[Long-term hypomethylating agents in patients with myelodysplastic syndromes: a multi-center retrospective study].

Q3 Medicine
X Z Liu, S J Zhou, J Huang, C F Zhao, L X Jiang, Y D Zhang, C Mei, L Y Ma, X P Zhou, Y P Shao, G Q Wu, X B Xiao, R X Yao, X H Du, T L Hu, S X Qian, Y Li, X F Yan, L Huang, M L Wang, J P Fu, L H Shou, W H Jiang, W M Jin, L J Li, J Le, W J Luo, Y Zhang, X J Zhou, H Zhang, X H Lang, M Zhou, J Jin, H F Jiang, J Zhang, G F Ouyang, H Y Tong
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引用次数: 0

Abstract

Objective: To evaluate the efficacy and safety of hypomethylating agents (HMA) in patients with myelodysplastic syndromes (MDS) . Methods: A total of 409 MDS patients from 45 hospitals in Zhejiang province who received at least four consecutive cycles of HMA monotherapy as initial therapy were enrolled to evaluate the efficacy and safety of HMA. Mann-Whitney U or Chi-square tests were used to compare the differences in the clinical data. Logistic regression and Cox regression were used to analyze the factors affecting efficacy and survival. Kaplan-Meier was used for survival analysis. Results: Patients received HMA treatment for a median of 6 cycles (range, 4-25 cycles) . The complete remission (CR) rate was 33.98% and the overall response rate (ORR) was 77.02%. Multivariate analysis revealed that complex karyotype (P=0.02, OR=0.39, 95%CI 0.18-0.84) was an independent favorable factor for CR rate. TP53 mutation (P=0.02, OR=0.22, 95%CI 0.06-0.77) was a predictive factor for a higher ORR. The median OS for the HMA-treated patients was 25.67 (95%CI 21.14-30.19) months. HMA response (P=0.036, HR=0.47, 95%CI 0.23-0.95) was an independent favorable prognostic factor, whereas complex karyotype (P=0.024, HR=2.14, 95%CI 1.10-4.15) , leukemia transformation (P<0.001, HR=2.839, 95%CI 1.64-4.92) , and TP53 mutation (P=0.012, HR=2.19, 95%CI 1.19-4.07) were independent adverse prognostic factors. There was no significant difference in efficacy and survival between the reduced and standard doses of HMA. The CR rate and ORR of MDS patients treated with decitabine and azacitidine were not significantly different. The median OS of patients treated with decitabine was longer compared with that of patients treated with azacitidine (29.53 months vs 20.17 months, P=0.007) . The incidence of bone marrow suppression and pneumonia in the decitabine group was higher compared with that in the azacitidine group. Conclusion: Continuous and regular use of appropriate doses of hypomethylating agents may benefit MDS patients to the greatest extent if it is tolerated.

[骨髓增生异常综合征患者长期服用低甲基化药物:一项多中心回顾性研究]。
目的评估低甲基化药物(HMA)对骨髓增生异常综合征(MDS)患者的疗效和安全性。方法:共纳入浙江省 45 家医院的 409 例 MDS 患者,这些患者均接受过至少 4 个连续周期的 HMA 单药初始治疗,以评估 HMA 的疗效和安全性。采用 Mann-Whitney U 或 Chi-square 检验比较临床数据的差异。采用 Logistic 回归和 Cox 回归分析影响疗效和生存率的因素。Kaplan-Meier 用于生存分析。结果患者接受 HMA 治疗的中位数为 6 个周期(范围为 4-25 个周期)。完全缓解率(CR)为 33.98%,总反应率(ORR)为 77.02%。多变量分析显示,复杂核型(P=0.02,OR=0.39,95%CI 0.18-0.84)是CR率的独立有利因素。TP53突变(P=0.02,OR=0.22,95%CI 0.06-0.77)是较高ORR的预测因素。HMA治疗患者的中位OS为25.67(95%CI 21.14-30.19)个月。HMA反应(P=0.036,HR=0.47,95%CI 0.23-0.95)是独立的有利预后因素,而复杂核型(P=0.024,HR=2.14,95%CI 1.10-4.15)、白血病转化(PHR=2.839,95%CI 1.64-4.92)和TP53突变(P=0.012,HR=2.19,95%CI 1.19-4.07)是独立的不利预后因素。减量和标准剂量的HMA在疗效和生存率方面无明显差异。接受地西他滨和阿扎胞苷治疗的MDS患者的CR率和ORR无明显差异。与阿扎胞苷相比,地西他滨治疗患者的中位生存期更长(29.53个月 vs 20.17个月,P=0.007)。与阿扎胞苷组相比,地西他滨组骨髓抑制和肺炎的发生率更高。结论如果能够耐受,持续、规律地使用适当剂量的低甲基化药物可使 MDS 患者最大程度地获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
100
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