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Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide

Carfilzomib-lenalidomide-dexamethasone (KRd) therapy has yielded promising results in patients with newly diagnosed multiple myeloma (NDMM). Cereblon (CRBN) is the direct molecular target of lenalidomide and genetic polymorphisms in CRBN have been associated with lenalidomide efficacy. In this study...

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Autores principales: Huang, Phoebe A., Beedie, Shaunna L., Chau, Cindy H., Venzon, David J., Gere, Sheryl, Kazandjian, Dickran, Korde, Neha, Mailankody, Sham, Landgren, Ola, Figg, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795854/
https://www.ncbi.nlm.nih.gov/pubmed/31619706
http://dx.doi.org/10.1038/s41598-019-51446-9
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author Huang, Phoebe A.
Beedie, Shaunna L.
Chau, Cindy H.
Venzon, David J.
Gere, Sheryl
Kazandjian, Dickran
Korde, Neha
Mailankody, Sham
Landgren, Ola
Figg, William D.
author_facet Huang, Phoebe A.
Beedie, Shaunna L.
Chau, Cindy H.
Venzon, David J.
Gere, Sheryl
Kazandjian, Dickran
Korde, Neha
Mailankody, Sham
Landgren, Ola
Figg, William D.
author_sort Huang, Phoebe A.
collection PubMed
description Carfilzomib-lenalidomide-dexamethasone (KRd) therapy has yielded promising results in patients with newly diagnosed multiple myeloma (NDMM). Cereblon (CRBN) is the direct molecular target of lenalidomide and genetic polymorphisms in CRBN have been associated with lenalidomide efficacy. In this study, we assessed the correlation of five single nucleotide variants (SNVs) in the CRBN gene with clinical response and outcomes in patients with NDMM administered KRd therapy with lenalidomide maintenance, achieving favorable trial endpoints in a prospective Phase II study (NCT01402284). Of the observed SNVs, no associations with KRd therapy response were found in this patient cohort, although strong trends in hypoalbuminemia grade and hyperbilirubinemia grade emerged across the CRBN rs1672753 genotype (P = 0.0008) and the rs1714327 genotype (P = 0.0010), respectively. Our results do not provide conclusive support for the predictive utility of CRBN gene polymorphisms as potential biomarkers of clinical response to lenalidomide-based therapy in our patient population. However, these findings remain to be validated in prospective studies using larger patient populations.
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spelling pubmed-67958542019-10-25 Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide Huang, Phoebe A. Beedie, Shaunna L. Chau, Cindy H. Venzon, David J. Gere, Sheryl Kazandjian, Dickran Korde, Neha Mailankody, Sham Landgren, Ola Figg, William D. Sci Rep Article Carfilzomib-lenalidomide-dexamethasone (KRd) therapy has yielded promising results in patients with newly diagnosed multiple myeloma (NDMM). Cereblon (CRBN) is the direct molecular target of lenalidomide and genetic polymorphisms in CRBN have been associated with lenalidomide efficacy. In this study, we assessed the correlation of five single nucleotide variants (SNVs) in the CRBN gene with clinical response and outcomes in patients with NDMM administered KRd therapy with lenalidomide maintenance, achieving favorable trial endpoints in a prospective Phase II study (NCT01402284). Of the observed SNVs, no associations with KRd therapy response were found in this patient cohort, although strong trends in hypoalbuminemia grade and hyperbilirubinemia grade emerged across the CRBN rs1672753 genotype (P = 0.0008) and the rs1714327 genotype (P = 0.0010), respectively. Our results do not provide conclusive support for the predictive utility of CRBN gene polymorphisms as potential biomarkers of clinical response to lenalidomide-based therapy in our patient population. However, these findings remain to be validated in prospective studies using larger patient populations. Nature Publishing Group UK 2019-10-16 /pmc/articles/PMC6795854/ /pubmed/31619706 http://dx.doi.org/10.1038/s41598-019-51446-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Phoebe A.
Beedie, Shaunna L.
Chau, Cindy H.
Venzon, David J.
Gere, Sheryl
Kazandjian, Dickran
Korde, Neha
Mailankody, Sham
Landgren, Ola
Figg, William D.
Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title_full Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title_fullStr Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title_full_unstemmed Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title_short Cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
title_sort cereblon gene variants and clinical outcome in multiple myeloma patients treated with lenalidomide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795854/
https://www.ncbi.nlm.nih.gov/pubmed/31619706
http://dx.doi.org/10.1038/s41598-019-51446-9
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