Relapse of tagraxofusp treated blastic plasmacytoid dendritic cell neoplasm with loss of CD123 expression.
Rohit GulatiAsma Abu-SalahTareq SalousMehdi NassiriPublished in: Journal of hematopathology (2021)
Tagraxofusp, a CD123-based-targeted immunotherapy, was recently approved to treat blastic plasmacytoid dendritic cell neoplasm (BPDCN) with excellent response. Also, a subset of BPDCN shows resistance to tagraxofusp. These resistant cases continue to express CD123, which forms the basis of the continued utility of tagraxofusp in newer combination chemotherapies to overcome resistance in BPDCN. Herein, we report a case of an elderly male with BPDCN that achieved complete remission on initial primary treatment with tagraxofusp. However, BPDCN relapsed after 1.5 years while on treatment, with loss of CD123 expression. At relapse, the neoplasm was comprehensively immunophenotyped by flow cytometry (performed on both peripheral blood and bone marrow specimen) and by immunohistochemical evaluation of the bone marrow clot section. The neoplasm at relapse was diagnostic of BPDCN with a lack of CD123 expression. This case highlights a potential limitation of current and upcoming tagraxofusp-based multidrug therapies, at least in a subset of refractory BPDCN. We believe our report will serve as a sentinel to incite future investigations involving alternate resistance mechanisms in BDPCN.
Keyphrases
- dendritic cells
- bone marrow
- poor prognosis
- regulatory t cells
- immune response
- low grade
- flow cytometry
- peripheral blood
- mesenchymal stem cells
- acute myeloid leukemia
- acute lymphoblastic leukemia
- binding protein
- long non coding rna
- free survival
- climate change
- current status
- high grade
- multidrug resistant
- hodgkin lymphoma
- newly diagnosed
- smoking cessation
- ulcerative colitis
- community dwelling