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Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis

Findings on racial differences in survival in multiple myeloma (MM) have been inconclusive. We assessed differences in outcomes between White and Black individuals among 639 newly diagnosed MM patients in the MM Research Foundation CoMMpass registry with baseline cytogenetic data. Survival curves we...

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Autores principales: Derman, Benjamin A., Jasielec, Jagoda, Langerman, Spencer S., Zhang, Wei, Jakubowiak, Andrzej J., Chiu, Brian C.-H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414120/
https://www.ncbi.nlm.nih.gov/pubmed/32770051
http://dx.doi.org/10.1038/s41408-020-00347-6
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author Derman, Benjamin A.
Jasielec, Jagoda
Langerman, Spencer S.
Zhang, Wei
Jakubowiak, Andrzej J.
Chiu, Brian C.-H.
author_facet Derman, Benjamin A.
Jasielec, Jagoda
Langerman, Spencer S.
Zhang, Wei
Jakubowiak, Andrzej J.
Chiu, Brian C.-H.
author_sort Derman, Benjamin A.
collection PubMed
description Findings on racial differences in survival in multiple myeloma (MM) have been inconclusive. We assessed differences in outcomes between White and Black individuals among 639 newly diagnosed MM patients in the MM Research Foundation CoMMpass registry with baseline cytogenetic data. Survival curves were constructed using the Kaplan–Meier method. Hazard ratios and 95% confidence intervals were derived from Cox proportional hazard regression models. Age, gender, and stage were similar between Whites (n = 526) and Blacks (n = 113). Blacks had inferior overall survival (OS) compared with Whites and were less likely to receive triplet therapies or frontline autologous stem cell transplant (ASCT). The following factors were significantly associated with inferior OS in multivariate analysis: higher international staging system (ISS) score, ≥1 or ≥2 high-risk cytogenetic abnormalities (HRCA), high-risk gene expression profile (GEP), and lack of ASCT. Multivariate analysis in the Black subset found that only lack of ASCT was significantly associated with inferior OS. The receipt of both triplet induction and ASCT only partly abrogated the effect of race on survival. HRCA did not track with survival in Blacks, emphasizing the need for race-specific risk prognostication schema to guide optimal MM therapy.
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spelling pubmed-74141202020-08-14 Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis Derman, Benjamin A. Jasielec, Jagoda Langerman, Spencer S. Zhang, Wei Jakubowiak, Andrzej J. Chiu, Brian C.-H. Blood Cancer J Article Findings on racial differences in survival in multiple myeloma (MM) have been inconclusive. We assessed differences in outcomes between White and Black individuals among 639 newly diagnosed MM patients in the MM Research Foundation CoMMpass registry with baseline cytogenetic data. Survival curves were constructed using the Kaplan–Meier method. Hazard ratios and 95% confidence intervals were derived from Cox proportional hazard regression models. Age, gender, and stage were similar between Whites (n = 526) and Blacks (n = 113). Blacks had inferior overall survival (OS) compared with Whites and were less likely to receive triplet therapies or frontline autologous stem cell transplant (ASCT). The following factors were significantly associated with inferior OS in multivariate analysis: higher international staging system (ISS) score, ≥1 or ≥2 high-risk cytogenetic abnormalities (HRCA), high-risk gene expression profile (GEP), and lack of ASCT. Multivariate analysis in the Black subset found that only lack of ASCT was significantly associated with inferior OS. The receipt of both triplet induction and ASCT only partly abrogated the effect of race on survival. HRCA did not track with survival in Blacks, emphasizing the need for race-specific risk prognostication schema to guide optimal MM therapy. Nature Publishing Group UK 2020-08-07 /pmc/articles/PMC7414120/ /pubmed/32770051 http://dx.doi.org/10.1038/s41408-020-00347-6 Text en © The Author(s) 2020 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
Derman, Benjamin A.
Jasielec, Jagoda
Langerman, Spencer S.
Zhang, Wei
Jakubowiak, Andrzej J.
Chiu, Brian C.-H.
Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title_full Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title_fullStr Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title_full_unstemmed Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title_short Racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
title_sort racial differences in treatment and outcomes in multiple myeloma: a multiple myeloma research foundation analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414120/
https://www.ncbi.nlm.nih.gov/pubmed/32770051
http://dx.doi.org/10.1038/s41408-020-00347-6
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