Lymphocyte apheresis for chimeric antigen receptor T-cell manufacturing in children and young adults with leukemia and neuroblastoma

被引:70
作者
Ceppi, Francesco [1 ,2 ,3 ]
Rivers, Julie [1 ,4 ]
Annesley, Colleen [1 ,4 ]
Pinto, Navin [1 ,4 ]
Park, Julie R. [1 ,4 ]
Lindgren, Catherine [5 ]
Mgebroff, Stephanie [5 ]
Linn, Naomi [6 ]
Delaney, Meghan [7 ,8 ]
Gardner, Rebecca A. [1 ,4 ]
机构
[1] Seattle Childrens Hosp & Res Inst, Ctr Clin & Translat Res, Seattle, WA USA
[2] Univ Hosp Lausanne, Pediat Hematol Oncol Res Lab, Div Pediat, Dept Woman Mother Child, Lausanne, Switzerland
[3] Univ Hosp Lausanne, Pediat Hematol Oncol Unit, Div Pediat, Dept Woman Mother Child, Lausanne, Switzerland
[4] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[5] Seattle Childrens Res Inst, Ben Towne Ctr Childhood Canc Res, Seattle, WA USA
[6] Bloodworks NW, Apheresis Dept, Seattle, WA USA
[7] Childrens Natl Hlth Syst, Washington, DC USA
[8] Seattle Childrens Hosp, Dept Pathol, Seattle, WA USA
关键词
THERAPY; TUMORS;
D O I
10.1111/trf.14569
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUNDThe first step in the production of chimeric antigen receptor T cells is the collection of autologous T cells using apheresis technology. The procedure is technically challenging, because patients often have low leukocyte counts and are heavily pretreated with multiple lines of chemotherapy, marrow transplantation, and/or radiotherapy. Here, we report our experience of collecting T lymphocytes for chimeric antigen receptor T-cell manufacturing in pediatric and young adult patients with leukemia, non-Hodgkin lymphoma, or neuroblastoma. STUDY DESIGN AND METHODSApheresis procedures were performed on a COBE Spectra machine using the mononuclear cell program, with a collection target of 1 x 10(9) total mononuclear cells per kilogram. Data were collected regarding preapheresis and postapheresis blood counts, apheresis parameters, products, and adverse events. RESULTSNinety-nine patients (ages 1.3-25.7 years) and 102 apheresis events were available for analysis. Patients underwent apheresis at a variety of absolute lymphocyte cell counts, with a median absolute lymphocyte count of 944 cells/L (range, 142-6944 cells/L). Twenty-two patients (21.6%) had absolute lymphocyte counts less than 500 cells/L. The mononuclear cell target was obtained in 100% of all apheresis harvests, and chimeric antigen receptor T-cell production was possible from the majority of collections (94%). Mononuclear cell collection efficiency was 65.4%, and T-lymphocyte collection efficiency was 83.4%. Ten patients (9.8%) presented with minor adverse events during the 102 apheresis procedures, with one exception of a severe allergy. CONCLUSIONSMononuclear cell apheresis for chimeric antigen receptor T-cell therapy is well tolerated and safe, and it is possible to obtain an adequate quantity of CD3+ lymphocytes for chimeric antigen receptor T-cell manufacturing in heavily pretreated patients who have low lymphocyte counts.
引用
收藏
页码:1414 / 1420
页数:7
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