Limvorapitak Wasithep, Srisum-Ang Thammasiree, Chimres Chutima, Warnnissorn Naree, Kanitsap Nonglak
Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Thammasat University, Pathumthani, Thailand.
Pathology Unit, Thammasat University Hospital, Pathumthani, Thailand.
Clin Lymphoma Myeloma Leuk. 2016 Mar;16(3):e27-37. doi: 10.1016/j.clml.2015.12.002. Epub 2015 Dec 17.
Plasma cell neoplasm is a common hematologic malignancy. Treatment with novel agents results in favorable outcomes. Reliable investigations are required to monitor the residual disease, especially after such effective treatments. Flow cytometric analysis is a speedy and accurate method to detect abnormal cells. The aim of this study was to determine diagnostic performance of flow cytometry in the detection of abnormal plasma cells in bone marrow specimens.
We included bone marrow samples taken from patients suspected to harbor plasma cell neoplasm at the time of diagnosis or follow-up after treatment from 2013 to 2015. Flow cytometric analyses, using cluster of differentiation (CD)19/CD20/CD27/CD38/CD45/CD56/CD117/CD138 and cytoplasmic κ/λ, were done and results compared with morphologic evaluation of marrow aspirate smear, histology, and immunohistochemistry of marrow biopsy and protein electrophoretic analyses.
A total of 154 specimens were included. Plasma cell neoplasm was detected in 56 samples (36.4%). Most abnormal plasma cells in this study were CD19-negative (CD19(-))/CD20(-)/CD27(+)/CD38(+)/CD45(-) (or weakly positive)/CD56(+)/CD117(+)/CD138(+). Light chain restriction was found only in 18 samples (32.1%). Sensitivity and specificity of flow cytometric analysis were 91.1% and 96.9%, respectively. For the follow-up cohort, sensitivity and specificity were 86.7% and 66.7%, respectively.
Analysis of plasma cell neoplasm using flow cytometry has high sensitivity and specificity. As an adjunct to marrow histology and immunohistochemistry, flow cytometry can be used in diagnosis of plasma cell neoplasm and more importantly in monitoring the disease after treatment. We propose a limited panel of CD19/CD38/CD45/CD56/CD117/CD138 for detecting minimal residual disease in Thai patients.
浆细胞肿瘤是一种常见的血液系统恶性肿瘤。使用新型药物治疗可带来良好的治疗效果。需要可靠的检查来监测残留疾病,尤其是在进行此类有效治疗之后。流式细胞术分析是一种快速、准确检测异常细胞的方法。本研究的目的是确定流式细胞术在检测骨髓标本中异常浆细胞的诊断性能。
我们纳入了2013年至2015年期间在诊断时或治疗后随访期间疑似患有浆细胞肿瘤的患者的骨髓样本。使用分化簇(CD)19/CD20/CD27/CD38/CD45/CD56/CD117/CD138和细胞质κ/λ进行流式细胞术分析,并将结果与骨髓穿刺涂片的形态学评估、组织学、骨髓活检的免疫组织化学以及蛋白质电泳分析进行比较。
共纳入154份标本。在56份样本(36.4%)中检测到浆细胞肿瘤。本研究中大多数异常浆细胞为CD19阴性(CD19(-))/CD20(-)/CD27(+)/CD38(+)/CD45(-)(或弱阳性)/CD56(+)/CD117(+)/CD138(+)。仅在18份样本(32.1%)中发现轻链限制。流式细胞术分析的敏感性和特异性分别为91.1%和96.9%。对于随访队列,敏感性和特异性分别为86.7%和66.7%。
使用流式细胞术分析浆细胞肿瘤具有高敏感性和特异性。作为骨髓组织学和免疫组织化学的辅助手段,流式细胞术可用于浆细胞肿瘤的诊断,更重要的是用于治疗后疾病的监测。我们建议使用有限的CD19/CD38/CD45/CD56/CD117/CD138组合来检测泰国患者的微小残留疾病。