无症状的
多发性骨髓瘤
医学
不确定意义的单克隆抗体病
人口
恶性肿瘤
阶段(地层学)
重症监护医学
内科学
肿瘤科
单克隆
免疫学
单克隆抗体
抗体
古生物学
环境卫生
生物
作者
Sæmundur Rögnvaldsson,Sigrún Þorsteinsdóttir,Sigurður Y. Kristinsson
出处
期刊:Clinical Chemistry
[Oxford University Press]
日期:2024-01-01
卷期号:70 (1): 128-139
被引量:2
标识
DOI:10.1093/clinchem/hvad148
摘要
Abstract Background Multiple myeloma (MM) is a hematological malignancy that develops over years from the asymptomatic precursors, monoclonal gammopathy of undetermined significance, and smoldering multiple myeloma. Recent evidence shows that by initiating treatment at an asymptomatic stage, outcomes in MM can be significantly improved. However, a vast majority of MM patients are diagnosed after the development of symptomatic end-organ damage and cannot reap the benefits of early treatment. The precursors of MM are easily detected by serum protein electrophoresis and free light chain assay of the serum, raising the question of whether population-based screening could detect MM at an asymptomatic stage and significantly expand the availability of early treatment in MM. Screening is a hallmark of care in many malignancies, and there are accepted criteria for when screening is appropriate. Content Here we review the available relevant evidence for the introduction of screening and discuss whether screening for MM and its precursors fulfills these criteria. We also highlight gaps in our current knowledge, most notably a lack of data on the benefits and harms of screening and the lack of a defined target population. There are ongoing studies that may fill these critical gaps in the literature, but their results are still pending. Summary Screening could lead to a paradigm shift in the care of patients with MM, but critical scientific questions need to be answered before screening of healthy individuals can be recommended. In short, we should not screen for MM and its precursors—yet.
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