Abstract
Follow-up of low-risk monoclonal gammopathy of undetermined significance (MGUS) is debated as multiple myeloma (MM) progression risk is low. Worse MM outcome was reported for patients followed for low-risk MGUS, possibly due to less optimal follow-up. However, it is unknown whether progressing low-risk MGUS is associated with aggressive tumor behavior. Understanding these patterns is crucial for MGUS management. Here, we investigated whether progression from low-risk MGUS is associated with worse MM outcome in patients who had no MGUS follow-up before myeloma diagnosis. We retrospectively determined the MGUS status in repeated pre-diagnostic blood samples prospectively collected from 42 myeloma patients in median 11.6 years (first sample) and 3.3 years (repeated sample) before myeloma diagnosis. At first pre-diagnostic blood draw, 12 had low-risk (defined by an immunoglobulin [Ig] G monoclonal [M] spike < 15 g/L and a normal free light-chain ratio) and 30 had MGUS of other risk. MM bone disease was more common in patients with low-risk MGUS at first blood draw (67% vs. 30%, P = 0.041). Median survival since myeloma diagnosis was worse in low-risk than other MGUS at first blood draw (2.3 vs. 7.5 years, P = 0.004). Modest progression was observed between first and repeated blood draw for the majority of low-risk MGUS as 67% remained as low- or low-intermediate-risk MGUS at repeated blood draw. Our study, albeit limited by its small size, indicates that progression from low-risk MGUS is associated with worse MM outcome regardless of MGUS follow-up. Although further investigation is needed, progressing low-risk MGUS could belong to a group of aggressive tumors with progression that is difficult to predict.
Highlights
Follow-up of low-risk monoclonal gammopathy of undetermined significance (MGUS) is debated as multiple mye‐ loma (MM) progression risk is low
Guidelines recommend following MGUS according to MM progression risk [3]
We investigated whether progression from low-risk MGUS
Summary
Follow-up of low-risk monoclonal gammopathy of undetermined significance (MGUS) is debated as multiple mye‐ loma (MM) progression risk is low. We could study natural progression patterns in relation to MM outcome because 42 had detectable MGUS (protein and immunofixation electrophoresis and free light-chain assays) in both pre-diagnostic samples without MGUS follow-up before myeloma diagnosis. The first pre-diagnostic blood sample was donated in November 1986 and the last follow-up since myeloma diagnosis was in February 2021 providing a 19-year study duration in median.
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