COLLECTION AND TRANSPLANTATION OF PERIPHERAL-BLOOD STEM-CELLS IN VERY SMALL CHILDREN WEIGHING 20 KG OR LESS

被引:121
作者
TAKAUE, Y
KAWANO, Y
ABE, T
OKAMOTO, Y
SUZUE, T
SHIMIZU, T
SAITO, S
SATO, J
MAKIMOTO, A
NAKAGAWA, R
WATANABE, T
ITO, M
KURODA, Y
机构
关键词
D O I
10.1182/blood.V86.1.372.bloodjournal861372
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The safety and efficacy of harvesting peripheral blood hematopoietic stem cells (PBSC) were evaluated in 38 children weighing 20 kg or less, with the smallest patient weighing 7 kg. The patients had a median age of 42 months and included 26 children with acute leukemias or lymphoma and 12 with various solid tumors. A total of 81 aphereses were performed, mostly in the recovery phase of chemotherapy, with or without granulocyte colony-stimulating factor, using a CS-3000 cell separator and regular procedure no. 3. Blood was withdrawn at a mean rate of 30 mL/min (range, 17 to 46 mL/min) through a temporary radial arterial catheter (20 to 24 guage) and returned through a larger catheter in a peripheral vein. Morbidity related to PBSC harvest was low and all aphereses were completed within 3 hours. The volume of blood per kilogram processed for each apheresis ranged from 85 to 615 mL (median, 270 mL). The median number of colony-forming units-granulocyte-macrophage (CFU-GM) and CD34(+) cells collected were, respectively, 34 x 10(4)/kg and 15 x 10(6)/kg per apheresis and 126 x 10(4)/kg and 31 x 10(6)/kg per patient. Thirty-three patients (87%) required only a single apheresis to collect the minimum requirement of 10 x 10(4) CFU-GM/kg, including 28 patients (74%) from whom 30 x 10(4) CFU-GM/kg was obtained in a single apheresis. Twenty-three of the patients subsequently underwent autografts with PBSC. The median number of days required to achieve an absolute granulocyte count of 0.5 x 10(9)/L and a platelet count of 50 x 10(9)/L were, respectively, 10 (range, 6 to 15) and 14 (range, 9 to 46). The patients remained dependent on platelet transfusion support for a median of 10 days (range, 5 to 35). Thus, harvesting PBSC in very small children with active cancers is effective and safe and does not involve the risk of anesthesia or multiple invasive marrow aspirations. (C) 1995 by The American Society of Hematology.
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页码:372 / 380
页数:9
相关论文
共 26 条
[1]   PHENOTYPIC ANALYSIS AND CHARACTERIZATION OF CD34+ CELLS FROM NORMAL HUMAN BONE-MARROW, CORD-BLOOD, PERIPHERAL-BLOOD, AND MOBILIZED PERIPHERAL-BLOOD FROM PATIENTS UNDERGOING AUTOLOGOUS STEM-CELL TRANSPLANTATION [J].
BENDER, JG ;
UNVERZAGT, K ;
WALKER, DE ;
LEE, W ;
SMITH, S ;
WILLIAMS, S ;
VANEPPS, DE .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1994, 70 (01) :10-18
[2]  
BILLETT AL, 1993, AM J PEDIAT HEMATOL, V15, P162
[3]  
DEMEOCQ F, 1994, BONE MARROW TRANSPL, V13, P43
[4]   RECOVERY KINETICS AFTER CHEMOTHERAPY AND CIRCULATING MONONUCLEAR-CELLS EXPRESSING THE CD34 ANTIGEN IN PEDIATRIC CANCER-PATIENTS [J].
EMMINGER, W ;
FRITSCH, G ;
EMMINGERSCHMIDMEIER, W ;
BUCHINGER, P ;
PRINTZ, D ;
KUNDI, M ;
GADNER, H .
ANNALS OF HEMATOLOGY, 1992, 64 (04) :181-184
[5]   WHEN IS THE OPTIMUM TIME TO HARVEST PERIPHERAL-BLOOD STEM-CELLS IN CHILDREN FOLLOWING STANDARD-DOSE CHEMOTHERAPY [J].
FERNANDEZ, JM ;
SHEPHERD, V ;
MILLAR, J ;
POWLES, R ;
PINKERTON, CR .
MEDICAL AND PEDIATRIC ONCOLOGY, 1993, 21 (07) :465-469
[6]   OPTIMAL-GROWTH OF HUMAN BLOOD HEMATOPOIETIC PROGENITOR CELLS COLLECTED BY APHERESIS FOR AUTOGRAFTS [J].
HIRAO, A ;
TAKAUE, Y ;
KAWANO, Y ;
SATO, J ;
MAKIMOTO, A ;
KAWAHITO, M ;
OKAMOTO, Y ;
SAITO, S ;
SUZUE, T ;
ABE, T ;
KURODA, Y .
JOURNAL OF CLINICAL APHERESIS, 1995, 10 (01) :17-22
[7]  
KAWANO Y, 1993, EXP HEMATOL, V21, P103
[8]  
KAWANO Y, 1991, BLOOD, V77, P2118
[9]   CLINICAL COLLECTION AND USE OF PERIPHERAL-BLOOD STEM-CELLS IN PEDIATRIC-PATIENTS [J].
LASKY, LC ;
BOSTROM, B ;
SMITH, J ;
MOSS, TJ ;
RAMSAY, NKC .
TRANSPLANTATION, 1989, 47 (04) :613-616
[10]   PERIPHERAL-BLOOD STEM-CELLS USED TO AUGMENT AUTOLOGOUS BONE-MARROW TRANSPLANTATION [J].
MITCHELL, PLR ;
SHEPHERD, VB ;
PROCTOR, HM ;
DAINTON, M ;
CABRAL, SD ;
PINKERTON, CR .
ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 70 (03) :237-240