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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.
- 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.)
- Subjects :
- Basic Helix-Loop-Helix Transcription Factors genetics
Cell Lineage
Combined Modality Therapy
Cord Blood Stem Cell Transplantation
Fatal Outcome
Hematopoietic Stem Cell Transplantation
Humans
Infant
Leukemia, Myeloid, Acute genetics
Male
Oncogene Proteins, Fusion genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma therapy
Salvage Therapy
Trans-Activators genetics
Immunotherapy, Adoptive methods
Leukemia, Myeloid, Acute etiology
Myeloid Cells pathology
Precursor Cell Lymphoblastic Leukemia-Lymphoma pathology
Receptors, Chimeric Antigen immunology
T-Lymphocyte Subsets immunology
Subjects
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