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Spots Global Cancer Trial Database for Selecting a Favorable KIR Donor in Unrelated HCT for AML

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Trial Identification

Brief Title: Selecting a Favorable KIR Donor in Unrelated HCT for AML

Official Title: KIR Genotyping for Unrelated Donor (URD) Selection Prior to Hematopoietic Cell Transplantation (HCT) for AML: Selecting a Favorable KIR Donor

Study ID: NCT01288222

Interventions

KIR genotype

Study Description

Brief Summary: Donors with favorable KIR B haplotype gene content have yielded reduced relapse risk and improved leukemia free survival (LFS) in retrospective analyses of unrelated donor (URD) hematopoietic cell transplantation (HCT) for acute myelogenous leukemia (AML). Specifically, donors with more KIR B gene content and those who are homozygous for the centromeric (Cen) B haplotype genes (as opposed to the telomeric (Tel) genes confer the most protective effect. This study proposes to prospectively test and validate the utility and effectiveness of further informing URD identification and selection by KIR genotyping as a supplement to HLA matching and the other variables known or suspected to indicate the best URD for a patient. Hypotheses: 1. Favorable KIR donors will improve protection against relapse and improve leukemia free survival (LFS) after URD HCT for AML. 2. Directed study procedures for rapid KIR genotyping and reporting to searching Transplant Centers (TC) can inform donor search and selection without delay in donor availability for HCT.

Detailed Description: Transplant Centers will select the best HLA matched, and as appropriate, preferred KIR donor.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Mayo Clinic - Scottsdale, Scottsdale, Arizona, United States

Colorado Blood Cancer Institute, Denver, Colorado, United States

Emory University, Atlanta, Georgia, United States

University of Chicago Medical Center Cancer Center, Chicago, Illinois, United States

Indiana University Simon Cancer Center, Indianapolis, Indiana, United States

Kansas University Cancer Center, Kansas City, Kansas, United States

Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States

Mayo Clinic Cancer Center, Rochester, Minnesota, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Hackensack University Medical Center, Hackensack, New Jersey, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

New York Presbyterian Weill Cornell Medical Center, New York, New York, United States

Cleveland Clinic, Cleveland, Ohio, United States

Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States

University of Pennsylvania, Philadelphia, Pennsylvania, United States

Baylor Sammons Cancer Center, Dallas, Texas, United States

M.D. Anderson Cancer Center, Houston, Texas, United States

Methodist Healthcare System of San Antonio, San Antonio, Texas, United States

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States

Contact Details

Name: Daniel Weisdorf, M.D.

Affiliation: Masonic Cancer Center, University of Minnesota

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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