Liu Hui
Department of Hematology, 3201 Hospital of Xi'an Jiaotong University Health Science Center, Hanzhong, People's Republic of China.
Hematology. 2023 Dec;28(1):2161194. doi: 10.1080/16078454.2022.2161194.
SET domain containing protein 2 (SETD2) involves in the progression and development of chemotherapy resistance in acute myeloid leukemia (AML). Hence, this study aimed to investigate the relationship of SETD2 expression with disease risk, features, treatment response, and survival profile in AML.
One-hundred and sixty primary AML patients were retrospectively analyzed. Their bone marrow (BM) samples before and after induction therapy were retrieved for SETD2 detection by RT-qPCR. Moreover, SETD2 expression in BM samples of 20 disease controls (DCs) were also determined.
SETD2 expression was downregulated in AML patients compared to DCs (< 0.001). Higher SETD2 expression related to white blood cells ≤10 × 10/L despite not reaching statistical significance (= 0.062). One-hundred and nineteen (74.4%) AML patients achieved complete response (CR), while the remaining 41 (25.6%) did not achieve that. Furthermore, increased SETD2 expression was associated with CR achievement (= 0.015). Survival analyses displayed that SETD2 high (vs. low) was related to prolonged event-free survival (EFS) (= 0.001) and overall survival (OS) (= 0.021). Moreover, increased SETD2 quartile was correlated with favorable EFS (= 0.004) and OS (= 0.042). After adjustment using multivariate Cox's regression analysis, higher SETD2 quartile was independently related to prolonged EFS [hazard ratio (HR): 0.766, = 0.013] and OS (HR: 0.669, = 0.013). It was also noticed that SETD2 expression was elevated during the induction therapy (< 0.001).
Detection of SETD2 may assist in estimating treatment response and survival profile in AML patients.
含SET结构域蛋白2(SETD2)参与急性髓系白血病(AML)化疗耐药的进展与发展。因此,本研究旨在探讨SETD2表达与AML疾病风险、特征、治疗反应及生存情况之间的关系。
回顾性分析160例原发性AML患者。收集其诱导治疗前后的骨髓(BM)样本,采用RT-qPCR检测SETD2。此外,还测定了20例疾病对照(DCs)BM样本中的SETD2表达。
与DCs相比,AML患者中SETD2表达下调(<0.001)。较高的SETD2表达与白细胞≤10×10⁹/L相关,尽管未达到统计学意义(P=0.062)。119例(74.4%)AML患者达到完全缓解(CR),其余41例(25.6%)未达到。此外,SETD2表达增加与CR的实现相关(P=0.015)。生存分析显示,SETD2高表达(与低表达相比)与无事件生存期(EFS)延长(P=0.001)和总生存期(OS)延长(P=0.021)相关。此外,SETD2四分位数增加与良好的EFS(P=0.004)和OS(P=0.042)相关。使用多变量Cox回归分析进行调整后,较高的SETD2四分位数与EFS延长独立相关[风险比(HR):0.766,P=0.013]和OS(HR:0.669,P=0.013)。还注意到诱导治疗期间SETD2表达升高(<0.001)。
检测SETD2可能有助于评估AML患者的治疗反应和生存情况。