质谱法会取代目前多发性骨髓瘤常规监测和MRD检测的技术吗?

IF 0.9 Q4 HEMATOLOGY
Hemato Pub Date : 2021-12-09 DOI:10.3390/hemato2040052
K. Thoren
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引用次数: 2

摘要

近年来,质谱法越来越多地用于检测血清中的单克隆蛋白。质谱分析比血清蛋白电泳和免疫固定更灵敏,可以帮助区分治疗性单克隆抗体和M-蛋白,并可以检测翻译后修饰的存在。质谱法也显示出作为一种微创、基于外周血的检测多发性骨髓瘤最小残留疾病的前景。已经进行了将质谱法的临床实用性与当前基于血液和骨髓的技术进行比较的研究。尽管仍主要局限于研究环境,但临床实验室已开始将这项技术用于患者护理。这篇综述将讨论多发性骨髓瘤质谱检测的现状、这项技术的优势和挑战,以及未来如何将其纳入临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Will Mass Spectrometry Replace Current Techniques for Both Routine Monitoring and MRD Detection in Multiple Myeloma?
In recent years, mass spectrometry has been increasingly used for the detection of monoclonal proteins in serum. Mass spectrometry is more analytically sensitive than serum protein electrophoresis and immunofixation, can help distinguish therapeutic monoclonal antibodies from M-proteins, and can detect the presence of post-translational modifications. Mass spectrometry also shows promise as a less-invasive, peripheral-blood-based test for detecting minimal residual disease in multiple myeloma. Studies comparing the clinical utility of mass spectrometry to current blood- and bone-marrow-based techniques have been conducted. Although still primarily limited to research settings, clinical laboratories are starting to adopt this technique for patient care. This review will discuss the current status of mass spectrometry testing for multiple myeloma, the benefits and challenges of this technique, and how it may be incorporated into clinical practice in the future.
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来源期刊
CiteScore
1.30
自引率
0.00%
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审稿时长
11 weeks
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