Applying molecular measurable residual disease testing in acute myeloid leukaemia

被引:4
|
作者
Krigstein, Michael [1 ,5 ]
Iland, Harry J. [2 ]
Wei, Andrew H. [3 ,4 ]
机构
[1] St Vincents Hosp, Dept Haematol, Sydney, NSW, Australia
[2] Royal Prince Alfred Hosp, Dept Haematol, Sydney, NSW, Australia
[3] Peter MacCallum Canc Ctr, Dept Haematol, Melbourne, Vic, Australia
[4] Royal Melbourne Hosp, Melbourne, Vic, Australia
[5] St Vincents Hosp, Dept Haematol, 390 Victoria St, Darlinghurst, NSW 2010, Australia
关键词
Measurable residual disease; acute myeloid leukaemia; NPM1; FLT3; clonal haematopoiesis; PROGNOSTIC VALUE; FLT3; MUTATIONS; KIT MUTATIONS; STANDARD-RISK; AML; RELAPSE; MRD; IMPACT; NPM1; TRANSPLANTATION;
D O I
10.1016/j.pathol.2022.11.003
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Molecular testing in acute myeloid leukaemia (AML) has continued to dramatically advance in recent years, facilitating the ability to detect residual disease at exponentially lower levels. With the advent of the recently updated ELN consensus recommendations, there is increasing complexity to ordering and interpreting measurable residual disease (MRD) assays in AML. We outline the technology itself in conjunction with the relevant testing timepoints, clinically significant thresholds and potential prognostic and therapeutic significance of MRD testing for the major molecular targets in AML. This practical overview should assist haematologists in incorporating molecular MRD assays routinely into their personalised AML clinical management.
引用
收藏
页码:1 / 7
页数:7
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