Prognostic and therapeutic role of CLEC12A in acute myeloid leukemia

被引:40
作者
Morsink, Linde M. [1 ]
Walter, Roland B. [2 ,3 ,4 ]
Ossenkoppele, Gert J. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Amsterdam UMC, Dept Hematol, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
[3] Univ Washington, Dept Med, Div Hematol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
关键词
Acute myeloid leukemia; Antibody; Antibody-drug conjugate; Bispecific antibody; BiTE; CLEC12A; Chimeric antigen receptor; CLL-1; Immunotherapy; MINIMAL RESIDUAL DISEASE; T-CELL THERAPY; LECTIN-LIKE MOLECULE-1; GEMTUZUMAB OZOGAMICIN; STEM-CELLS; FLOW-CYTOMETRY; MICL CLEC12A; RECEPTOR; AML; EXPRESSION;
D O I
10.1016/j.blre.2018.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:26 / 33
页数:8
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