Alternative donor transplantation after reduced intensity conditioning: results of parallel phase 2 trials using partially HLA-mismatched related bone marrow or unrelated double umbilical cord blood grafts

Author:

Brunstein Claudio G.1,Fuchs Ephraim J.2,Carter Shelly L.3,Karanes Chatchada4,Costa Luciano J.5,Wu Juan3,Devine Steven M.6,Wingard John R.7,Aljitawi Omar S.8,Cutler Corey S.9,Jagasia Madan H.10,Ballen Karen K.11,Eapen Mary12,O'Donnell Paul V.13,

Affiliation:

1. Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN;

2. Sidney Kimmel Cancer Center, Johns Hopkins University, Baltimore, MD;

3. The Emmes Corporation, Rockville, MD;

4. City of Hope National Medical Center, Duarte, CA;

5. Medical University of South Carolina, Charleston, SC;

6. The Ohio State University, Columbus, OH;

7. University of Florida College of Medicine, Gainesville, FL;

8. The University of Kansas, Kansas City, KS;

9. Dana-Farber Cancer Institute, Boston, MA;

10. Vanderbilt University, Nashville, TN;

11. Massachusetts General Hospital, Boston, MA;

12. Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI; and

13. Fred Hutchinson Cancer Center, University of Washington, Seattle, WA

Abstract

Abstract The Blood and Marrow Transplant Clinical Trials Network conducted 2 parallel multicenter phase 2 trials for individuals with leukemia or lymphoma and no suitable related donor. Reduced intensity conditioning (RIC) was used with either unrelated double umbilical cord blood (dUCB) or HLA-haploidentical related donor bone marrow (Haplo-marrow) transplantation. For both trials, the transplantation conditioning regimen incorporated cyclophosphamide, fludarabine, and 200 cGy of total body irradiation. The 1-year probabilities of overall and progression-free survival were 54% and 46%, respectively, after dUCB transplantation (n = 50) and 62% and 48%, respectively, after Haplo-marrow transplantation (n = 50). The day +56 cumulative incidence of neutrophil recovery was 94% after dUCB and 96% after Haplo-marrow transplantation. The 100-day cumulative incidence of grade II-IV acute GVHD was 40% after dUCB and 32% after Haplo-marrow transplantation. The 1-year cumulative incidences of nonrelapse mortality and relapse after dUCB transplantation were 24% and 31%, respectively, with corresponding results of 7% and 45%, respectively, after Haplo-marrow transplantation. These multicenter studies confirm the utility of dUCB and Haplo-marrow as alternative donor sources and set the stage for a multicenter randomized clinical trial to assess the relative efficacy of these 2 strategies. The trials are registered at www.clinicaltrials.gov under NCT00864227 (BMT CTN 0604) and NCT00849147 (BMT CTN 0603).

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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