Value of chemotherapy before allogeneic hematopoietic stem cell transplantation from an HLA-identical sibling donor for myelodysplastic syndrome

被引:92
作者
Nakai, K
Kanda, Y
Fukuhara, S
Sakamaki, H
Okamoto, S
Kodera, Y
Tanosaki, R
Takahashi, S
Matsushima, T
Atsuta, Y
Hamajima, N
Kasai, M
Kato, S
机构
[1] Tokyo Univ Hosp, Dept Cell Therapy & Transplantat Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Kansai Med Univ, Dept Internal Med 1, Osaka, Japan
[3] Tokyo Metropolitan Komagome Hosp, Div Hematol, Tokyo, Japan
[4] Keio Univ, Sch Med, Div Hematol, Tokyo 108, Japan
[5] Japanese Red Cross Nagoya First Hosp, Nagoya, Aichi, Japan
[6] Natl Canc Ctr, Tokyo, Japan
[7] Univ Tokyo, Inst Med Sci, Dept Hematol Oncol, Tokyo, Japan
[8] Gunma Univ, Grad Sch Med, Dept Med & Clin Sci, Maebashi, Gumma, Japan
[9] Nagoya Univ, Grad Sch Med, Dept Prevent Med Biostat & Med Decis Making, Nagoya, Aichi, Japan
[10] Sapporo Hokuyu Hosp, Sapporo, Hokkaido, Japan
[11] Tokai Univ, Sch Med, Hiratsuka, Kanagawa 25912, Japan
关键词
myelodysplastic syndrome; allogeneic hematopoietic; stem cell transplantation; graft-versus-host disease;
D O I
10.1038/sj.leu.2403640
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Allogeneic hematopoietic stem cell transplantation ( allo- SCT) is a curative treatment for myelodysplastic syndrome ( MDS). The object of this study was to evaluate the impact of chemotherapy before allo- SCT. We analyzed the data of 283 patients who underwent allo- SCT from an HLA- identical sibling donor for MDS that were reported to the Japan Society for Hematopoietic Cell Transplantation. The cumulative incidence of grade II - IV acute GVHD was 33%. Overall survival ( OS) at 5 and 10 years was 48.8 and 42.5%, respectively. Multivariate analyses identified karyotype, FAB classification, and the history of chemotherapy before allo- SCT as significant predictors for OS. OS at 5 years was 57% for patients who underwent allo- SCT as a primary treatment for refractory anemia with excess blasts in transformation ( RAEB- t) or secondary acute myeloid leukemia ( AML) and 54% for those who underwent allo- SCT in remission after induction chemotherapy ( P = 0.81). The proportion of patients with a poor karyotype was equivalent between the two groups ( P = 0.44). Although only a randomized controlled trial will be able to establish a definite conclusion, these results do not support the administration of induction chemotherapy for patients with RAEB- t or secondary AML before allo- SCT.
引用
收藏
页码:396 / 401
页数:6
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