Hematology Unit, Clinical Pathology Department, Mansoura University Oncology Center, Mansoura University, Mansoura, Egypt.
Clinical Hematology Unit, Mansoura University Oncology Center, Mansoura University, Mansoura, Egypt.
Cancer Biomark. 2020;29(1):9-16. doi: 10.3233/CBM-201519.
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.
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).
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.
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.
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。
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。
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。
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。