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Prognostic and therapeutic role of CLEC12A in acute myeloid leukemia.
Morsink, Linde M; Walter, Roland B; Ossenkoppele, Gert J.
Afiliação
  • Morsink LM; Department of Hematology, Amsterdam UMC, VU University Medical Center, Amsterdam, the Netherlands. Electronic address: l.morsink@vumc.nl.
  • Walter RB; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Medicine, Division of Hematology, University of Washington, Seattle, WA, USA; Department of Epidemiology, University of Washington, Seattle, WA, USA.
  • Ossenkoppele GJ; Department of Hematology, Amsterdam UMC, VU University Medical Center, Amsterdam, the Netherlands.
Blood Rev ; 34: 26-33, 2019 03.
Article em En | MEDLINE | ID: mdl-30401586
CLEC12A has recently been identified as an antigen, expressed on leukemic stem cells and leukemic blasts. Given the fact that this expression profile seems stable throughout diagnosis, treatment and relapse on leukemic blasts and leukemic stem cells, CLEC12A can be considered a highly potent and reliable marker for the detection of measurable residual disease and therefore applicable for risk stratification and prognostication in AML. Low CLEC12A expression on leukemic blasts seems to be independently associated with lower likelihood of achieving complete remission after 1 cycle of induction chemotherapy, shorter event free survival, as well as overall survival, indicating potential prognostic properties of CLEC12A expression itself. Lack of expression on the normal hematopoietic stem and progenitor cells, in contrast to CD123 and CD33, might result in less toxicity regarding cytopenias, making CLEC12A an interesting target for innovating immunotherapies, including monoclonal and bispecific antibodies, antibody-drug conjugates and CAR-T cells therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Mitogênicos / Leucemia Mieloide Aguda / Biomarcadores Tumorais / Lectinas Tipo C Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Mitogênicos / Leucemia Mieloide Aguda / Biomarcadores Tumorais / Lectinas Tipo C Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article