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首页> 外文期刊>Cytometry, Part B. Clinical cytometry: the journal of the International Society for Analytical Cytology >External quality assurance of circulating tumor cell enumeration using the CellSearch? system: A feasibility study
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External quality assurance of circulating tumor cell enumeration using the CellSearch? system: A feasibility study

机译:使用CellSearch进行循环肿瘤细胞计数的外部质量保证?系统:可行性研究

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Background: Circulating tumor cells (CTCs) are cells that have detached from solid tumors and entered the blood. CTCs can be detected, among others, by semi-automated immunomagnetic enrichment and image cytometry using CellSearch? (Veridex, Raritan, NJ). We studied the feasibility of external quality assurance (EQA) of the entire CellSearch procedure from blood draw to interpretation of results in multiple laboratories. Methods: Blood samples from six cancer patients and controls were distributed to 14 independent laboratories to test between-laboratory, between-assay, and between-instrument variation. Additionally, between-operator variability was assessed through the interpretation of blinded images of all blood samples on a website. Results: Shipment and storage of samples had no influence on CTC values. Between-instrument (coefficient of variation (CV) < 12%) and between-assay variation was low (CV ≤ 20%), indicating high reproducibility. However, between-laboratory CV ranged from 45 to 64%. Although inter-operator agreement on image interpretation (Fleiss' I° statistics) ranged from " to "almost perfect," image interpretation, particularly of samples containing high numbers of apoptotic cells, was the main contributor to between-laboratory variation. Conclusions: This multicenter study shows the feasibility of an EQA program for CTC detection in patient samples, and the importance of continuation of such a program for the harmonization of CTC enumeration.
机译:背景:循环肿瘤细胞(CTC)是已从实体肿瘤脱离并进入血液的细胞。可以通过半自动免疫磁富集和使用CellSearch?的图像细胞术检测CTC。 (Veridex,Raritan,NJ)。我们研究了从血液抽取到多个实验室结果解释的整个CellSearch程序的外部质量保证(EQA)的可行性。方法:将六名癌症患者和对照组的血液样本分配到14个独立的实验室,以测试实验室之间,测定之间和仪器之间的差异。此外,通过解释网站上所有血液样本的盲图来评估操作员之间的差异。结果:样品的运输和储存对CTC值没有影响。仪器之间(变异系数(CV)<12%)和测定间变异低(CV≤20%),表明可重复性高。但是,实验室之间的简历范围从45%到64%。尽管操作员之间关于图像解释的协议(Fleiss的I°统计)的范围从“到”几乎“完美”,但是图像解释(尤其是包含大量凋亡细胞的样品)的图像解释是实验室间变异的主要原因。多中心研究表明,在患者样品中进行CTC检测的EQA计划的可行性,以及继续实施此类程序以协调CTC枚举的重要性。

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