hematological disease (e.g., myelodysplasia (MDS))

Treatment-related

Complete Remission (CR1) with poor or intermediate-risk cytogenetics or molecular markers (e.g. Flt 3 mutation, 11q23, del 5, del 7, TP53 mutations, complex cytogenetics)

Participants must be in CR1, CR2, CR3 or CRi

Disqualifiers

Creatinine clearance < 40ml/min (Cockcroft-Gault)

Bilirubin > 2X institutional upper limit of normal unless Gilbert syndrome

AST (SGOT) > 3X institutional upper limit of normal

ALT (SGPT) > 3X institutional upper limit of normal

Trial design

Treatments tested in this trial

  • Haplo-Identical / Cord Blood Transplant

Treatment groups

36 Participants
are divided into 1 treatment group

Locations

1
Case Comprehensive Cancer Center, University Hospitals Cleveland Medical Center Seidman Cancer Center44106, ClevelandOhio, United States

Sponsors and collaborators

Case Comprehensive Cancer Center

Lead sponsor