Outcomes of patients with HTLV-1 adult T-cell leukemia/lymphoma (ATLL) after allogeneic SCT: results of the EBMT LWP

  • Patricia López-Pereira*
  • , Ali Bazarbachi
  • , Ambroise Marçais
  • , Maud Ngoya
  • , Irma Khvedelidze
  • , Arian Laurence
  • , Victoria Potter
  • , Flore Sicre de Fontbrune
  • , Alina Daniela Tanase
  • , Lucy Cook
  • , Sridhar Chaganti
  • , Emma Nicholson
  • , Yasmina Serroukh
  • , Jennifer Clay
  • , Hélène Labussière-Wallet
  • , Fabio Ciceri
  • , Bertram Glass
  • , Olivier Hermine
  • , Anna Sureda Balari
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Adult T-cell leukemia/lymphoma (ATLL) is a rare HTLV-1-associated malignancy with a dismal prognosis due to intrinsic chemoresistance and immunosuppression. This retrospective EBMT registry analysis evaluated outcomes of allogeneic stem cell transplantation (allo-SCT) in 73 ATLL patients transplanted between 2004 and 2021. With a median follow-up of 3.9 years, 2-year overall survival (OS) and progression-free survival (PFS) were 49% (95% CI 37–60) and 43% (95% CI 31–54), respectively. Non-relapse mortality was 7% at 2 years, while relapse incidence (RI) was 49.8%. Multivariate analysis identified haploidentical donors as associated with improved OS, while non-CR status at transplant was independently associated with significantly worse PFS (HR 2.93, p = 0.01), OS (HR 4.12, p = 0.002), and RI (HR 2.66, p = 0.04) compared to CR. Our findings suggest that allo-SCT represents a feasible and potentially curative consolidation strategy for ATLL patients, with CR at transplant, younger age, and haploidentical donors being independent predictors of improved survival, supporting the importance of disease control, patient selection, and alternative donor strategies.

Original languageEnglish
JournalBone Marrow Transplantation
DOIs
Publication statusPublished - 3 Jan 2026

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© The Author(s), under exclusive licence to Springer Nature Limited 2026.

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