基于 p210 和 p190 BCR::ABL1 参考材料的 BCR::ABL1 标准化系统新实践。

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Yu Ma , Yanxi Han , Zhenli Diao , Yuqing Chen , Tao Huang , Lei Feng , Jian Jiang , Yuanfeng Zhang , Jinming Li , Rui Zhang
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引用次数: 0

摘要

BCR::ABL1 定量可监测最小残留病,因此对患者分层至关重要。虽然在提高p210 BCR::ABL1定量的准确性方面取得了重大进展,但p190 BCR::ABL1尚未进行同等的标准化。因此,我们开发了 p190 BCR::ABL1 参考材料,通过基于质粒的创新校准策略来校准定量过程。随后,我们进一步探讨了在全国 159 个实验室使用 p190 和 p210 参考材料进行标准化检测的情况,并利用质量评估样本评估了它们的检测能力。结果表明,经过校准后,p190 的检测结果变异系数从 50.8 %-57.4 % 降至 24.9 %-36.4 %,p210 的检测结果变异系数从 37.6 %-49.0 % 降至 19.1 %-28.5 %。在 2023S21-2023S24 中,p190 样品的目标值在± 2 倍以内的实验室比例从 77.1%、76.4%、73.2% 和 74.5% 提高到 94.3%、95.5%、92.4% 和 91.1%;在 2023S11-2023S14 中,p210 样品的目标值在± 2 倍以内的实验室比例从 72.3%、86.2%、79.2% 和 81.1% 提高到 98.1%、99.4%、98.1% 和 96.2%。总之,我们的研究成功地开发并使用了 p190 和 p210 参考材料,提高了实验室间 BCR::ABL1 定量的准确性和可比性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New practice of BCR::ABL1 standardization system based on p210 and p190 BCR::ABL1 reference materials
Quantification of BCR::ABL1 monitors minimal residual disease, thus critical for patient stratification. While significant progress has been made in enhancing the accuracy of p210 BCR::ABL1 quantification, no equivalent standardization has been conducted for p190 BCR::ABL1. Therefore, we developed p190 BCR::ABL1 reference materials to calibrate the quantitative process through an innovative plasmid-based calibration strategy. Then, we further explored the use of p190 and p210 reference materials to standardize tests in 159 laboratories across China and assessed their detection capability utilizing quality assessment samples. Results suggested that after calibration, the coefficient of variation of detection results decreased from 50.8 %–57.4 % to 24.9 %–36.4 % for p190, and from 37.6 %–49.0 % to 19.1 %–28.5 % for p210. The percentage of laboratories within ± 2-fold of the target values increased from 77.1 %, 76.4 %, 73.2 %, and 74.5 % to 94.3 %, 95.5 %, 92.4 %, and 91.1 % for p190 samples 2023S21–2023S24, and from 72.3 %, 86.2 %, 79.2 %, and 81.1 % to 98.1 %, 99.4 %, 98.1 %, and 96.2 % for p210 samples 2023S11–2023S14. Overall, our study successfully developed and employed p190 and p210 reference materials to promote accuracy and comparability of BCR::ABL1 quantification among laboratories.
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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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