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Survival Disparities of Diffuse Large B-Cell Lymphoma in a Community-Based Inner-City Cancer Center
被引:3
|作者:
Tiu, Andrew
[1
]
Jorge, Vinicius
[2
]
Moussa, Peter
[1
]
Djibo, Djeneba Audrey
[3
]
Gupta, Sorab
[2
]
Alpdogan, Onder
[4
]
Dourado, Claudia
[2
]
机构:
[1] Einstein Med Ctr, Dept Med, 5501 Old York Rd, Philadelphia, PA 19141 USA
[2] Einstein Med Ctr, Div Hematol & Med Oncol, Philadelphia, PA 19141 USA
[3] Einstein Med Ctr, Div Res, Dept Med, Philadelphia, PA 19141 USA
[4] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Med Oncol, Div Hematol Malignancies & Hematopoiet Stem Cell, Philadelphia, PA 19107 USA
来源:
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA
|
2021年
/
21卷
/
04期
关键词:
African Americans;
Blacks;
NON-HODGKIN-LYMPHOMA;
RACIAL-DIFFERENCES;
CLASSIFICATION;
D O I:
10.1016/j.clml.2020.10.003
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
There are persistent racial disparities in survival among patients with diffuse large B-cell lymphoma (DLBCL). We conducted a cohort study of 181 patients for 10 years in a single community-based inner-city cancer center. Blacks had decreased overall survival compared to non-Blacks even after excluding patients with HIV and who did not receive chemotherapy. Revised International Prognostic Index score alone could not predict worse outcomes and increased mortality in Blacks with DLBCL. Background: Diffuse large B-cell lymphoma (DLBCL) comprises approximately 30% of all non-Hodgkin lymphomas. Multiple studies have demonstrated race-based disparities in survival among patients with DLBCL across all stages of disease, in the era both before and after rituximab. The etiology for the racial disparities in survival among patients with DLBCL is still unknown. Moreover, the Revised International Prognostic Index (R-IPI), a tool that predicts the DLBCL patients' outcome, has not yet been validated in African Americans (AA). Patients and Methods: We conducted a cohort study of patients diagnosed with DLBCL from January 1, 2007, to December 31, 2017, from our tumor registry in a single community-based inner-city cancer center. We abstracted demographic, clinical, histopathologic, treatment, and R-IPI variables. A total of 181 patients (47.5%) with biopsy-proven DLBCL were included in the retrospective analysis. The median age was 65 years, 47% were men, 41% were AA, and 44% were white. Results: The AA group had a younger median age, higher lactate dehydrogenase levels, higher frequency of B symptoms, and higher HIV infection than the non-AA group. The AA group had significantly decreased median overall survival than the nonAA group (15.7 months; 95% confidence interval, 10.3 to 23.9, vs. 93.6 months; 95% confidence interval, 61.5 to 142.6, respectively; P < .001). The survival disparities persisted after excluding patients with HIV and who did not receive chemotherapy. In addition, AA race predicts a reduced survival by univariate and multivariate analysis. Conclusion: AA with DLBCL may have a poorer prognosis than the non-AA population. Further studies should investigate the biology of DLBCL in the AA population. (C) 2020 Elsevier Inc. All rights reserved.
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页码:205 / 215
页数:11
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