Comparison of haploidentical and umbilical cord blood transplantation after myeloablative conditioning

Author:

Wagner John E.1,Ballen Karen K.2,Zhang Mei-Jie3,Allbee-Johnson Mariam4,Karanes Chatchada5,Milano Filippo6ORCID,Verneris Michael R.7,Eapen Mary4,Brunstein Claudio G.1

Affiliation:

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

2. Division of Hematology/Oncology, University of Virginia School of Medicine, Charlottesville, VA;

3. Division of Biostatics, Institute for Heath and Equity,

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

5. Department of Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA;

6. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA; and

7. Bone Marrow Transplant Program, Center for Cancer and Blood Disorders, Department of Pediatrics, University of Colorado School of Medicine, Denver, CO

Abstract

Abstract Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) has emerged as an important treatment modality. Most reports comparing haplo-HSCT with posttransplant cyclophosphamide (PTCy) and other donor sources have focused on outcomes in older adults treated with reduced intensity conditioning. Therefore, in the current study, we evaluated outcomes in patients with hematological malignancy treated with myeloablative conditioning prior to haplo- (n = 375) or umbilical cord blood (UCB; n = 333) HSCT. All haplo recipients received a 4 of 8 HLA-matched graft, whereas recipients of UCB were matched at 6-8/8 (n = 145) or ≤5/8 (n = 188) HLA antigens. Recipients of 6-8/8 UCB transplants were younger (14 years vs 21 and 29 years) and more likely to have lower comorbidity scores compared with recipients of ≤5/8 UCB and haplo-HSCT (81% vs 69% and 63%, respectively). UCB recipients were more likely to have acute lymphoblastic leukemia and transplanted in second complete remission (CR), whereas haplo-HSCT recipients were more likely to have acute myeloid leukemia in the first CR. Other characteristics, including cytogenetic risk, were similar. Survival at 3 years was similar for the donor sources (66% haplo- and 61% after ≤5/8 and 58% after 6-8/8 UCB). Notably, relapse at 3 years was lower in recipients of ≤5/8 UCB (21%, P = .03) compared with haplo- (36%) and 6-8/8 UCB (30%). However, nonrelapse mortality was higher in ≤5/8 UCB (21%) compared with other groups (P < .0001). These data suggest that haplo-HSCT with PTCy after myeloablative conditioning provides an overall survival outcome comparable to that after UCB regardless HLA match group.

Publisher

American Society of Hematology

Subject

Hematology

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