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Associations between race and survival in pediatric patients with diffuse large B‐cell lymphoma
Author(s) -
Khullar Karishma,
Plascak Jesse J.,
Drachtman Richard,
Cole Peter D.,
Parikh Rahul R.
Publication year - 2021
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.3736
Subject(s) - medicine , stage (stratigraphy) , proportional hazards model , chemotherapy , diffuse large b cell lymphoma , lymphoma , cancer , survival analysis , disease , paleontology , biology
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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