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Br J Haematol ; 204(6): 2222-2226, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38420697

ABSTRACT

To address the lack of contemporary population-based epidemiological studies of hepatosplenic T-cell lymphoma (HSTCL), we undertook a population-based study of ICD-O-3-coded HSTCL in England. We used the National Cancer Registration Dataset and linked datasets on hospital admissions, Systemic Anti-Cancer Therapy, socio-demographics, comorbidities and death, identifying cases from 1 January 2013 to 31 December 2019 with survival data up to 5 January 2021. Crude and directly age-standardised incidence rates per million persons per year were calculated. Crude and adjusted incidence rate ratios compared incidence between groups using Poisson regression. A Cox proportional hazards model estimated mortality risks adjusted for age, sex, ethnicity, deprivation and allogenic stem cell transplant (allo-SCT; time varying). We identified 44 patients, mean age 42 years. Median survival was 11 months, and 1 and 5 year survivals were 48% (95% CI 29%-43%) and 22% (95% CI 12%-42%) respectively. The age-standardised incidence was 0.1 per million/year. Incidence was higher in areas with greater deprivation (0.15 per million/year), and more cases than expected were in non-White patients (39%). Non-Whites had a twofold increased risk of death (adjusted hazard ratio 2.21 [95% CI 1.03-4.78]) even after adjusting for deprivation, younger age and allo-SCT. In conclusion, ethnicity and socio-economic status affect both the incidence and survival of HSTCL.


Subject(s)
Lymphoma, T-Cell , Splenic Neoplasms , Humans , Male , Female , Incidence , Adult , Middle Aged , Lymphoma, T-Cell/mortality , Lymphoma, T-Cell/epidemiology , Lymphoma, T-Cell/therapy , Splenic Neoplasms/mortality , Splenic Neoplasms/epidemiology , Aged , Liver Neoplasms/mortality , Liver Neoplasms/epidemiology , Liver Neoplasms/therapy , Social Class , Ethnicity/statistics & numerical data , England/epidemiology , Young Adult , Adolescent
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