Primary renal lymphoma: A population-based analysis using the SEER program (1973-2015)
Alankrita Taneja1, Vivek Kumar2,3, Abhinav B Chandra4
1Department of Internal Medicine, Wayne State University School of Medicine, Detroit, MI, USA.
European Journal of Haematology
|November 27, 2019
Summary
Primary renal lymphoma (PRL) is a rare kidney cancer with increasing incidence. Older age is a risk factor for worse survival, while non-diffuse large B-cell lymphoma (DLBCL) histology is linked to better outcomes.
Area of Science:
- Oncology
- Epidemiology
- Pathology
Background:
- Primary renal lymphoma (PRL) is a rare non-Hodgkin lymphoma (NHL) confined to the kidneys.
- Existing literature on PRL epidemiology and outcomes is limited.
Observation:
- Utilized the Surveillance, Epidemiology, and End Result (SEER) database (1984-2015) to analyze PRL characteristics.
- Identified 599 eligible PRL patients, representing 0.17% of all NHL cases.
- Observed an increasing age-adjusted incidence of PRL.
Findings:
- The median age of PRL patients was 72 years, with a predominance of Caucasian males.
- Diffuse large B-cell lymphoma (DLBCL) was the most common histologic type, often presenting as unilateral tumors.
- Age 60 years or older was the strongest predictor of worse overall survival (OS) and cause-specific survival (CSS).
- Non-DLBCL histology was associated with improved OS and CSS.
Implications:
- PRL is a rare entity with a rising incidence.
- Age and specific lymphoma subtypes significantly impact patient survival.
- Further research into PRL is warranted given its rarity and evolving incidence patterns.
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