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Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma

BACKGROUND: The purpose of this study was to examine the factors associated with disparities in overall survival (OS) by race in pediatric diffuse large B‐cell lymphoma (DLBCL) patients. METHODS: We evaluated clinical features and survival among patients ≤21 years of age diagnosed with stage I–IV DL...

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Autores principales: Khullar, Karishma, Plascak, Jesse J., Drachtman, Richard, Cole, Peter D., Parikh, Rahul R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926019/
https://www.ncbi.nlm.nih.gov/pubmed/33503323
http://dx.doi.org/10.1002/cam4.3736
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author Khullar, Karishma
Plascak, Jesse J.
Drachtman, Richard
Cole, Peter D.
Parikh, Rahul R.
author_facet Khullar, Karishma
Plascak, Jesse J.
Drachtman, Richard
Cole, Peter D.
Parikh, Rahul R.
author_sort Khullar, Karishma
collection PubMed
description BACKGROUND: The purpose of this study was to examine the factors associated with disparities in overall survival (OS) by race in pediatric diffuse large B‐cell lymphoma (DLBCL) patients. METHODS: We evaluated clinical features and survival among patients ≤21 years of age diagnosed with stage I–IV DLBCL from 2004 to 2014 from the National Cancer Database (NCDB) using a multivariable Cox proportional hazards model. RESULTS: Among 1386 pediatric patients with DLBCL, 1023 patients met eligibility criteria. In unadjusted analysis, Black patients had a significantly higher overall death rate than White patients (HR(Black vs. White) 1.51; 95% CI: 1.02–2.23, p = 0.041). The survival disparity did not remain significant in adjusted analysis, though controlling for covariates had little effect on the magnitude of the disparity (HR 1.46; 95% CI 0.93–2.31, p = 0.103). In adjusted models, presence of B symptoms, receipt of chemotherapy, stage of disease, and Other insurance were significantly associated with OS. Specifically, patients with B symptoms and those with Other insurance were more likely to die than those without B symptoms or private insurance, respectively (HR 1.75; 95% CI 1.22–2.50, p = 0.002) and (HR 2.56; 95% CI, 1.39–4.73, p = 0.0027), patients who did not receive chemotherapy were three times more likely to die than those who received chemotherapy (HR 3.10; CI 1.80–5.35, p < 0.001), and patients who presented with earlier stage disease were less likely to die from their disease than those with stage IV disease (stages I–III HR 0.34, CI 0.18–0.64, p < 0.001; HR 0.50, CI 0.30–0.82, p = 0.006, HR 0.72, CI 0.43–1.13, p = 0.152, respectively). CONCLUSIONS: Our results suggest that racial disparities in survival may be mediated by clinical and treatment parameters.
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spelling pubmed-79260192021-03-12 Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma Khullar, Karishma Plascak, Jesse J. Drachtman, Richard Cole, Peter D. Parikh, Rahul R. Cancer Med Clinical Cancer Research BACKGROUND: The purpose of this study was to examine the factors associated with disparities in overall survival (OS) by race in pediatric diffuse large B‐cell lymphoma (DLBCL) patients. METHODS: We evaluated clinical features and survival among patients ≤21 years of age diagnosed with stage I–IV DLBCL from 2004 to 2014 from the National Cancer Database (NCDB) using a multivariable Cox proportional hazards model. RESULTS: Among 1386 pediatric patients with DLBCL, 1023 patients met eligibility criteria. In unadjusted analysis, Black patients had a significantly higher overall death rate than White patients (HR(Black vs. White) 1.51; 95% CI: 1.02–2.23, p = 0.041). The survival disparity did not remain significant in adjusted analysis, though controlling for covariates had little effect on the magnitude of the disparity (HR 1.46; 95% CI 0.93–2.31, p = 0.103). In adjusted models, presence of B symptoms, receipt of chemotherapy, stage of disease, and Other insurance were significantly associated with OS. Specifically, patients with B symptoms and those with Other insurance were more likely to die than those without B symptoms or private insurance, respectively (HR 1.75; 95% CI 1.22–2.50, p = 0.002) and (HR 2.56; 95% CI, 1.39–4.73, p = 0.0027), patients who did not receive chemotherapy were three times more likely to die than those who received chemotherapy (HR 3.10; CI 1.80–5.35, p < 0.001), and patients who presented with earlier stage disease were less likely to die from their disease than those with stage IV disease (stages I–III HR 0.34, CI 0.18–0.64, p < 0.001; HR 0.50, CI 0.30–0.82, p = 0.006, HR 0.72, CI 0.43–1.13, p = 0.152, respectively). CONCLUSIONS: Our results suggest that racial disparities in survival may be mediated by clinical and treatment parameters. John Wiley and Sons Inc. 2021-01-27 /pmc/articles/PMC7926019/ /pubmed/33503323 http://dx.doi.org/10.1002/cam4.3736 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Khullar, Karishma
Plascak, Jesse J.
Drachtman, Richard
Cole, Peter D.
Parikh, Rahul R.
Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title_full Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title_fullStr Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title_full_unstemmed Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title_short Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
title_sort associations between race and survival in pediatric patients with diffuse large b‐cell lymphoma
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926019/
https://www.ncbi.nlm.nih.gov/pubmed/33503323
http://dx.doi.org/10.1002/cam4.3736
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