Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Maria Sklodowska-Curie Memorial Cancer Centre and Institute, Warsaw, Poland.
Eur J Haematol. 2017 Sep;99(3):255-261. doi: 10.1111/ejh.12913. Epub 2017 Jul 17.
FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) is aberration associated with poor prognosis in AML. We have analyzed the expression of MDR-1, MRP-1, and BCRP mRNA in relation to FLT3-ITD in 100 AML adult patients with normal and intermediate karyotype.
The RQ-PCR method was performed to assess the expression of MDR-1, MRP-1, and BCRP mRNA, and the results were presented as coefficients calculated using an intermediate method according to Pfaffl's rule.
According to univariate analysis, the following pretreatment variables negatively influenced disease-free survival (DFS): WBC count ≥25×10 /L (P=.037), MRP-1 mRNA ≥1.6818 (P=.028), BCRP mRNA ≥1.1892 (P=.004), FLT3-ITD (P=.005) and overall survival (OS): WBC count ≥25×10 /L (P=.031), MRP-1 mRNA ≥1.6818 (P=.01), BCRP mRNA ≥1.1892 (P=.01), FLT3-ITD (P=.001). When all prognostic variables were pooled into a multivariate model, we found that WBC count ≥25×10 /L (P=.026) and BCRP mRNA ≥1.1892 (P=.011). We observed trend in negative influence of FLT3-ITD on DFS (P=.057). BCRP mRNA ≥1.1892 (P=.035) and FLT3-ITD (P=.006) negatively, independently influenced the OS.
The high expressions of BCRP mRNA calculated with Pfaffl's rule and FLT3-ITD are independent poor risk factors in adult patients with AML and intermediate or normal karyotype.
FMS 样酪氨酸激酶 3 内部串联重复(FLT3-ITD)是与 AML 预后不良相关的异常。我们分析了 100 例核型正常和中间核型的 AML 成年患者中与 FLT3-ITD 相关的 MDR-1、MRP-1 和 BCRP mRNA 的表达。
采用 RQ-PCR 法评估 MDR-1、MRP-1 和 BCRP mRNA 的表达,结果以根据 Pfaffl 规则的中间法计算的系数表示。
根据单因素分析,以下预处理变量对无病生存(DFS)有负面影响:白细胞计数≥25×10/L(P=.037)、MRP-1 mRNA≥1.6818(P=.028)、BCRP mRNA≥1.1892(P=.004)、FLT3-ITD(P=.005)和总生存(OS):白细胞计数≥25×10/L(P=.031)、MRP-1 mRNA≥1.6818(P=.01)、BCRP mRNA≥1.1892(P=.01)、FLT3-ITD(P=.001)。当所有预后变量都被汇集到多变量模型中时,我们发现白细胞计数≥25×10/L(P=.026)和 BCRP mRNA≥1.1892(P=.011)。我们观察到 FLT3-ITD 对 DFS 的负面影响呈趋势(P=.057)。BCRP mRNA≥1.1892(P=.035)和 FLT3-ITD(P=.006)独立地对 OS 产生负面影响。
用 Pfaffl 规则计算的 BCRP mRNA 的高表达和 FLT3-ITD 是核型正常和中间核型的 AML 成年患者的独立不良预后因素。