# Monoclonal gammopathy of renal significance (MGRS): retrospective monocentric analysis of clinical outcomes and treatment strategies

**Authors:** Pasquale Esposito, Lucia Macciò, Antonia Cagnetta, Francesca Costigliolo, Emilio Venturelli, Elisa Russo, Marco Gallo, Debora Soncini, Francesca Viazzi, Roberto Massimo Lemoli, Michele Cea

PMC · DOI: 10.1007/s10238-025-01646-7 · Clinical and Experimental Medicine · 2025-04-15

## TL;DR

This study examines clinical outcomes and treatment strategies for a rare kidney disorder caused by monoclonal proteins, highlighting differences between two subgroups.

## Contribution

The paper provides a retrospective analysis of MGRS subgroups, revealing distinct clinical features and outcomes.

## Key findings

- MGRS-A had a more aggressive course with shorter survival compared to MGRS-NA.
- Anemia was the most common treatment-related side effect, linked to treatment intensity.
- Baseline factors like hemoglobin and CRP levels predicted mortality in MGRS patients.

## Abstract

Monoclonal Gammopathy of Renal Significance (MGRS) is a group of rare disorders in which monoclonal proteins cause kidney damage. Due to its rarity, ongoing research is vital to refine diagnostics, enhance treatment, and improve outcomes. This retrospective study analyzed 34 patients with renal biopsy-proven MGRS-defining lesions. Patients were divided into two subgroups: kidney-limited AL amyloidosis (MGRS-A, 44%, n = 15) and other MGRS (MGRS-NA, 56%, n = 19). Key outcomes included progression-free survival and overall survival. Baseline characteristics such as histopathology, plasma cell percentage, kidney function, and proteinuria were documented alongside initial treatments, and hematologic and renal response. Distinct differences were observed between the two groups: MGRS-NA was primarily associated with glomerular lesions, while MGRS-A exhibited broader kidney involvement. Treatment varied: bortezomib for plasma cell-driven cases and rituximab for B-cell-related conditions. Anemia was the most common side effect (71%), associated with treatment intensity. Despite similar overall survival outcomes, MGRS-A followed a more aggressive course, with a shorter time from diagnosis to death (206 vs. 728 days). Renal and hematologic responses were comparable between the groups, although baseline factors such as hemoglobin and CRP levels were predictive of mortality. These findings underscore the need for more precise characterization and standardized criteria to optimize the management of MGRS.

The online version contains supplementary material available at 10.1007/s10238-025-01646-7.

## Linked entities

- **Chemicals:** bortezomib (PubChem CID 387447)
- **Diseases:** AL amyloidosis (MONDO:0019438), anemia (MONDO:0002280)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Anemia (MESH:D000740), kidney-limited AL amyloidosis (MESH:D000075363), glomerular lesions (MESH:D007674), involvement (MESH:C564676), death (MESH:D003643), MGRS (MESH:D008998), proteinuria (MESH:D011507)
- **Chemicals:** rituximab (MESH:D000069283), bortezomib (MESH:D000069286)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12000252/full.md

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Source: https://tomesphere.com/paper/PMC12000252