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Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients
PURPOSE: Monoclonal gammopathy of undetermined significance (MGUS) is a premalignancy preceding multiple myeloma (MM) or related disorders. In MGUS, renal impairment caused by deposition of the monoclonal immunoglobulins or free light-chains monoclonal gammopathy of renal significance (MGRS) is ofte...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788644/ https://www.ncbi.nlm.nih.gov/pubmed/29416776 http://dx.doi.org/10.18632/oncotarget.23412 |
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author | Steiner, Normann Göbel, Georg Suchecki, Patricia Prokop, Wolfgang Neuwirt, Hannes Gunsilius, Eberhard |
author_facet | Steiner, Normann Göbel, Georg Suchecki, Patricia Prokop, Wolfgang Neuwirt, Hannes Gunsilius, Eberhard |
author_sort | Steiner, Normann |
collection | PubMed |
description | PURPOSE: Monoclonal gammopathy of undetermined significance (MGUS) is a premalignancy preceding multiple myeloma (MM) or related disorders. In MGUS, renal impairment caused by deposition of the monoclonal immunoglobulins or free light-chains monoclonal gammopathy of renal significance (MGRS) is often associated with high morbidity and mortality. We analysed the prevalence of renal impairment, clinical features and the long-term outcome in 2935 patients with MGUS. METHODS: Between 1/2000 and 8/2016, 2935 adult patients with MGUS were identified in our database. RESULTS: In 44/2935 (1.5%) patients MGRS was diagnosed. In MGRS patients, significantly more progressions to MM were observed than in MGUS patients (18% vs. 3%; P<0.001). MGRS patients showed a higher risk for progression (HR 3.3 [1.5-7.4]) in the Cox model. Median time to progression was 23 years for MGUS and 18.8 years for MGRS patients. Corresponding progression rate was 8.8 [7.2-10.7] per 1000 patient-years (py) for MGUS patients and 30.6 [15.3–61] for the MGRS group. Risk for progression within the first year after diagnosis was 1% [0.6-1.4] in the MGUS group and 10% [4-29] among MGRS patients. CONCLUSION: The significantly higher risk for progression to MM means MGRS patients should be monitored carefully and treated in a specialized centre. |
format | Online Article Text |
id | pubmed-5788644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57886442018-02-07 Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients Steiner, Normann Göbel, Georg Suchecki, Patricia Prokop, Wolfgang Neuwirt, Hannes Gunsilius, Eberhard Oncotarget Research Paper PURPOSE: Monoclonal gammopathy of undetermined significance (MGUS) is a premalignancy preceding multiple myeloma (MM) or related disorders. In MGUS, renal impairment caused by deposition of the monoclonal immunoglobulins or free light-chains monoclonal gammopathy of renal significance (MGRS) is often associated with high morbidity and mortality. We analysed the prevalence of renal impairment, clinical features and the long-term outcome in 2935 patients with MGUS. METHODS: Between 1/2000 and 8/2016, 2935 adult patients with MGUS were identified in our database. RESULTS: In 44/2935 (1.5%) patients MGRS was diagnosed. In MGRS patients, significantly more progressions to MM were observed than in MGUS patients (18% vs. 3%; P<0.001). MGRS patients showed a higher risk for progression (HR 3.3 [1.5-7.4]) in the Cox model. Median time to progression was 23 years for MGUS and 18.8 years for MGRS patients. Corresponding progression rate was 8.8 [7.2-10.7] per 1000 patient-years (py) for MGUS patients and 30.6 [15.3–61] for the MGRS group. Risk for progression within the first year after diagnosis was 1% [0.6-1.4] in the MGUS group and 10% [4-29] among MGRS patients. CONCLUSION: The significantly higher risk for progression to MM means MGRS patients should be monitored carefully and treated in a specialized centre. Impact Journals LLC 2017-12-18 /pmc/articles/PMC5788644/ /pubmed/29416776 http://dx.doi.org/10.18632/oncotarget.23412 Text en Copyright: © 2018 Steiner et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Steiner, Normann Göbel, Georg Suchecki, Patricia Prokop, Wolfgang Neuwirt, Hannes Gunsilius, Eberhard Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title | Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title_full | Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title_fullStr | Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title_full_unstemmed | Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title_short | Monoclonal gammopathy of renal significance (MGRS) increases the risk for progression to multiple myeloma: an observational study of 2935 MGUS patients |
title_sort | monoclonal gammopathy of renal significance (mgrs) increases the risk for progression to multiple myeloma: an observational study of 2935 mgus patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788644/ https://www.ncbi.nlm.nih.gov/pubmed/29416776 http://dx.doi.org/10.18632/oncotarget.23412 |
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