Zeng Hui, Yin Ling-Di, Li Ping, Yuan Yan-Hui, Guan Chao-Yang, Xie Ting, Zhang Qi-Guo
a Department of Hematology , Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School , Nanjing 210008 , China.
b First School of Clinical Medicine, Nanjing Medical University , Nanjing 210029 , China.
Hematology. 2016 Oct;21(9):513-9. doi: 10.1080/10245332.2016.1150410. Epub 2016 Mar 31.
The increased flow cytometry enumeration of peripheral blood circulating CD34+ cells in patients with acute leukemia has been found in our previous work. In this study, we also demonstrated that acute promyelocytic leukemia (APL) patients not only had elevated CD34+ cell count, but also had some clinical features.
Fifty APL patients and 19 healthy volunteers were included in the study. The enumeration of circulating CD34+ cells, cytogenetic subgroup, immunophenotype analysis, and leukemic-related gene mutation detection were performed.
Some APL patients with higher count of CD34+ cells (≤10 × 10(6)/l) usually possessed one or more poor prognostic factors (higher WBCs count, PML/RARa gene complex fusion, chemotherapy-related APL, normal karyotype/complex karyotype abnormalities, CD56/CD34 antigen positive expression, FLT3-ITD positive mutation, myelofibrosis, and marrow necrosis). A cut-off value of 10 × 10(6)/l CD34+ cells may have the power to distinguish APL patients with above adverse clinical prognostic factor from other APL subjects.
The circulating CD34+ cell count appears to increase in some APL patients and a higher CD34+ cell count may be indicative of inferior survival and serve as an adverse biomarker for APL.
在我们之前的研究中发现,急性白血病患者外周血循环CD34+细胞的流式细胞术计数增加。在本研究中,我们还证明急性早幼粒细胞白血病(APL)患者不仅CD34+细胞计数升高,而且具有一些临床特征。
本研究纳入了50例APL患者和19名健康志愿者。进行了循环CD34+细胞计数、细胞遗传学亚组分析、免疫表型分析和白血病相关基因突变检测。
一些CD34+细胞计数较高(≤10×10⁶/l)的APL患者通常具有一个或多个不良预后因素(白细胞计数较高、PML/RARa基因复合融合、化疗相关APL、正常核型/复杂核型异常、CD56/CD34抗原阳性表达、FLT3-ITD阳性突变、骨髓纤维化和骨髓坏死)。10×10⁶/l的CD34+细胞临界值可能有助于将具有上述不良临床预后因素的APL患者与其他APL患者区分开来。
一些APL患者的循环CD34+细胞计数似乎增加,较高的CD34+细胞计数可能预示较差的生存率,并可作为APL的不良生物标志物。