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地西他滨治疗失败的骨髓增生异常综合征患者的结局。

Outcome of patients with myelodysplastic syndrome after failure of decitabine therapy.

机构信息

Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Cancer. 2010 Aug 15;116(16):3830-4. doi: 10.1002/cncr.25247.

Abstract

BACKGROUND

The prognosis of patients with myelodysplastic syndrome (MDS) after decitabine failure is not known.

METHODS

Data from 87 patients with MDS (n=67) and chronic myelomonocytic leukemia (n=.20) after failure of decitabine regimens were reviewed.

RESULTS

After a median follow-up of 21 months from decitabine failure, 13 (15%) patients remained alive; the median survival was 4.3 months, and the estimated 12-month survival rate was 28%. The estimated 12-month survival rates were 27%, 33%, and 33%, respectively, for patients with high-risk, intermediate-2-risk, and intermediate-1-risk disease (P=.99) by the International Prognostic Scoring System. The estimated 12-month survival rates were 100%, 54%, 41%, and 18%, respectively, for patients with low-risk, intermediate-1-risk, intermediate-2-risk, and high-risk disease according to The University of Texas M. D. Anderson Cancer Center risk model (P=.01).

CONCLUSIONS

The outcome of patients after decitabine failure is poor and appears to be predictable after decitabine failure.

摘要

背景

地西他滨治疗失败后骨髓增生异常综合征(MDS)患者的预后尚不清楚。

方法

回顾了 87 例地西他滨治疗失败后(n=67)的 MDS 患者和慢性粒单核细胞白血病(n=20)的数据。

结果

从地西他滨失败到中位随访 21 个月,13 例(15%)患者仍然存活;中位生存期为 4.3 个月,估计 12 个月生存率为 28%。国际预后评分系统(IPSS)显示,高危、中危-2 级和中危-1 级疾病患者的估计 12 个月生存率分别为 27%、33%和 33%(P=.99)。根据德克萨斯大学 MD 安德森癌症中心风险模型(UT-MDACC),低危、中危-1 级、中危-2 级和高危疾病患者的估计 12 个月生存率分别为 100%、54%、41%和 18%(P=.01)。

结论

地西他滨治疗失败后患者的预后较差,而且似乎在地西他滨治疗失败后可以预测。

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