Myeloid/lymphoid neoplasms with FLT3 rearrangement.
Guilin TangWayne TamNicholas J ShortPrithviraj BoseDavid WuStephanie N HurwitzAdam BaggHeesun Joyce RogersEric D HsiAndres E QuesadaWei WangRoberto N MirandaCarlos E Bueso-RamosL Jeffrey MedeirosValentina NardiRobert P HasserjianDaniel A ArberAttilio OraziKathryn FoucarSa A WangPublished in: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc (2021)
Myeloid/lymphoid neoplasms (M/LN) with 13q12/FLT3 rearrangement have been suggested as candidates for possible inclusion in the World Health Organization classification group of M/LN with eosinophilia (M/LN-eo). We report 12 patients with confirmed FLT3 rearrangement, six with t(12;13)/ETV6-FLT3; one with ins(13;22)/BCR-FLT3; and five with an unconfirmed partner gene located on chromosome bands 2p16, 3q27, 5q15, 5q35, and 7q36. Disease presentations were heterogeneous, including lymphoblastic leukemia/lymphoma, myeloid sarcoma, chronic eosinophilic leukemia, chronic myelomonocytic leukemia, and myelodysplastic syndrome. However, some common features were observed, such as extramedullary involvement (n = 7, 58%), associated eosinophilia in blood, bone marrow, or tissue (n = 8, 67%), multilineage involvement, either as biphasic myeloid/lymphoid neoplasms (n = 2) or mixed phenotype acute leukemia (n = 2). Mutations were detected in 4/8 (50%) patients by next-generation sequencing. None (0/10) had FLT3 or KIT mutations. Eleven patients received disease-based chemotherapy or hypomethylating agents, three received FLT3 inhibitors, and five patients proceeded to hematopoietic stem cell transplant. Together with a review of 16 cases published in the literature, it is apparent that M/LNs with FLT3 rearrangement show disease features reminiscent of members in the category of M/LN-eo with PDGFRA, PDGFRB, FGFR1, and PCM1/JAK2 rearrangement, characterized by a specific gene rearrangement, frequent eosinophilia, multi-lineage involvement and therapeutic benefit from kinase inhibitors.
Keyphrases
- acute myeloid leukemia
- bone marrow
- tyrosine kinase
- end stage renal disease
- chronic kidney disease
- ejection fraction
- squamous cell carcinoma
- dendritic cells
- systematic review
- copy number
- randomized controlled trial
- prognostic factors
- machine learning
- hepatitis c virus
- patient reported outcomes
- gene expression
- single cell
- computed tomography
- human immunodeficiency virus
- circulating tumor cells
- cell free
- contrast enhanced