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Umbilical cord blood expansion with nicotinamide provides long-term multilineage engraftment.

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Date
2014-07
Authors
Horwitz, Mitchell E
Chao, Nelson J
Rizzieri, David A
Long, Gwynn D
Sullivan, Keith M
Gasparetto, Cristina
Chute, John P
Morris, Ashley
McDonald, Carolyn
Waters-Pick, Barbara
Stiff, Patrick
Wease, Steven
Peled, Amnon
Snyder, David
Cohen, Einat Galamidi
Shoham, Hadas
Landau, Efrat
Friend, Etty
Peleg, Iddo
Aschengrau, Dorit
Yackoubov, Dima
Kurtzberg, Joanne
Peled, Tony
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(23 total)
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Abstract
<h4>Background</h4>Delayed hematopoietic recovery is a major drawback of umbilical cord blood (UCB) transplantation. Transplantation of ex vivo-expanded UCB shortens time to hematopoietic recovery, but long-term, robust engraftment by the expanded unit has yet to be demonstrated. We tested the hypothesis that a UCB-derived cell product consisting of stem cells expanded for 21 days in the presence of nicotinamide and a noncultured T cell fraction (NiCord) can accelerate hematopoietic recovery and provide long-term engraftment.<h4>Methods</h4>In a phase I trial, 11 adults with hematologic malignancies received myeloablative bone marrow conditioning followed by transplantation with NiCord and a second unmanipulated UCB unit. Safety, hematopoietic recovery, and donor engraftment were assessed and compared with historical controls.<h4>Results</h4>No adverse events were attributable to the infusion of NiCord. Complete or partial neutrophil and T cell engraftment derived from NiCord was observed in 8 patients, and NiCord engraftment remained stable in all patients, with a median follow-up of 21 months. Two patients achieved long-term engraftment with the unmanipulated unit. Patients transplanted with NiCord achieved earlier median neutrophil recovery (13 vs. 25 days, P < 0.001) compared with that seen in historical controls. The 1-year overall and progression-free survival rates were 82% and 73%, respectively.<h4>Conclusion</h4>UCB-derived hematopoietic stem and progenitor cells expanded in the presence of nicotinamide and transplanted with a T cell-containing fraction contain both short-term and long-term repopulating cells. The results justify further study of NiCord transplantation as a single UCB graft. If long-term safety is confirmed, NiCord has the potential to broaden accessibility and reduce the toxicity of UCB transplantation.<h4>Trial registration</h4>Clinicaltrials.gov NCT01221857.<h4>Funding</h4>Gamida Cell Ltd.
Type
Journal article
Subject
Fetal Blood
Transplantation Chimera
Humans
Hematologic Neoplasms
Niacinamide
Treatment Outcome
Transplantation Conditioning
Cord Blood Stem Cell Transplantation
Hematopoiesis
Graft Survival
Adult
Middle Aged
Young Adult
Permalink
https://hdl.handle.net/10161/24705
Published Version (Please cite this version)
10.1172/jci74556
Publication Info
Horwitz, Mitchell E; Chao, Nelson J; Rizzieri, David A; Long, Gwynn D; Sullivan, Keith M; Gasparetto, Cristina; ... Peled, Tony (2014). Umbilical cord blood expansion with nicotinamide provides long-term multilineage engraftment. The Journal of clinical investigation, 124(7). pp. 3121-3128. 10.1172/jci74556. Retrieved from https://hdl.handle.net/10161/24705.
This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.
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Scholars@Duke

Chao

Nelson Jen An Chao

Donald D. and Elizabeth G. Cooke Cancer Distinguished Research Professor
My research interests are in two broad areas, clinical hematopoietic stem cell and cord blood transplantation and in the laboratory studies related to graft vs. host disease and immune reconstitution. On the clinical side we are currently conducting approximately 50 different clinical protocols ranging from preparatory regimens, supportive care studies and disease specific protocols. Most of these clinical studies are centered around studies of the sources of stem cells and the methods to

John Patrick Chute

Adjunct Professor in the Department of Medicine
Gasparetto

Cristina Gasparetto

Professor of Medicine
Dr. Gasparetto performs both laboratory and clinical research in the field of multiple myeloma. Her primary research interests are in developing immunotherapy approaches to treating multiple myeloma particularly in conjunction with hematopoietic stem cell transplantation. Ongoing laboratory research projects include the development of dendritic cell vaccines and antibody therapies. Clinical studies include a recently approved trial involving vaccination with autologous dendritic cells pulse
Horwitz

Mitchell Eric Horwitz

Professor of Medicine
Allogeneic stem cell transplantation using umbilical cord blood grafts; Allogenic stem cell transplantation for Sickle Cell Disease; Prevention of acute graft versus host disease through donor stem cell graft manipulation; Improving immune recovery following alternative donor stem cell transplantation using donor graft manipulation or third party thymus transplantation.
Kurtzberg

Joanne Kurtzberg

Jerome S. Harris Distinguished Professor of Pediatrics
Dr. Kurtzberg conducts both clinical and laboratory-based translational research efforts, all involving various aspects of normal and malignant hematopoiesis. In the laboratory, her early work focused on studies determining the mechanisms that regulate the choice between the various pathways of differentiation available to the pluripotent hematopoietic stem cell. Her laboratory established a CD7+ cell line, DU.528, capable of multilineage differentiation as well as self-renewal, and subse
Long

Gwynn Douglas Long

Professor of Medicine
1. High dose therapy and autologous and allogeneic stem cell rescue for hematologic malignancies (especially multiple myeloma) and solid tumors. 2. Non-myeloablative allogeneic transplants for hematologic malignancies and solid tumors. 3. Supportive care for hematopoietic stem cell transplants. 4. Prevention and therapy of graft versus host disease.
Rizzieri

David Alan Rizzieri

Professor of Medicine
My research interests focus on the care of patients with hematologic malignancies, both with and without the use of bone marrow or stem cell transplantation. I focus my research efforts on new approaches to manipulate minimal residual disease.Recent endeavors have included: Phase one trials with novel anti-cancer agents targeting aurora kinases, tyrosine kinases, mtor, VEGF, and raf/ras pathways  New monoclonal antibodies targeting tumor stroma rat
Sullivan

Keith Michael Sullivan

James B. Wyngaarden Distinguished Professor of Medicine
Research areas Late effects of cancer treatment and stem cell transplantation  Chronic graft-versus-host disease  Transplantation for sickle cell and autoimmune diseases  Knowledge engineering OverviewEarly on, Dr. Sullivan and the team at Fred Hutchinson Cancer Research Center developed a systematic investigative approach for the diagnosis and treatment of chronic graft-versus-host
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