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Relapse of tagraxofusp treated blastic plasmacytoid dendritic cell neoplasm with loss of CD123 expression.
Gulati, Rohit; Abu-Salah, Asma; Salous, Tareq; Nassiri, Mehdi.
Afiliación
  • Gulati R; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, 350 W 11th Street, Room 5048, Indianapolis, IN, 46202, USA. rohitleo@gmail.com.
  • Abu-Salah A; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, 350 W 11th Street, Room 5048, Indianapolis, IN, 46202, USA.
  • Salous T; Department of Medicine- Hematology/Oncology, 535 Barnhill Drive, Indianapolis, IN, 46202, USA.
  • Nassiri M; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, 350 W 11th Street, Room 5048, Indianapolis, IN, 46202, USA.
J Hematop ; 15(1): 35-39, 2022 Mar.
Article en En | MEDLINE | ID: mdl-38358597
ABSTRACT
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.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2022 Tipo del documento: Article