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CD25/CD123 共表达在急性髓系白血病患者中的临床价值。

Clinical value of CD25/CD123 co-expression in acute myeloid leukemia patients.

机构信息

Hematology Unit, Clinical Pathology Department, Mansoura University Oncology Center, Mansoura University, Mansoura, Egypt.

Clinical Hematology Unit, Mansoura University Oncology Center, Mansoura University, Mansoura, Egypt.

出版信息

Cancer Biomark. 2020;29(1):9-16. doi: 10.3233/CBM-201519.

DOI:10.3233/CBM-201519
PMID:32417762
Abstract

BACKGROUND

This study aimed to assess the significance of combined expression of interleukin-2 receptor (CD25) and the interleukin-3 receptor (CD123) in acute myeloid leukemia (AML) patients.

METHODS

The expression of CD25 and CD123 on blast cells in bone marrow samples were identified by flowcytometry in 94 patients (⩽ 60 years old) with de novo acute myeloid leukemia (AML) treated at the Mansoura University Oncology Center (MUOC).

RESULTS

Of the 94 samples at diagnosis there were 17 (18.1%) CD25+/CD123+ (double positive) cases; 25 (26.6%) CD25+/CD123- (single positive); 32 (34.0%) CD25-/CD123+ (single positive) cases; 20 (21.3%). CD25-/CD123- (double negative). Most of the AML patients have double CD25+/CD123+ were significantly associated with poor and intermediate risk as compared to those associated with those in the good risk group (P= 0.005). The lowest induction of remission was recorded in AML patients have double CD25+/CD123+ expression as compared to the remaining AML patient group. Study the effect of these biomarkers on the overall survival reveal that AML patients exhibited double CD25+/CD123+ expression had significantly shorter overall survival as compared to negative ones.

CONCLUSION

Double CD25+/CD123+ co-expression in AML patients is a dismal prognostic marker and could be used as novel biomarker for risk stratification for AML patients.

摘要

背景

本研究旨在评估白细胞介素-2 受体(CD25)和白细胞介素-3 受体(CD123)在急性髓系白血病(AML)患者中的联合表达的意义。

方法

在曼苏拉大学肿瘤中心(MUOC)接受治疗的 94 例初诊急性髓系白血病(AML)患者(≤60 岁)的骨髓样本中,通过流式细胞术鉴定了骨髓原始细胞上 CD25 和 CD123 的表达。

结果

在 94 例诊断时的样本中,有 17 例(18.1%)为 CD25+/CD123+(双阳性)病例;25 例(26.6%)为 CD25+/CD123-(单阳性);32 例(34.0%)为 CD25-/CD123+(单阳性)病例;20 例(21.3%)为 CD25-/CD123-(双阴性)。大多数 AML 患者的双 CD25+/CD123+表达与不良和中等风险相关,而与良好风险组相关(P=0.005)。双 CD25+/CD123+表达的 AML 患者的缓解诱导最低,与其余 AML 患者组相比。研究这些生物标志物对总生存期的影响表明,双 CD25+/CD123+表达的 AML 患者的总生存期明显短于阴性患者。

结论

AML 患者中双 CD25+/CD123+共表达是预后不良的标志物,并可作为 AML 患者风险分层的新型生物标志物。

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