Conditioning Regimen of 5-Day Decitabine Administration for Allogeneic Stem Cell Transplantation in Patients with Myelodysplastic Syndrome and Myeloproliferative Neoplasms

被引:34
|
作者
Cao, Yi-Geng
He, Yi
Zhang, Su-Dong
Liu, Zi-Xian
Zhai, Wei-Hua
Ma, Qiao-Ling
Pang, Ai-Ming
Wei, Jia-Ling
Yang, Dong-Ling
Huang, Yong
Feng, Si-Zhou
Jiang, Er-Lie [1 ,2 ]
Han, Ming-Zhe
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Ctr Hematopoiet Stem Cell Transplantat, Inst Hematol, 288 Nanjing Rd, Tianjin 300200, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Blood Dis Hosp, 288 Nanjing Rd, Tianjin 300200, Peoples R China
基金
中国国家自然科学基金;
关键词
Decitabine; Allogeneic hematopoietic stem cell transplantation; Myeloablative conditioning regimen; Myelodysplastic syndromes; Myelodysplastic/myeloproliferative neoplasms; ACUTE MYELOID-LEUKEMIA; CORD BLOOD TRANSPLANTATION; CANCER TESTIS ANTIGEN; WORKING GROUP; 5-AZA-2'-DEOXYCYTIDINE; HAPLOTYPES; INDUCTION; CRITERIA; THERAPY; PHASE-1;
D O I
10.1016/j.bbmt.2019.09.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment for patients with myelodysplastic syndromes (MDS) and myelodysplastic/myeloproliferative neoplasms (MDS/MPN). However, post-HSCT relapse remains a major cause of treatment failure. Here we assessed the efficacy of a new conditioning regimen comprising decitabine (Dec), busulfan (Bu), cyclophosphamide (Cy), fludarabine (Flu), and cytarabirie (Ara-c) for allo-HSCT in patients with MDS and MDS/MPN. A total of 48 patients were enrolled, including 44 with MDS and 4 with chronic myelomonocytic leukemia (CMML). Patients received Dec 20 mg/m(2)/day on days -9 to -5, combined with a Bu/Cy/Flu/Ara-c-modified preparative regimen. At a median follow-up of 522 days (range, 15 to 1313 days), the overall survival (OS) was 86%, relapse incidence was 12%, and nonrelapse mortality was 12%. The incidence of severe acute (grade III-IV) graft-versus-host disease (GVHD) was 23% and that of chronic GVHD was 15%. At 2 years, OS was 74% and 86%, respectively for high-risk and very-high-risk patients with MDS. Survival was promising in patients with poor-risk gene mutations, such as TP53 and ASXL1 (88%), and in those with >= 3 gene mutations (79%). Results of immunomonitoring studies revealed that proper natural killer cells made essential contributions to these favorable clinical outcomes. Overall, this new regimen was associated with a low relapse rate, low incidence and severity of GVHD, and satisfactory survival in allo-HSCT recipients with MDS and MDS/MPN. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
引用
收藏
页码:285 / 291
页数:7
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