Cargando…
Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma
We studied 190 patients with smoldering multiple myeloma (SMM) at our institution between 1973 and 2014. Evolving change in monoclonal protein level (eMP) was defined as ⩾10% increase in serum monoclonal protein (M) and/or immunoglobulin (Ig) (M/Ig) within the first 6 months of diagnosis (only if M-...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030386/ https://www.ncbi.nlm.nih.gov/pubmed/27471870 http://dx.doi.org/10.1038/bcj.2016.65 |
_version_ | 1782454669841268736 |
---|---|
author | Ravi, P Kumar, S Larsen, J T Gonsalves, W Buadi, F Lacy, M Q Go, R Dispenzieri, A Kapoor, P Lust, J A Dingli, D Lin, Y Russell, S J Leung, N Gertz, M A Kyle, R A Bergsagel, P L Rajkumar, S V |
author_facet | Ravi, P Kumar, S Larsen, J T Gonsalves, W Buadi, F Lacy, M Q Go, R Dispenzieri, A Kapoor, P Lust, J A Dingli, D Lin, Y Russell, S J Leung, N Gertz, M A Kyle, R A Bergsagel, P L Rajkumar, S V |
author_sort | Ravi, P |
collection | PubMed |
description | We studied 190 patients with smoldering multiple myeloma (SMM) at our institution between 1973 and 2014. Evolving change in monoclonal protein level (eMP) was defined as ⩾10% increase in serum monoclonal protein (M) and/or immunoglobulin (Ig) (M/Ig) within the first 6 months of diagnosis (only if M-protein ⩾3 g/dl) and/or ⩾25% increase in M/Ig within the first 12 months, with a minimum required increase of 0.5 g/dl in M-protein and/or 500 mg/dl in Ig. Evolving change in hemoglobin (eHb) was defined as ⩾0.5 g/dl decrease within 12 months of diagnosis. A total of 134 patients (70.5%) progressed to MM over a median follow-up of 10.4 years. On multivariable analysis adjusting for factors known to predict for progression to MM, bone marrow plasma cells ⩾20% (odds ratio (OR)=3.37 (1.30–8.77), P=0.013), eMP (OR=8.20 (3.19–21.05), P<0.001) and eHb (OR=5.86 (2.12–16.21), P=0.001) were independent predictors of progression within 2 years of SMM diagnosis. A risk model comprising these variables was constructed, with median time to progression of 12.3, 5.1, 2.0 and 1.0 years among patients with 0–3 risk factors respectively. The 2-year progression risk was 81.5% in individuals who demonstrated both eMP and eHb, and 90.5% in those with all three risk factors. |
format | Online Article Text |
id | pubmed-5030386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50303862016-09-26 Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma Ravi, P Kumar, S Larsen, J T Gonsalves, W Buadi, F Lacy, M Q Go, R Dispenzieri, A Kapoor, P Lust, J A Dingli, D Lin, Y Russell, S J Leung, N Gertz, M A Kyle, R A Bergsagel, P L Rajkumar, S V Blood Cancer J Original Article We studied 190 patients with smoldering multiple myeloma (SMM) at our institution between 1973 and 2014. Evolving change in monoclonal protein level (eMP) was defined as ⩾10% increase in serum monoclonal protein (M) and/or immunoglobulin (Ig) (M/Ig) within the first 6 months of diagnosis (only if M-protein ⩾3 g/dl) and/or ⩾25% increase in M/Ig within the first 12 months, with a minimum required increase of 0.5 g/dl in M-protein and/or 500 mg/dl in Ig. Evolving change in hemoglobin (eHb) was defined as ⩾0.5 g/dl decrease within 12 months of diagnosis. A total of 134 patients (70.5%) progressed to MM over a median follow-up of 10.4 years. On multivariable analysis adjusting for factors known to predict for progression to MM, bone marrow plasma cells ⩾20% (odds ratio (OR)=3.37 (1.30–8.77), P=0.013), eMP (OR=8.20 (3.19–21.05), P<0.001) and eHb (OR=5.86 (2.12–16.21), P=0.001) were independent predictors of progression within 2 years of SMM diagnosis. A risk model comprising these variables was constructed, with median time to progression of 12.3, 5.1, 2.0 and 1.0 years among patients with 0–3 risk factors respectively. The 2-year progression risk was 81.5% in individuals who demonstrated both eMP and eHb, and 90.5% in those with all three risk factors. Nature Publishing Group 2016-07 2016-07-29 /pmc/articles/PMC5030386/ /pubmed/27471870 http://dx.doi.org/10.1038/bcj.2016.65 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Ravi, P Kumar, S Larsen, J T Gonsalves, W Buadi, F Lacy, M Q Go, R Dispenzieri, A Kapoor, P Lust, J A Dingli, D Lin, Y Russell, S J Leung, N Gertz, M A Kyle, R A Bergsagel, P L Rajkumar, S V Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title | Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title_full | Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title_fullStr | Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title_full_unstemmed | Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title_short | Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
title_sort | evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030386/ https://www.ncbi.nlm.nih.gov/pubmed/27471870 http://dx.doi.org/10.1038/bcj.2016.65 |
work_keys_str_mv | AT ravip evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT kumars evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT larsenjt evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT gonsalvesw evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT buadif evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT lacymq evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT gor evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT dispenzieria evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT kapoorp evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT lustja evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT dinglid evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT liny evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT russellsj evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT leungn evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT gertzma evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT kylera evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT bergsagelpl evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma AT rajkumarsv evolvingchangesindiseasebiomarkersandriskofearlyprogressioninsmolderingmultiplemyeloma |