Efficacy and toxicity of decitabine versus CHG regimen (low-dose cytarabine, homoharringtonine and granulocyte colony-stimulating factor) in patients with higher risk myelodysplastic syndrome: a retrospective study

被引:8
|
作者
Wu, Lingyun [1 ]
Li, Xiao [1 ]
Chang, Chunkang [1 ]
Xu, Feng [1 ]
He, Qi [1 ]
Wu, Dong [1 ]
Zhang, Zheng [1 ]
Su, Jiying [1 ]
Zhou, Liyu [1 ]
Song, Luxi [1 ]
Chao, Xiao [1 ]
Zhao, Youshan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Hematol, Affiliated Peoples Hosp 6, 600 Yishan Rd, Shanghai 200233, Peoples R China
关键词
Cytarabine; decitabine; granulocyte colony-stimulating factor (G-CSF); homoharringtonine; myelodysplastic syndromes; MYELOID-LEUKEMIA; PHASE-III; MULTICENTER; DISEASE; MDS; CLASSIFICATION; CHEMOTHERAPY; SYSTEM;
D O I
10.3109/10428194.2015.1096351
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Decitabine and CHG regimen (low-dose cytarabine and homoharringtonine with G-CSF) have been used for treating higher risk myelodysplastic syndrome (MDS). In this study, we retrospectively compared the efficacy and toxicity of the two regimens in 132 MDS patients. Complete remission (CR) was not significantly different between the groups (27.1% with decitabine vs. 30.6% with CHG, p=0.657). The CR rate with decitabine (58.8%) was significantly higher than that with CHG (7.7%) (p=0.007) among the patients with poor karyotypes. Five of 23 (21.7%) patients who failed to respond to decitabine achieved CR with CHG, while one of two patients achieved CR with decitabine after failure with CHG. Overall and relapse-free survival were not different between the groups. In conclusion, both decitabine and CHG regimen are effective for higher risk MDS; there is no cross resistance between the regimens. Decitabine might be a better choice for patients with poor karyotypes.
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页码:1367 / 1374
页数:8
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