Hypomethylating Agents for Relapse after Allogeneic Hematopoietic Cell Transplantation in Myeloid Malignancies: A Case Series and Review of the Literature

被引:1
|
作者
Im, Annie [1 ,2 ]
Raptis, Anastasios [1 ,2 ]
Hou, Jing-Zhou [1 ,2 ]
Tompkins, Cheryl [1 ,2 ]
Winfield, Melissa [1 ,2 ]
Guay, Mary [3 ]
Boyiadzis, Michael [1 ,2 ]
Agha, Mounzer [1 ,2 ]
机构
[1] Univ Pittsburgh, Med Ctr, Div Hematol Oncol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
[3] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD USA
关键词
Stem cell transplantation; Acute myeloid leukemia; Myelodysplastic syndrome; DNA methylation; Graft-versus-tumor effect; DONOR LYMPHOCYTE INFUSIONS; LOW-DOSE AZACITIDINE; REGULATORY T-CELLS; SALVAGE THERAPY; LEUKEMIA; AML; EXPRESSION; MDS;
D O I
10.1159/000444118
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Relapse is a leading cause of mortality after allogeneic hematopoietic cell transplantation (HCT). Hypomethylating agents (HMAs) have immunomodulatory properties, including augmenting tumor antigen presentation that may enhance the graft-versus-leukemia effect. Moreover, inhibitory effects on T-cell activation and cytokine production may lead to a lower incidence of graft-versus-host disease (GVHD). Our aim was to describe outcomes in patients treated with HMAs for relapse after HCT. Methods: Subjects were retrospectively identified as patients with relapse or loss of donor chimerism after HCT for myeloid malignancies treated with HMAs at the University of Pittsburgh. Results: Thirteen patients were identified, with a median age of 57 years and a median time to relapse of 98 days. Nine of 12 (75%) evaluable patients had a complete remission (CR). Grade I-IV acute GVHD involving the liver occurred in 6 patients. Cases of acute liver GVHD were diagnosed clinically based on the elevation of liver function tests. The median survival was 14.3 months from the time of relapse. Conclusion: HMAs for relapse after HCT can be effective in inducing a CR. This may be due to epigenetic changes and immunomodulatory effects that enhance the graft-versus-leukemia effect. There may be a risk of GVHD, and further exploration into pathophysiology and predisposing factors are warranted. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:232 / 237
页数:6
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