Clinical significance of minimal residual disease in patients with acute leukaemia undergoing haematopoietic stem cell transplantation

被引:84
作者
Campana, Dario [1 ]
Leung, Wing [2 ,3 ]
机构
[1] Natl Univ Singapore, Dept Paediat, Yong Loo Lin Sch Med, Singapore 117599, Singapore
[2] Univ Tennessee, Ctr Hlth Sci, Dept Bone Marrow Transplantat & Cellular Therapy, St Jude Childrens Res Hosp, Memphis, TN 38163 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Pediat, Coll Med, Memphis, TN 38163 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
acute lymphoblastic leukaemia; acute myeloid leukaemia; minimal residual disease; haematopoietic stem cell transplantation; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; ALLOGENEIC BONE-MARROW; NATURAL-KILLER-CELLS; CORD BLOOD TRANSPLANTATION; TIME QUANTITATIVE PCR; WT1; GENE-EXPRESSION; IN-VITRO GROWTH; PROGNOSTIC-SIGNIFICANCE; FLOW-CYTOMETRY;
D O I
10.1111/bjh.12358
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In patients with acute leukaemia, the relative risk of relapse influences the choice between chemotherapy and haematopoietic stem cell transplantation (HSCT). The demonstration that minimal residual disease (MRD) is the strongest overall prognostic indicator and can identify patients who are unlikely to be cured by standard chemotherapy has added a powerful new factor to consider when making this decision. There is substantial data indicating that the likelihood of relapse after transplant is directly correlated with levels of MRD before transplant. This knowledge can be used to adjust the timing of HSCT, and guide the selection of donor, conditioning regimen, and post-HSCT strategies to maximize the graft-versus-leukaemia effect. Because MRD emerging post-transplant carries a dire prognosis, its detection can trigger withdrawal of immunosuppression, additional cellular and molecular therapies, or preparations for a second HSCT. Although it is not yet clear whether any of these actions will significantly improve outcome, it is likely that they will be most effective for patients with a relatively low tumour burden, who can be identified only through MRD testing. In this article, we review the clinical significance of MRD in the context of autologous and allogeneic HSCT.
引用
收藏
页码:147 / 161
页数:15
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