Augmentation of umbilical cord blood (UCB) transplantation with ex vivo-expanded UCB cells: results of a phase 1 trial using the AastromReplicell System

被引:214
作者
Jaroscak, J
Goltry, K
Smith, A
Waters-Pick, B
Martin, PL
Driscoll, TA
Howrey, R
Chao, N
Douville, J
Burhop, S
Fu, PF
Kurtzberg, J
机构
[1] Duke Univ, Med Ctr, Pediat Program, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Adult Bone Marrow Transplant Program, Durham, NC 27710 USA
[3] Aastrom Biosci, Ann Arbor, MI USA
[4] Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
关键词
D O I
10.1182/blood-2001-12-0290
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic stem cell transplantation with umbilical cord blood (UCB) cells is limited by the cell dose a single unit provides recipients. Ex vivo expansion is one strategy to increase the number of cells available for transplantation. Aastrom Bio-sciences developed an automated continuous perfusion culture device for expansion of hematopoietic stem cells (HSCs). Cells are expanded in media supplemented with fetal bovine serum, horse serum, PIXY321, flt-3 ligand, and erythropoietin. We performed a phase 1 trial augmenting conventional UCB transplants with ex vivo-expanded cells. The 28 patients were enrolled on the trial between October 8, 1997 and September 30,1998. UCB cells were expanded in the device, then administered as a boost to the conventional graft on posttransplantation day 12. While expansion of total cells and colony-forming units (CFUs) occurred in all cases, the magnitude of expansion varied considerably. The median fold increase was 2.4 (range, 1.0-8.5) in nucleated cells, 82 (range, 4.6-266.4) in CFU granulocyte-macrophages, and 0.5 (range, 0.09-2.45) in CD34(+) lineage negative (lin(-)) cells. CD3(+) cells did not expand under these conditions. Clinical-scale ex vivo expansion of UCB is feasible, and the administration of ex vivo-expanded cells is well tolerated. Augmentation of UCB transplants with ex vivo-expanded cells did not alter the time to myeloid, erythroid, or platelet engraftment in 21 evaluable patients. Recipients of ex vivo-expanded cells continue to have durable engraftment with a median follow-up of 47 months (range, 41-51 months). A randomized phase 2 study will determine whether augmenting UCB transplants with ex vivo-expanded UCB cells is beneficial. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:5061 / 5067
页数:7
相关论文
共 37 条
[1]   Ex-vivo expansion of bone marrow progenitor cells for hematopoietic reconstitution following high-dose chemotherapy for breast cancer [J].
Bachier, CR ;
Gokmen, E ;
Teale, J ;
Lanzkron, S ;
Childs, C ;
Franklin, W ;
Shpall, E ;
Douville, J ;
Weber, S ;
Muller, T ;
Armstrong, D ;
LeMaistre, CF .
EXPERIMENTAL HEMATOLOGY, 1999, 27 (04) :615-623
[2]   Placental and/or umbilical cord blood: An alternative source of hematopoietic stem cells for transplantation [J].
Cairo, MS ;
Wagner, JE .
BLOOD, 1997, 90 (12) :4665-4678
[3]  
Champlin R., 1995, Blood, V86, p295A
[4]   CONDITIONS CONTROLLING PROLIFERATION OF HEMATOPOIETIC STEM-CELLS INVITRO [J].
DEXTER, TM ;
ALLEN, TD ;
LAJTHA, LG .
JOURNAL OF CELLULAR PHYSIOLOGY, 1977, 91 (03) :335-344
[5]   Hematopoietic potential of cryopreserved and ex vivo manipulated umbilical cord blood progenitor cells evaluated in vitro and in vivo [J].
DiGiusto, DL ;
Lee, R ;
Moon, J ;
Moss, K ;
OToole, T ;
Voytovich, A ;
Webster, D ;
Mule, JJ .
BLOOD, 1996, 87 (04) :1261-1271
[6]   Cord blood transplantation study (COBLT): Cord blood bank standard operating procedures [J].
Fraser, JK ;
Cairo, MS ;
Wagner, EL ;
McCurdy, PR ;
Baxter-Lowe, LA ;
Carter, SL ;
Kernan, NA ;
Lill, MC ;
Slone, V ;
Wagner, JE ;
Wallas, CH ;
Kurtzberg, J .
JOURNAL OF HEMATOTHERAPY, 1998, 7 (06) :521-561
[7]   LONG-TERM CULTURE OF HUMAN-BONE MARROW-CELLS [J].
GARTNER, S ;
KAPLAN, HS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (08) :4756-4759
[8]   Outcome of cord-blood transplantation from related and unrelated donors [J].
Gluckman, E ;
Rocha, V ;
BoyerChammard, A ;
Locatelli, F ;
Arcese, W ;
Pasquini, R ;
Ortega, J ;
Souillet, G ;
Ferreira, E ;
Laporte, JP ;
Fernandez, M ;
Chastang, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :373-381
[9]  
Goltry KL, 1998, BLOOD, V92, p645A
[10]  
Howrey RP, 1998, BLOOD, V92, p291A