Related Experiment Video
Updated: Feb 13, 2026

An Organotypic High Throughput System for Characterization of Drug Sensitivity of Primary Multiple Myeloma Cells
Published on: July 15, 2015
Prognostic Biomarkers in the Progression From MGUS to Multiple Myeloma: A Systematic Review
Charlotte Cosemans1, Bénedith Oben1, Ingrid Arijs1
1Department of Experimental Hematology, Jessa Hospital, Hasselt, Belgium; Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium.
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.
Insights
Monoclonal gammopathy of undetermined significance (MGUS) can progress to multiple myeloma (MM). While clinical, imaging, and genomic factors are known, reliable biomarkers for individual risk prediction are still lacking.
Area of Science:
- Hematology
- Oncology
- Biomarker Research
Background:
- Multiple myeloma (MM) originates from a premalignant stage, monoclonal gammopathy of undetermined significance (MGUS).
- MGUS patients face an annual 1% risk of progressing to MM.
- Identifying progression risk factors is crucial for early intervention.
Purpose of the Study:
- To systematically review identified clinical, imaging, and genomic biomarkers associated with MGUS progression to MM.
- To summarize differentially expressed markers between MGUS and MM patient cohorts.
- To highlight the need for reliable predictive biomarkers.
Main Methods:
- Systematic literature review.
- Identification and summarization of clinical, imaging, and genomic factors.
- Analysis of biomarkers differentiating MGUS and MM.
Main Results:
- Various clinical, imaging, and genomic factors have been linked to increased progression risk.
- Despite identified factors, no single reliable biomarker can predict individual progression from MGUS to MM.
- A significant gap exists in precise individual risk stratification.
Conclusions:
- Current biomarkers are insufficient for predicting individual MGUS to MM progression.
- Further research into biomarkers is essential for understanding MM pathogenesis.
- Developing reliable biomarkers could enable closer monitoring and earlier treatment of high-risk patients.
Related Concept Videos
Review and Preview
Percentiles are a type of fractile that partition data into...
Review and Preview
Random and Systematic Errors
Systematic Sampling Method
Systematic sampling is one of the simplest methods...
Propagation of Uncertainty from Systematic Error
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...

