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Myeloid lineage switch following chimeric antigen receptor T-cell therapy in a patient with TCF3-ZNF384 fusion-positive B-lymphoblastic leukemia.

Authors :
Oberley MJ
Gaynon PS
Bhojwani D
Pulsipher MA
Gardner RA
Hiemenz MC
Ji J
Han J
O'Gorman MRG
Wayne AS
Raca G
Source :
Pediatric blood & cancer [Pediatr Blood Cancer] 2018 Sep; Vol. 65 (9), pp. e27265. Date of Electronic Publication: 2018 May 24.
Publication Year :
2018

Abstract

A pediatric patient diagnosed initially with B-lymphoblastic leukemia (B-ALL) relapsed with lineage switch to acute myeloid leukemia (AML) after chimeric antigen receptor T-cell (CAR-T) therapy and hematopoietic stem cell transplant. A TCF3-ZNF384 fusion was identified at diagnosis, persisted through B-ALL relapse, and was also present in the AML relapse cell population. ZNF384-rearrangements define a molecular subtype of B-ALL characterized by a pro-B-cell immunophenotype; furthermore, ZNF384-rearrangements are prevalent in mixed-phenotype acute leukemias. Lineage switch following CAR-T therapy has been described in patients with KMT2A (mixed lineage leukemia) rearrangements, but not previously in any patient with ZNF384 fusion.<br /> (© 2018 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1545-5017
Volume :
65
Issue :
9
Database :
MEDLINE
Journal :
Pediatric blood & cancer
Publication Type :
Academic Journal
Accession number :
29797659
Full Text :
https://doi.org/10.1002/pbc.27265