Novel Biomarkers for Outcome After Allogeneic Hematopoietic Stem Cell Transplantation

被引:11
作者
Chen, Sophia [1 ,2 ]
Zeiser, Robert [2 ,3 ,4 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dept Immunol, 1275 York Ave, New York, NY 10021 USA
[2] Univ Freiburg, Dept Med 1, Med Ctr, Fac Med, Freiburg, Germany
[3] German Canc Consortium DKTK, Partner Site Freiburg, Freiburg, Germany
[4] Univ Freiburg, Ctr Integrat Biol Signalling Studies, Signalling Res Ctr BIOSS, Freiburg, Germany
[5] Univ Freiburg, Ctr Integrat Biol Signalling Studies, Signalling Res Ctr CIBSS, Freiburg, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
基金
欧洲研究理事会;
关键词
biomarker; GVHD; steroid-refractory graft-vs; -host disease; immune cells; relapse; minimal residual disease; VERSUS-HOST-DISEASE; MINIMAL RESIDUAL DISEASE; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; SERUM CYTOKINE LEVELS; PLASMA BIOMARKERS; ACUTE GVHD; FECAL CALPROTECTIN; TRANSCRIPT LEVELS; PROGNOSTIC-FACTOR;
D O I
10.3389/fimmu.2020.01854
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a well-established curative treatment for various malignant hematological diseases. However, its clinical success is substantially limited by major complications including graft-vs.-host disease (GVHD) and relapse of the underlying disease. Although these complications are known to lead to significant morbidity and mortality, standardized pathways for risk stratification of patients undergoing allo-HSCT are lacking. Recent advances in the development of diagnostic and prognostic tools have allowed the identification of biomarkers in order to predict outcome after allo-HSCT. This review will provide a summary of clinically relevant biomarkers that have been studied to predict the development of acute GVHD, the responsiveness of affected patients to immunosuppressive treatment and the risk of non-relapse mortality. Furthermore, biomarkers associated with increased risk of relapse and subsequent mortality will be discussed.
引用
收藏
页数:15
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