Transplantation of ex vivo expanded cord blood

Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expan...

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Veröffentlicht in:Biology of blood and marrow transplantation 2002-01, Vol.8 (7), p.368-376
Hauptverfasser: Shpall, Elizabeth J, Quinones, Ralph, Giller, Roger, Zeng, Chan, Baron, Anna E, Jones, Roy B, Bearman, Scott I, Nieto, Yago, Freed, Brian, Madinger, Nancy, Hogan, Christopher J, Slat-Vasquez, Vicki, Russell, Peggy, Blunk, Betsy, Schissel, Deborah, Hild, Elaine, Malcolm, Janet, Ward, William, McNiece, Ian K
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container_end_page 376
container_issue 7
container_start_page 368
container_title Biology of blood and marrow transplantation
container_volume 8
creator Shpall, Elizabeth J
Quinones, Ralph
Giller, Roger
Zeng, Chan
Baron, Anna E
Jones, Roy B
Bearman, Scott I
Nieto, Yago
Freed, Brian
Madinger, Nancy
Hogan, Christopher J
Slat-Vasquez, Vicki
Russell, Peggy
Blunk, Betsy
Schissel, Deborah
Hild, Elaine
Malcolm, Janet
Ward, William
McNiece, Ian K
description Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors. Biol Blood Marrow Transplant 2002;8(7):368-76.
doi_str_mv 10.1053/bbmt.2002.v8.pm12171483
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CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors. 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CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors. Biol Blood Marrow Transplant 2002;8(7):368-76.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12171483</pmid><doi>10.1053/bbmt.2002.v8.pm12171483</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Antigens, CD34
Breast Neoplasms - mortality
Breast Neoplasms - therapy
Cell Culture Techniques - methods
Child
Child, Preschool
Cord Blood Stem Cell Transplantation - methods
Cord Blood Stem Cell Transplantation - mortality
Feasibility Studies
Female
Fetal Blood - cytology
Graft Survival
Hematologic Neoplasms - mortality
Hematologic Neoplasms - therapy
Humans
Infant
Leukocyte Count
Male
Middle Aged
Neutrophils - cytology
title Transplantation of ex vivo expanded cord blood
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