分析急性早幼粒细胞白血病(APML)的“泪滴”印迹:流式细胞术预测APML的免疫表型。

American journal of blood research Pub Date : 2021-08-15 eCollection Date: 2021-01-01
Fouzia Siraj, Pranay Tanwar, Amitabh Singh, Bhavika Rishi, Amar Ranjan, Anita Chopra, Sandeep Rai, Sameer Bakhshi, Aroonima Misra
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引用次数: 0

摘要

急性早幼粒细胞白血病(Acute promyelocytic leukemia, APML)虽然在遗传和形态学上不同于其他AML(急性髓性白血病)亚型,但却是最具反应性的急性髓性白血病之一。常规诊断方法和形态学提示在大多数情况下,由于资源限制,无法获得细胞遗传学检查,次颗粒变异,aml单核细胞和骨髓单核细胞的形态模仿等,在外围实验室往往失败。然而,流式细胞术(FCM)可以作为一种可行且可靠的免疫表型诊断和预后工具,用于快速识别APML。为了快速和敏感地诊断APML,我们打算建议一种成本有效的、敏感的FCM面板,并对患者进行预后。材料与方法:本研究回顾性分析了123例急性早幼粒细胞白血病的流式细胞术特征,其中包括40例下颗粒变异。标记物表达量与平均荧光强度(MFI)和标记物表达率进行比较。与急性单核细胞白血病病例进行了非统计学比较。根据患者的免疫表型特征和表达进行分组,并采用多因素logistic回归进行MFI比较。将诊断和缓解流量试验阳性的异常标志物与生存结果进行比较,并计算其阳性预测值。结果:除低侧散度的亚颗粒型外,窗侧散度最大的特征是无爆炸,侧散度高。免疫表型特征为CD117, cMPO阳性,明亮的CD33和CD13阳性,缺乏CD34和HLA-DR在大多数APML中可见,包括亚颗粒型变异。我们建议快速诊断四管面板快速和快速诊断APML,包括100%敏感性的下颗粒变异。该研究还确定了六组具有重要APML预测价值的免疫表型,包括下颗粒变异。该研究还强调了CD2、CD56和CD9作为急性早幼粒细胞白血病的预后标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Analysing "tear-drop" prints of acute promyelocytic leukemia (APML): immunophenotypic prognostication of APML by FCM.

Analysing "tear-drop" prints of acute promyelocytic leukemia (APML): immunophenotypic prognostication of APML by FCM.

Introduction: Acute promyelocytic leukemia (APML), although genetically and morphologically distinct from other AML (acute myeloid leukemia) subtypes, is one of the most best responsive acute myeloid leukemia. -Conventional diagnostic methods and morphological hints often fail in the majority of the cases in the peripheral laboratories owing to resource constraints, unavailability of cytogenetic work-up, hypogranular variants, morphological mimicry by AML-monocytic and myelo-monocytic, etc. Flowcytometry (FCM), however, can be utilized as a feasible and reliable immunophenotypic diagnostic and prognostic tool for prompt identification of APML. In order to rapidly and sensitively diagnose APML we intended to suggest a cost effective, sensitive FCM panel and also to prognositicate patients.

Material and methods: In this retrospective study, flowcytometry characteristics of 123 cases of acute promyelocytic leukemia were studied including 40 hypogranular variants. The expression of markers was compared with the Mean flurescent Intensity (MFI) and percent expression of markers. A non-statistical comparison was made with cases of acute monocytic leukemia. The cases were grouped according to their immunophenotype characteristics and expression with comparison of MFI by multivariate logistic regression. The aberrant markers positive at diagnostic and remission flow test were compared with the survival outcomes, and their positive predictive values were calculated.

Results: The most common feature of side scatter property was the absence of blasts in the window and high side scatter, except hypogranular variants which had low side scatter. Immunophenotypically characterised by positivity for CD117, cMPO, and bright CD33 and CD13 positivity and lack of CD34 and HLA-DR was seen in the majority of APML including hypo-granular variant. We suggest a rapid diagnostic four-tube panel for fast and rapid diagnosis of APML, including hypogranular variants with 100% sensitivity. The study also identified six groups of immunophenotypes with significant prediction values of APML, including hypogranular variants. The study also highlights CD2, CD56, and CD9 as prognostic markers for acute promyelocytic leukemia.

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American journal of blood research
American journal of blood research MEDICINE, RESEARCH & EXPERIMENTAL-
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