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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

Primary Purpose

Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS)

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Haplo-Cord Transplant
Matched Unrelated Donor Transplant
Sponsored by
University of Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myeloid Leukemia (AML) focused on measuring Acute Myeloid Leukemia (AML), High-Risk Myelodysplastic Syndrome (MDS), hematopoietic cell transplantation, haplo-cord search, matched unrelated donor search

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of Chicago Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Haplo-Cord Search

Matched Unrelated Donor Search (MUD)

Arm Description

If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant.

If subject meets the inclusion criteria and consents, will undergo a MUD transplant.

Outcomes

Primary Outcome Measures

Time to Transplant
Time to transplant will be measured from time of date of formal request to stem cell infusion date. Will also capture time from preliminary search to both formal search and transplant date.

Secondary Outcome Measures

Percentage of Patients Who Undergo Hematopoietic Cell Transplantation (HCT)
Compare percentage of patients who undergo HCT in each study cohort
Estimated Survival Time
Overall survival time was estimated from date of randomization and from date of transplant using Kaplan-Meier method.

Full Information

First Posted
January 4, 2016
Last Updated
February 22, 2021
Sponsor
University of Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT02648932
Brief Title
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
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Terminated
Why Stopped
Poor accrual
Study Start Date
February 4, 2016 (Actual)
Primary Completion Date
April 2020 (Actual)
Study Completion Date
April 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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)
Detailed Description
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS)
Keywords
Acute Myeloid Leukemia (AML), High-Risk Myelodysplastic Syndrome (MDS), hematopoietic cell transplantation, haplo-cord search, matched unrelated donor search

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Haplo-Cord Search
Arm Type
Other
Arm Description
If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant.
Arm Title
Matched Unrelated Donor Search (MUD)
Arm Type
Other
Arm Description
If subject meets the inclusion criteria and consents, will undergo a MUD transplant.
Intervention Type
Biological
Intervention Name(s)
Haplo-Cord Transplant
Intervention Description
For conditioning regimens, haplo-identical grafts will be selected by the Miltenyi Device
Intervention Type
Procedure
Intervention Name(s)
Matched Unrelated Donor Transplant
Primary Outcome Measure Information:
Title
Time to Transplant
Description
Time to transplant will be measured from time of date of formal request to stem cell infusion date. Will also capture time from preliminary search to both formal search and transplant date.
Time Frame
Through one year after formal search
Secondary Outcome Measure Information:
Title
Percentage of Patients Who Undergo Hematopoietic Cell Transplantation (HCT)
Description
Compare percentage of patients who undergo HCT in each study cohort
Time Frame
Through one year after formal search
Title
Estimated Survival Time
Description
Overall survival time was estimated from date of randomization and from date of transplant using Kaplan-Meier method.
Time Frame
From date of randomization up to 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria for Search Phase: Diagnosis of acute myeloid leukemia (AML) or high or very high-risk MDS by international prognostic scoring system revised for whom transplant is recommended 18 years of age or older 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). 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) Ability to understand and the willingness to sign a written informed consent document for the Search Phase. Patient willing to consider HCT A preliminary search has identified: 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 At least one potential 8/8 HLA-matched (HLA-A, -B, -C, and -DRB1) unrelated donor with a probability of 70% AND Availability of a potential related haploidentical donor. Exclusion Criteria for Search Phase: Prior formal search was instituted Diagnosis of acute promyelocytic leukemia (APL) Known HLA matched related donor without contraindications to donate Life expectancy severely limited by concomitant illness or uncontrolled infection Inclusion Criteria for Transplant Phase 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. For MDS. IPSS-revised criteria of high or very high at diagnosis. Subject meets institutional criteria for transplant and has acceptable organ and marrow function as defined below: Serum bilirubin < 2.0mg/dL unless Gilberts disease Creatinine Clearance > 45 mL/min.1.73m2 as estimated by modified MDRD equation Left ventricular function 40% or greater DLCO corrected for hemoglobin >50% KPS 70% or greater An adequate graft for the defined donor type 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. 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. Written informed consent for the transplant phase Exclusion Criteria for Transplant Phase Life expectancy severely limited by concomitant illness or uncontrolled infection HIV-positive
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Artz, MD
Organizational Affiliation
University of Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Chicago Cancer Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States

12. IPD Sharing Statement

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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

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