Kannan Narasimhapriyan, Dass Jasmita, Parikh Himil, Tiwari Sarjana, Viswanathan Ganesh Kumar, Aggarwal Mukul, Kumar Pradeep, Dhawan Rishi, Seth Tulika, Tyagi Seema, Mahapatra Manoranjan
Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.
Present Address: Department of Pathology, JIPMER, Puducherry, India.
Indian J Hematol Blood Transfus. 2024 Jul;40(3):437-442. doi: 10.1007/s12288-023-01719-1. Epub 2023 Nov 30.
To evaluate the utility of CD43 and CD200 in differentiating chronic lymphocytic leukemia (CLL) from other mature B-cell neoplasms. This was a cross-sectional study on patients diagnosed with B-cell neoplasms on flowcytometry. The median fluorescence intensity (MFI) of CD43, CD200 expressing neoplastic B-cells were compared between the CLL and non-CLL B-cell neoplasms followed by receiver operating characreristic curve (ROC) analysis. In addition, the sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of CD43 and CD200 in diagnosing CLL were analysed. A total of 137 patients were included. The CLL group consisted 87 patients and non-CLL group consisted 50 patients. The Mann-Whitney U test showed significant CD43 expression (U = 997.5, Z= - 5.265, < 0.001) and CD200 expression (U = 932.0, Z = - 5.5, < 0.01) in CLL patients compared to non-CLL patients. The area under the curve were 0.771 and 0.786 for MFI of CD43 and CD200 in differentiating CLL from non-CLL group respectively. The optimal cut-off of MFI for CD43 and CD200 were 1323 and 1775 respectively. The sensitivity, specificity, PPV and NPV of CD43 in diagnosing CLL cases were 97.7%, 66%, 83.3% and 94.2% respectively. The sensitivity, specificity, PPV and NPV of CD200 in diagnosing CLL cases were 100%, 32%, 71.9% and 100% respectively. CD43 and CD200 are useful markers in differentiating CLL from other mature B-cell neoplasms with higher MFI expression of both markers found in CLL.
评估CD43和CD200在鉴别慢性淋巴细胞白血病(CLL)与其他成熟B细胞肿瘤中的作用。这是一项针对通过流式细胞术诊断为B细胞肿瘤患者的横断面研究。比较了CLL和非CLL B细胞肿瘤中表达CD43、CD200的肿瘤性B细胞的中位荧光强度(MFI),随后进行了受试者工作特征曲线(ROC)分析。此外,分析了CD43和CD200在诊断CLL中的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。共纳入137例患者。CLL组87例患者,非CLL组50例患者。曼-惠特尼U检验显示,与非CLL患者相比,CLL患者中CD43表达(U = 997.5,Z = - 5.265,P < 0.001)和CD200表达(U = 932.0,Z = - 5.5,P < 0.01)有显著差异。在区分CLL与非CLL组时,CD43和CD200的MFI曲线下面积分别为0.771和0.786。CD43和CD200的MFI最佳截断值分别为1323和1775。CD43诊断CLL病例的敏感性、特异性、PPV和NPV分别为97.7%、66%、83.3%和94.2%。CD200诊断CLL病例的敏感性、特异性、PPV和NPV分别为100%、32%、71.9%和100%。CD43和CD200是鉴别CLL与其他成熟B细胞肿瘤的有用标志物,在CLL中发现这两种标志物的MFI表达更高。