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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6795854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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