# Allogeneic stem cell transplantation for major T-cell lymphoma entities: an analysis of the EBMT-lymphoma working party

**Authors:** Evgenii Shumilov, Maud Ngoya, Philipp Berning, Raynier Devillier, Edouard Forcade, Thomas Schroeder, Frank Kroschinsky, Matthias Stelljes, Veronika Valkova, Francesca Kinsella, Patrice Chevallier, Gitte Olesen, Mohamad Mohty, Flore Sicre de Fontbrune, Eva Wagner-Drouet, Robert Zeiser, Marco Herling, Georg-Nikolaus Franke, Lucía López-Corral, Francis Ayuk, Georg Lenz, Gerald Wulf, Anna Sureda, Arain Laurence, Peter Dreger, Ali Bazarbachi, Norbert Schmitz

PMC · DOI: 10.1186/s13045-026-01783-w · Journal of Hematology & Oncology · 2026-02-21

## TL;DR

This study analyzes allogeneic stem cell transplantation outcomes in T-cell lymphoma patients, finding that AITL patients have better survival rates compared to others.

## Contribution

The study provides new insights into the impact of histology, disease status, and donor choice on outcomes in major T-cell lymphoma subtypes following allogeneic stem cell transplantation.

## Key findings

- Patients with angioimmunoblastic T-cell lymphoma (AITL) had significantly better survival rates compared to PTCL NOS or ALK-negative ALCL.
- Achieving complete response at transplantation was associated with improved progression-free and overall survival.
- Allogeneic stem cell transplantation remains a valid treatment option for relapsed/refractory T-cell lymphoma despite limited targeted therapies.

## Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is an established treatment for peripheral T-cell lymphoma (PTCL), particularly for patients with relapsed/refractory (r/r) disease. We aimed to retrieve novel information on the role of histology, disease status prior to transplantation, and donor choice for patients with PTCL not otherwise specified (NOS), angioimmunoblastic T-cell lymphoma (AITL), and anaplastic lymphoma kinase (ALK)-negative ALCL. We compared imaging by computed tomography (CT) or positron emission tomography (PET) for defining disease status prior to allo-SCT.

Eligible were adult patients with PTCL-NOS, AITL, and ALK-negative ALCL undergoing allo-SCT between 2010 and 2022 and reported to EBMT.

1958 patients underwent allo-SCT. Of patients with known number of prior lines of therapies (n = 1310), 301 (23%), 431 (32.9%) and 578 (44.1%) patients received allo-SCT after one (1L), two (2L) or three or more therapy lines (3L +), respective. Three-year GvHD-free, relapse-free survival (GRFS), progression-free survival (PFS) and overall survival (OS) were 35.8%, 50.9% and 56.8%, respectively. Three-year relapse incidence (RI) and non-relapse mortality were 25.1% and 24.1%, respectively. In multivariate analysis, histology other than AITL, no complete response (CR) at transplantation, having a haploidentical donor and higher age at allo-SCT resulted in significantly lower PFS and/or OS. Prior autologous SCT had no impact on the results of allo-SCT and major outcomes did not significantly change when the analyses were restricted to the patients with PET-based response at allo-SCT. Patients allografted in partial response (PR) or SD/PD still achieved long-term survival with a 3-year PFS/OS of 46%/53.7% and 39.6%/43.6%, respectively.

Allo-SCT is a valid treatment option in relapsed/refractory PTCL where targeted therapies still play a limited role. Patients with AITL survived significantly better than patients with PTCL NOS or ALK-negative ALCL following a significantly lower RI, also when comparing CR/complete metabolic response (CMR) and PR patients separately. Higher age and non-CR at allo-SCT are associated with worse outcomes.

The online version contains supplementary material available at 10.1186/s13045-026-01783-w.

## Linked entities

- **Diseases:** peripheral T-cell lymphoma (MONDO:0000430), angioimmunoblastic T-cell lymphoma (MONDO:0004977)

## Full-text entities

- **Genes:** ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}
- **Diseases:** CR (MESH:D001766), non (MESH:C580335), chronic graft-versus-host disease (MESH:D000092122), ALCL (MESH:D017728), TBI (MESH:D000070642), Graft-versus-host disease (MESH:D006086), PTCL (MESH:D016411), SD (MESH:D012735), stable disease (MESH:D060050), malignancies (MESH:D009369), PD (MESH:D010300), MAC (MESH:D020763), cGvHD (MESH:D002908), infectious complications (MESH:D003141), aggressive (MESH:D010554), Lymphoma (MESH:D008223), toxicity (MESH:D064420), Death (MESH:D003643), , non-leukemic T-cell lymphoma (MESH:D016399), NOS (MESH:C536665)
- **Chemicals:** cyclophosphamide (MESH:D003520), MTX (MESH:D008727), BV (MESH:D000079963), MMF (MESH:D009173), carmustine (MESH:D002330), cytarabine (MESH:D003561), etoposide (MESH:D005047), BEAM (MESH:C041191), BU (MESH:D002066), CSA (MESH:D016572), PTCY (-), melphalan (MESH:D008558)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930567/full.md

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Source: https://tomesphere.com/paper/PMC12930567