Literature DB >> 29797659

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

Matthew J Oberley1, Paul S Gaynon2, Deepa Bhojwani2, Michael A Pulsipher2, Rebecca A Gardner3,4, Matthew C Hiemenz1, Jianling Ji1, Jennifer Han1, Maurice R G O'Gorman1, Alan S Wayne2, Gordana Raca1.   

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.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  AML; B-ALL; CAR-T; leukemia

Mesh:

Substances:

Year:  2018        PMID: 29797659     DOI: 10.1002/pbc.27265

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


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