| Literature DB >> 29506935 |
Charlotte Cosemans1, Bénedith Oben2, Ingrid Arijs1, Annick Daniëls3, Jeroen Declercq3, Kimberly Vanhees4, Guy Froyen5, Brigitte Maes5, Jeroen Mebis6, Jean-Luc Rummens7.
Abstract
Multiple myeloma (MM), characterized by malignant plasma cells in the bone marrow, is consistently preceded by asymptomatic premalignant stage monoclonal gammopathy of undetermined significance (MGUS). These MGUS patients have an annual risk of 1% to progress to MM. Clinical, imaging, and genomic (genetic and epigenetic) factors were identified, whose presence increased the risk of progression from MGUS to MM. In this systematic review we summarize the currently identified clinical, imaging, and genomic biomarkers suggested to increase the progression risk or shown to be differentially expressed/present between both cohorts of patients. Despite the wide range of proposed markers, there are still no reliable biomarkers to individually predict which MGUS patient will progress to MM and which will not. Research on biomarkers in the progression from MGUS to MM will give more insight in the unknown pathogenesis of this hematological malignancy. This would improve research by elucidating new pathways and potential therapeutic targets as well as clinical management by closer follow-up and earlier treatment of high-risk MGUS patients.Entities:
Keywords: Biological marker; Disease progression; Hematological malignancy; Premalignant stage; Risk factors
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Year: 2018 PMID: 29506935 DOI: 10.1016/j.clml.2018.02.011
Source DB: PubMed Journal: Clin Lymphoma Myeloma Leuk ISSN: 2152-2669