Comparison of flowcytometry-based scoring system for the diagnosis of early T precursor-acute lymphoblastic leukemia

IF 2.3 3区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY Cytometry Part B: Clinical Cytometry Pub Date : 2023-03-09 DOI:10.1002/cyto.b.22119
Deepak Marballi Basavaraju, Shruti Mishra, Gaurav Chhabra, Sudarshan Chougule
{"title":"Comparison of flowcytometry-based scoring system for the diagnosis of early T precursor-acute lymphoblastic leukemia","authors":"Deepak Marballi Basavaraju,&nbsp;Shruti Mishra,&nbsp;Gaurav Chhabra,&nbsp;Sudarshan Chougule","doi":"10.1002/cyto.b.22119","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Early T cell precursor-acute lymphoblastic leukemia (ETP-ALL) is a hematolymphoid malignancy where the blasts demonstrate T cell differentiation markers along with stem cell and myeloid antigen expression. The differential diagnosis of ETP-ALL from non-ETP ALL and mixed phenotype acute leukemia is often challenging due to its overlapping immunophenotypic picture with co-expression of myeloid antigens. In this study, we endeavored to describe the immune-phenotype profile of ETP-ALL in our patients and compared the utility of four different scoring systems for better discrimination of these entities.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>This retrospective analysis included 31 ETP-ALL out of 860 acute leukemia cases consecutively diagnosed at the two tertiary care centers. Flowcytometry-based immunophenotype was reviewed for all the cases, and the utility of four flow-based objective scorings was assessed for the diagnosis of ETP-ALL. Receiver operating curves were drawn to compare the different flow-based scoring systems.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The prevalence of ETP-ALL was 40% (<i>n</i> = 31/77 T-ALL) in our study group, comprised mainly of adults with a median age of 20 years. The five-marker scoring system had the maximum area under the curve, followed by the seven-marker scoring system. A cut-off of ≥2.5 was more specific (sensitivity: 91%; specificity: 100%), while a score of ≥1.5 was more sensitive but slightly less specific (sensitivity: 94%, specificity: 96%).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>The WHO criteria for the diagnosis of ETP-ALL should be followed across all laboratories to avoid confusion and for better treatment stratification. Flow-based scoring systems can be objectively employed for better detection of cases.</p>\n </section>\n </div>","PeriodicalId":10883,"journal":{"name":"Cytometry Part B: Clinical Cytometry","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2023-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytometry Part B: Clinical Cytometry","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cyto.b.22119","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Early T cell precursor-acute lymphoblastic leukemia (ETP-ALL) is a hematolymphoid malignancy where the blasts demonstrate T cell differentiation markers along with stem cell and myeloid antigen expression. The differential diagnosis of ETP-ALL from non-ETP ALL and mixed phenotype acute leukemia is often challenging due to its overlapping immunophenotypic picture with co-expression of myeloid antigens. In this study, we endeavored to describe the immune-phenotype profile of ETP-ALL in our patients and compared the utility of four different scoring systems for better discrimination of these entities.

Methods

This retrospective analysis included 31 ETP-ALL out of 860 acute leukemia cases consecutively diagnosed at the two tertiary care centers. Flowcytometry-based immunophenotype was reviewed for all the cases, and the utility of four flow-based objective scorings was assessed for the diagnosis of ETP-ALL. Receiver operating curves were drawn to compare the different flow-based scoring systems.

Results

The prevalence of ETP-ALL was 40% (n = 31/77 T-ALL) in our study group, comprised mainly of adults with a median age of 20 years. The five-marker scoring system had the maximum area under the curve, followed by the seven-marker scoring system. A cut-off of ≥2.5 was more specific (sensitivity: 91%; specificity: 100%), while a score of ≥1.5 was more sensitive but slightly less specific (sensitivity: 94%, specificity: 96%).

Conclusion

The WHO criteria for the diagnosis of ETP-ALL should be followed across all laboratories to avoid confusion and for better treatment stratification. Flow-based scoring systems can be objectively employed for better detection of cases.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于流式细胞术的评分系统在诊断早期T前体-急性淋巴细胞白血病方面的比较
背景 早期 T 细胞前体-急性淋巴细胞白血病(ETP-ALL)是一种血淋巴细胞恶性肿瘤,其胚胎表现出 T 细胞分化标记以及干细胞和髓系抗原表达。ETP-ALL与非ETP ALL和混合表型急性白血病的鉴别诊断往往具有挑战性,因为其免疫表型与髓抗原的共同表达存在重叠。在本研究中,我们试图描述 ETP-ALL 患者的免疫表型特征,并比较四种不同评分系统的效用,以更好地区分这些实体。 方法 这项回顾性分析包括两个三级医疗中心连续诊断的 860 例急性白血病病例中的 31 例 ETP-ALL。对所有病例进行了基于流式细胞术的免疫表型审查,并评估了四种基于流式细胞术的客观评分对诊断 ETP-ALL 的实用性。绘制了接收者操作曲线,以比较不同的流式评分系统。 结果 在我们的研究小组中,ETP-ALL的发病率为40%(n = 31/77 T-ALL),主要由中位年龄为20岁的成年人组成。五指标评分系统的曲线下面积最大,其次是七指标评分系统。≥2.5分界点的特异性更高(灵敏度:91%;特异性:100%),而≥1.5分界点的灵敏度更高,但特异性稍低(灵敏度:94%;特异性:96%)。 结论 所有实验室都应遵循世界卫生组织的 ETP-ALL 诊断标准,以避免混淆并更好地进行治疗分层。基于流程的评分系统可客观地用于更好地检测病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.80
自引率
32.40%
发文量
51
审稿时长
>12 weeks
期刊介绍: Cytometry Part B: Clinical Cytometry features original research reports, in-depth reviews and special issues that directly relate to and palpably impact clinical flow, mass and image-based cytometry. These may include clinical and translational investigations important in the diagnostic, prognostic and therapeutic management of patients. Thus, we welcome research papers from various disciplines related [but not limited to] hematopathologists, hematologists, immunologists and cell biologists with clinically relevant and innovative studies investigating individual-cell analytics and/or separations. In addition to the types of papers indicated above, we also welcome Letters to the Editor, describing case reports or important medical or technical topics relevant to our readership without the length and depth of a full original report.
期刊最新文献
CD38, CD39, and BCL2 differentiate disseminated forms of high-grade B-cell lymphomas in biological fluids from Burkitt lymphoma and diffuse large B-cell lymphoma. Converting an HLA‐B27 flow assay from the BD FACSCanto to the BD FACSLyric A comprehensive 26‐color immunophenotyping panel to study the role of the gut‐liver axis in chronic liver diseases CD133 in T-lymphoblastic leukemia is preferentially expressed in early T-phenotype (ETP) and near ETP subtypes. Appropriate interpretation of TRBC1-dim positive subsets in T-cell immunophenotyping by flow cytometry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1