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Selection of Allogeneic Hematopoietic Cell Donors Based on KIR and HLA Genotypes

Not Applicable
Active, not recruiting
Conditions
Leukemia
Interventions
Genetic: KIR genotyping
Genetic: HLA genotyping
Registration Number
NCT02450708
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

This study tests whether adding certain genetic factors to the process of picking a stem cell donor can decrease the chances that the patient's leukemia will come back after bone marrow transplantation. Stem cell donors are "matched" based on genes called human leukocyte antigens (HLA).

Currently, donors are selected largely on the basis of HLA gene typing alone. There is published data to show that donors with specific other genes called killer immunoglobulin-like receptors (KIR) may protect AML patients from having their leukemia return after a transplant. In this study, the best HLA matched donors will be tested for the KIR genes. If there is more than 1 donor available, a recommendation will be provided to study doctors as to which donors have potentially favorable KIR genes. The study doctors may or may not choose to use this donor for transplant or not based on his/her own judgment. Transplant care will not change otherwise as a result of this study.

This study is being done to demonstrate that AML patients who have donors with specific KIR and HLA genes will have a better outcome following transplant.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
511
Inclusion Criteria

RECIPIENT

  • Persons of all ages are eligible for this study.
  • Patient must have diagnosis of acute myelogenous leukemia (AML) at MSK or a collaborating treating institution. Patients with de novo AML or AML with preceding myelodysplastic syndrome (MDS) are eligible.
  • Patient must be a potential candidate for an unrelated transplantation procedure at the time of enrollment even though patient may not be eligible for transplantation in the future due to relapse or presence of co-morbidity(ies).
  • An unrelated donor does not need to be identified at the time of enrollment. If an HLA-compatible unrelated donor is not identified for the patient, the patient will be removed from the study.
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Exclusion Criteria
  • Recipients with an available sibling donor matched at HLA-A, HLA-C, and HLA-DRB1 (excluding identical twin siblings).
  • Patients for whom post-transplant treatment is planned are not excluded from enrollment.
  • Patients with prior allogeneic hematopoietic cell transplantation for AML. Note: Patients who have undergone prior hematopoietic cell transplantation for a diagnosis other than AML are still eligible for this study.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
For patients with >1 HLA-compatible donor for URD HCTKIR genotypingFor patients with 1 or more donor candidates, KIR genotyping may be performed for up to 5 donors. For patients with HLA-B alleles harboring the Bw4 epitope, KIR3DL1 allele typing will be performed at MSKCC.
For patients with >1 HLA-compatible donor for URD HCTHLA genotypingFor patients with 1 or more donor candidates, KIR genotyping may be performed for up to 5 donors. For patients with HLA-B alleles harboring the Bw4 epitope, KIR3DL1 allele typing will be performed at MSKCC.
For patients with 1 HLA-compatible donor for URD HCTHLA genotypingFor patients with 1 URD: donor KIR genotyping will be performed on the donor. Because donor selection will not depend on KIR/HLA genotyping, completion of donor KIR genotyping is not required prior to transplant.
Primary Outcome Measures
NameTimeMethod
relapse1 year

Demonstration of evidence of leukemia (\>5% blasts in the bone marrow, peripheral blood blasts, or development of extramedullary disease) after initial achievement of either a CR or CRi.

Secondary Outcome Measures
NameTimeMethod
overall survival1 year

Overall survival (OS). The time from study enrollment until death from any cause.

Trial Locations

Locations (10)

Baylor University Medical Center

🇺🇸

Dallas, Texas, United States

Md Anderson Cancer Center

🇺🇸

Houston, Texas, United States

Dana Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

University of Washington School of Medicine

🇺🇸

Seattle, Washington, United States

Hackensack University Medical Center Cancer Center

🇺🇸

Hackensack, New Jersey, United States

Moffitt Cancer Center

🇺🇸

Tampa, Florida, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Mayo Clinic Cancer Center

🇺🇸

Rochester, Minnesota, United States

Duke University Medical Center

🇺🇸

Durham, North Carolina, United States

Ohio State University

🇺🇸

Columbus, Ohio, United States

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