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Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma

Little is known about the impact of multiple myeloma (MM) treatment on uninvolved immunoglobulins (Ig). We identified 448 patients who received high-dose dexamethasone (HD-DEX), lenalidomide and dexamethasone (RD), bortezomib and dexamethasone (VD), bortezomib, cyclophosphamide and dexamethasone (VC...

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Autores principales: Ravi, P, Kumar, S, Gonsalves, W, Buadi, F, Lacy, M Q, Go, R S, 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584483/
https://www.ncbi.nlm.nih.gov/pubmed/28622306
http://dx.doi.org/10.1038/bcj.2017.46
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author Ravi, P
Kumar, S
Gonsalves, W
Buadi, F
Lacy, M Q
Go, R S
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
Gonsalves, W
Buadi, F
Lacy, M Q
Go, R S
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 Little is known about the impact of multiple myeloma (MM) treatment on uninvolved immunoglobulins (Ig). We identified 448 patients who received high-dose dexamethasone (HD-DEX), lenalidomide and dexamethasone (RD), bortezomib and dexamethasone (VD), bortezomib, cyclophosphamide and dexamethasone (VCD) or bortezomib, lenalidomide and dexamethasone (VRD) for newly diagnosed MM at our institution between 2000 and 2013, and who had available data on absolute lymphocyte count (ALC) and quantitative uninvolved Ig at baseline and at the end of four cycles of therapy. Changes in ALC and uninvolved Ig were significantly different across treatments, with VCD and HD-DEX producing reductions in uninvolved Ig, and RD, VD and VRD leading to increases in uninvolved Ig. In addition, treatment with RD, VD and VRD was independently associated with higher odds of achieving a ⩾25% increase in or normalization of the primary uninvolved Ig on multivariate analysis. Although achievement of a humoral response in the primary uninvolved Ig was associated with a higher odds of achieving VGPR or better after four cycles of therapy, it was not associated with improved overall survival. These data highlight the different mechanisms of action of MM drugs and point toward a possible role for the use of VCD in treating antibody-mediated autoimmune disease.
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spelling pubmed-55844832017-09-07 Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma Ravi, P Kumar, S Gonsalves, W Buadi, F Lacy, M Q Go, R S 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 Little is known about the impact of multiple myeloma (MM) treatment on uninvolved immunoglobulins (Ig). We identified 448 patients who received high-dose dexamethasone (HD-DEX), lenalidomide and dexamethasone (RD), bortezomib and dexamethasone (VD), bortezomib, cyclophosphamide and dexamethasone (VCD) or bortezomib, lenalidomide and dexamethasone (VRD) for newly diagnosed MM at our institution between 2000 and 2013, and who had available data on absolute lymphocyte count (ALC) and quantitative uninvolved Ig at baseline and at the end of four cycles of therapy. Changes in ALC and uninvolved Ig were significantly different across treatments, with VCD and HD-DEX producing reductions in uninvolved Ig, and RD, VD and VRD leading to increases in uninvolved Ig. In addition, treatment with RD, VD and VRD was independently associated with higher odds of achieving a ⩾25% increase in or normalization of the primary uninvolved Ig on multivariate analysis. Although achievement of a humoral response in the primary uninvolved Ig was associated with a higher odds of achieving VGPR or better after four cycles of therapy, it was not associated with improved overall survival. These data highlight the different mechanisms of action of MM drugs and point toward a possible role for the use of VCD in treating antibody-mediated autoimmune disease. Nature Publishing Group 2017-06 2017-06-16 /pmc/articles/PMC5584483/ /pubmed/28622306 http://dx.doi.org/10.1038/bcj.2017.46 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 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-nc-sa/4.0/
spellingShingle Original Article
Ravi, P
Kumar, S
Gonsalves, W
Buadi, F
Lacy, M Q
Go, R S
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
Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title_full Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title_fullStr Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title_full_unstemmed Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title_short Changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
title_sort changes in uninvolved immunoglobulins during induction therapy for newly diagnosed multiple myeloma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584483/
https://www.ncbi.nlm.nih.gov/pubmed/28622306
http://dx.doi.org/10.1038/bcj.2017.46
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