Phase I/II Study of Stem-Cell Transplantation Using a Single Cord Blood Unit Expanded Ex Vivo With Nicotinamide

Author:

Horwitz Mitchell E.1,Wease Stephen2,Blackwell Beth2,Valcarcel David3,Frassoni Francesco4,Boelens Jaap Jan5,Nierkens Stefan5,Jagasia Madan6,Wagner John E.7,Kuball Jurgen5,Koh Liang Piu8,Majhail Navneet S.9,Stiff Patrick J.10,Hanna Rabi9,Hwang William Y.K.11,Kurtzberg Joanne1,Cilloni Daniela12,Freedman Laurence S.13,Montesinos Pau14,Sanz Guillermo3

Affiliation:

1. Duke University Medical Center, Durham, NC

2. Emmes Corporation, Rockville, MD

3. University Hospital Vall d’Hebron, Barcelona, Spain

4. Istituto Giannina Gaslini, Genoa, Italy

5. University Medical Center Utrecht, Utrecht, the Netherlands

6. Vanderbilt University Medical Center, Nashville, TN

7. University of Minnesota, Minneapolis, MN

8. National University Health System, Singapore

9. Cleveland Clinic, Cleveland, OH

10. Loyola University Medical Center, Chicago, IL

11. Singapore General Hospital, Singapore

12. University of Turin, Turin, Italy

13. Sheba Medical Center, Tel Hashomer, Israel

14. Hospital Universitario y Politécnic de La Fe, Valencia, Spain

Abstract

Purpose Increasing the number of hematopoietic stem and progenitor cells within an umbilical cord blood (UCB) graft shortens the time to hematopoietic recovery after UCB transplantation. In this study, we assessed the safety and efficacy of a UCB graft that was expanded ex vivo in the presence of nicotinamide and transplanted after myeloablative conditioning as a stand-alone hematopoietic stem-cell graft. Methods Thirty-six patients with hematologic malignancies underwent transplantation at 11 sites. Results The cumulative incidence of neutrophil engraftment at day 42 was 94%. Two patients experienced secondary graft failure attributable to viral infections. Hematopoietic recovery was compared with that observed in recipients of standard UCB transplantation as reported to the Center for International Blood and Marrow Transplant Research (n = 146). The median time to neutrophil recovery was 11.5 days (95% CI, 9 to 14 days) for recipients of nicotinamide-expanded UCB and 21 days (95% CI, 20 to 23 days) for the comparator ( P < .001). The median time to platelet recovery was 34 days (95% CI, 32 to 42 days) and 46 days (95% CI, 42 to 50 days) for the expanded and the comparator cohorts, respectively ( P < .001). The cumulative incidence of grade 2 to 4 acute graft-versus-host disease (GVHD) at day 100 was 44%, and grade 3 and 4 acute GVHD at day 100 was 11%. The cumulative incidence at 2 years of all chronic GVHD was 40%, and moderate/severe chronic GVHD was 10%. The 2-year cumulative incidences of nonrelapse mortality and relapse were 24% and 33%, respectively. The 2-year probabilities of overall and disease-free survival were 51% and 43%, respectively. Conclusion UCB expanded ex vivo with nicotinamide shortens median neutrophil recovery by 9.5 days (95% CI, 7 to 12 days) and median platelet recovery by 12 days (95% CI, 3 to 16.5 days). This trial establishes feasibility, safety, and efficacy of an ex vivo expanded UCB unit as a stand-alone graft.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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