The Rapid Study: Randomized Phase II Study To Expedite Allogeneic Transplant With Immediate Haploidentical Plus Unrelated Cord Donor Search Versus Matched Unrelated Donor Search For AML And High-Risk MDS Patients

  • Interventional
  • Recruiting
  • NCT02648932
Eligibility Details Visit Clinicaltrials.gov

The Rapid Study: Randomized (RA) Phase (P) II Study To Expedite Allogeneic Transplant With Immediate (I) Haploidentical Plus Unrelated Cord Donor (D) Search Versus Matched Unrelated Donor Search For AML And High-Risk MDS Patients

The study seeks to compare time from formal search to hematopoietic cell transplantation (HCT) for patients 18 years and older, randomized between haplo-cord search and matched unrelated donor (MUD) search for patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS)

Primary Objectives

     To compare time from formal search to hematopoietic cell transplantation (HCT) for patients 18 years and older, randomized between haplo-cord search and matched unrelated donor (MUD) search for patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS)

     Secondary Objectives

        - To compare the percentage of patients who undergo HCT in each study cohort

        - To evaluate overall survival from time to randomization by study cohort

Gender
All

Age Group
18 Years and up

Accepting Healthy Volunteers?
No

Inclusion Criteria for Search Phase:

         1. Diagnosis of acute myeloid leukemia (AML) or high or very high-risk MDS by international prognostic scoring system revised for whom transplant is recommended

         2. 18 years of age or older

         3. Subject is likely to be considered for allogeneic transplant in the opinion of the transplant physician (based on age of patient, health, cytogenetics, and/or molecular characteristics).

         4. Karnofsky Performance Status (KPS) >/= 70% at time of enrollment. An exception will be made for those with lower KPS at enrollment with an acute worsening that is likely to resolve in the treating physicians judgment (e.g., reversible infection,trauma, medication reaction, etc)

         5. Ability to understand and the willingness to sign a written informed consent document for the Search Phase.

         6. Patient willing to consider HCT

         7. A preliminary search has identified:

             1. An appropriate minimum 4/6 matched umbilical cord unit at intermediate resolution at HLA-A and B, and high resolution at HLA-DRB with a cell dose above 1 x 10(7) TNC/kg for a single umbilical cord blood (UCB) transplant AND

             2. At least one potential 8/8 HLA-matched (HLA-A, -B, -C, and -DRB1) unrelated donor with a probability of 70% AND

             3. Availability of a potential related haploidentical donor.

        Exclusion Criteria for Search Phase:

         1. Prior formal search was instituted

         2. Diagnosis of acute promyelocytic leukemia (APL)

         3. Known HLA matched related donor without contraindications to donate

         4. Life expectancy severely limited by concomitant illness or uncontrolled infection

        Inclusion Criteria for Transplant Phase

         1. High-risk AML for which transplant is recommend based on cytogenetic, molecular and morphologic features. Patients must meet institutional standards for disease control prior to transplant.

         2. For MDS. IPSS-revised criteria of high or very high at diagnosis.

         3. Subject meets institutional criteria for transplant and has acceptable organ and marrow function as defined below:

             1. Serum bilirubin < 2.0mg/dL unless Gilberts disease

             2. Creatinine Clearance > 45 mL/min.1.73m2 as estimated by modified MDRD equation

             3. Left ventricular function 40% or greater

             4. DLCO corrected for hemoglobin >50%

             5. KPS 70% or greater

         4. An adequate graft for the defined donor type

             1. Haplo-cord requires a haploidentical adult donor of 14 years of age and at least 50 kg, and a cord blood unit with at least 1.0 x 10(7) TNC/kg and a match of at least 4/6 by intermediate resolution for HLA-A and B and high resolution at DRB1. Donor provides standard of care consent for harvest following institutional policy. Any donor samples or donor research data would be obtained on separate donor research protocol.

             2. For MUD requires a 7/8 or 8/8 HLA matched unrelated donor with high resolution matching at HLA-A, -B, -C, and DRB1. DP matching or DP permissive should be achieved when possible using T-cell epitope strategy.

         5. Written informed consent for the transplant phase

        Exclusion Criteria for Transplant Phase

         1. Life expectancy severely limited by concomitant illness or uncontrolled infection

         2. HIV-positive

At a Glance

National Government IDNCT02648932

IRB#IRB15-0866

Lead SponsorUniversity of Chicago

Lead PhysicianAndrew Artz

Collaborator(s)N/A

EligibilityAll
18 Years and up
Recruiting