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. 2025 Jul;207(1):132-140.
doi: 10.1111/bjh.20132. Epub 2025 May 6.

Distinct characteristics and social determinants in adult T-cell leukaemia/lymphoma patients at a tertiary cancer centre in Canada

Affiliations

Distinct characteristics and social determinants in adult T-cell leukaemia/lymphoma patients at a tertiary cancer centre in Canada

Tomohiro Aoki et al. Br J Haematol. 2025 Jul.

Abstract

Adult T-cell leukaemia/lymphoma (ATLL) is a rare, aggressive haematological malignancy linked to human T-cell leukaemia virus type I (HTLV-1) and associated with poor outcomes. Despite its higher prevalence in HTLV-1-endemic regions, the relationship between clinical characteristics and patients' sociocultural background remains underexplored. We retrospectively analysed 79 ATLL patients treated at our institution (1993-2023). The median age at diagnosis was 47 years, and 72% of patients were of Caribbean origin. Median progression-free and overall survival were 10.2 and 16.2 months, respectively, with only five patients receiving allogeneic stem cell transplantation. Central nervous system (CNS) involvement at diagnosis occurred in 22% of patients and was associated with worse outcomes, while 14% experienced CNS relapse within a median of 4.9 months. Using the Ontario Marginalization Index, we found higher levels of material, household/dwelling and racialized/newcomer-related marginalization compared to the general Greater Toronto Area population, though these factors were not linked to poorer outcomes. Our findings reveal that ATLL patients in this cohort were predominantly of Caribbean descent, presented at a young age and faced significant CNS involvement and poor survival outcomes, underscoring ATLL as an unmet clinical need.

Keywords: HTLV‐1; adult T‐cell leukaemia/lymphoma (ATLL); central nervous system involvement; haematological malignancy; health disparities; retrospective cohort.

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Conflict of interest statement

The authors declare that there are no conflicts of interest related to the work presented in this manuscript.

Figures

FIGURE 1
FIGURE 1
(A) Progression‐free survival (PFS) and (B) overall survival (OS) of the entire study cohort.
FIGURE 2
FIGURE 2
(A) Progression‐free survival (PFS) of the study cohort according to CNS involvement at diagnosis. (B) Cumulative incidence of CNS relapse of the study cohort. (C) The alluvial plot shows the ethnicity of the study cohort and CNS involvement status at diagnosis and relapse. Horizontal ribbons represent individual cases and can be followed from left to right. CNS, central nervous system.
FIGURE 3
FIGURE 3
(A) Density plot showing factor scores of four different dimensions of marginalization (higher scores represent increased marginalization). (B) Progression‐free survival of the study cohort according to the deprivation indices.

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