[急性髓性白血病患者血清 CysC、β2-MG 与去甲基化疗法疗效的关系]

Q4 Medicine
Cai-Hong Zhang, Rui-Jun Su, Bin-Tao Huang, Zhi-Ling Wang
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引用次数: 0

摘要

研究目的分析急性髓性白血病(AML)患者血清胱抑素C(CysC)、β2-微球蛋白(β2-MG)与去甲基化治疗疗效的关系:对内蒙古医科大学附属医院2019年2月至2022年1月收治的98例AML患者进行了前瞻性队列研究。所有患者均接受地西他滨(DAC)+HAG方案治疗,28天为一疗程,治疗3-4个疗程。每个疗程结束后,对患者的治疗效果进行评估,达到完全缓解(CR)的患者转入巩固治疗,疗程结束时未达到CR的患者视为治疗失败。治疗前的检查项目包括血常规、血清 CysC 和 β2-MG,并收集患者的一般临床资料。根据统计结果,采用Logistic回归模型分析急性髓细胞白血病患者血清CysC、β2-MG与去甲基化治疗疗效的关系。绘制ROC曲线,用曲线下面积(AUC)评价血清CysC、β2-MG对AML患者去甲基化治疗的预测效果:98例急性髓细胞白血病患者中,5例在治疗期间被排除,93例最终完成了化疗疗程。其中,23例患者在首次诱导化疗(1-2疗程)后达到CR,11例患者在再次诱导化疗(3-4疗程)后达到CR。去甲基化治疗的成功率为 36.56%(34/93)。与治疗成功组患者相比,治疗失败组患者的中危和不良风险比例较高,血小板(PLT)和血红蛋白(Hb)水平较低,血清CysC和β2-MG表达水平较高,均有统计学意义(P<0.05)。逻辑回归分析显示,血清CysC、β2-MG的高表达和不良风险是AML患者去甲基化治疗失败的独立危险因素(OR>1,P<0.05)。ROC曲线显示,血清CysC、β2-MG单独或合并预测AML患者去甲基化疗效的AUC值分别为0.788、0.785和0.834:AML患者去甲基化治疗失败与血清CysC和β2-MG的高表达有关,治疗前检测血清CysC和β2-MG可预测AML患者去甲基化治疗失败的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The Relationship Between Serum CysC, β2-MG and the Efficacy of Demethylation Therapy in Patients with Acute Myeloid leukemia].

Objective: To analyze the relationship between serum cystatin C (CysC), β2-microglobulin (β2-MG) and the efficacy of demethylation therapy in patients with acute myeloid leukemia (AML).

Methods: A prospective cohort study was conducted on 98 AML patients admitted to the Affiliated Hospital of Inner Mongolia Medical University from February 2019 to January 2022. All patients were treated with decitabine (DAC) + HAG regimen, 28 days as a course and treated for 3-4 courses. At the end of each course of treatment, the treatment effect of the patients was evaluated, and the patients who achieved complete remission (CR) transferred to consolidation therapy, while the patients who did not reach CR at the end of the course of treatment were considered as treatment failure. The examination items before treatment include routine blood parameters, serum CysC, and β2-MG, and general clinical data of the patients were collected. According to the statistical results, logistic regression model was used to analyze the relationship between serum CysC, β2-MG and the efficacy of demethylation therapy in AML patients. The ROC curves were drawn, and the predictive efficacy of serum CysC, β2-MG on demethylation therapy in AML patients was evaluated by the area under the curve (AUC).

Results: Of the 98 AML patients enrolled in the study, 5 cases were excluded during the treatment period, and 93 cases finally completed the chemotherapy courses. Among them, 23 patients achieved CR after the initial induction chemotherapy (course 1-2), and 11 patients achieved CR after the re-induction chemotherapy (course 3-4). The success rate of demethylation therapy was 36.56 % (34/93). Compared with the patients in treatment success group, patients in treatment failure group had a higher proportion of intermediate- and adverse-risk, lower levels of platelet (PLT) and hemoglobin (Hb), and higher expression levels of serum CysC and β2-MG, all of which were statistically significant (P < 0.05). Logistic regression analysis showed that high expression of serum CysC, β2-MG and adverse-risk were independent risk factors for failure of demethylation treatment in AML patients (OR >1, P < 0.05). The ROC curves showed that the AUC values of serum CysC, β2-MG alone and combined in predicting the efficacy of demethylation therapy in AML patients were 0.788, 0.785 and 0.834, respectively.

Conclusion: The failure of demethylation therapy in AML patients is related to the high expression of serum CysC and β2-MG, and detection of serum CysC and β2-MG before treatment can predict the risk of demethylation therapy failure in AML patients.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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