# Autologous stem cell transplantation in major T‐cell lymphoma entities: An analysis by the EBMT Lymphoma Working Party

**Authors:** Evgenii Shumilov, Maud Ngoya, Philipp Berning, Irma Khvedelidze, Yasmina Serroukh, Marielle Wondergem, Kate Cwynarski, Lorenz Thurner, Björn E. Wahlin, Robert Zeiser, Carin Hazenberg, Emma Nicholson, Peter Remenyi, Tanja Netelenbos, Stig Lenhoff, Olivier Tournilhac, Keith Wilson, Aloysius Ho, Georg Lenz, Gerald Wulf, Bertram Glass, Peter Dreger, Anna Sureda, Ghandi Damaj, Ali Bazarbachi, Norbert Schmitz

PMC · DOI: 10.1002/hem3.70313 · HemaSphere · 2026-02-24

## TL;DR

This study analyzes autologous stem cell transplantation outcomes in major T-cell lymphoma types, finding better survival for ALK-negative ALCL and identifying factors like age and gender that affect results.

## Contribution

The study provides updated survival data and identifies prognostic factors for autologous stem cell transplantation in major T-cell lymphoma entities.

## Key findings

- Patients with ALK-negative ALCL had significantly better survival than those with PTCL NOS or AITL.
- Male gender, higher age, and non-CR status at auto-SCT were linked to poorer outcomes.
- Auto-SCT showed good results even in salvage settings, with 3-year OS of 59.5% for r/r patients.

## Abstract

Autologous stem cell transplantation (auto‐SCT) is an established treatment for peripheral T‐cell lymphoma (PTCL) to consolidate first remission and for patients with relapsed/refractory (r/r) disease. We aimed to examine the outcomes of patients with PTCL NOS, AITL, and ALK‐negative ALCL undergoing auto‐SCT between 2010 and 2022 and reported to EBMT. Adult patients with major T‐cell entities who had received auto‐SCT either up‐front or for r/r disease were included. 2082 patients underwent up‐front and 1249 salvage auto‐SCT. Three‐year progression‐free (PFS) and overall survival (OS) after up‐front auto‐SCT were 55.2% and 73.1%. For r/r patients, 3‐year PFS and OS were 42.6% and 59.5%. In multivariate analysis, male patients, histology other than ALK‐negative ALCL, non‐CR, and higher age at auto‐SCT showed significantly lower PFS and OS after both, up‐front and salvage auto‐SCT, mostly reflecting the higher relapse incidence for these patients. Major outcomes did not significantly change when the analyses were restricted to the patients with PET‐based response at auto‐SCT (n = 2062). Auto‐SCT demonstrated excellent outcomes when used up‐front and surprisingly good results in salvage settings. Patients with ALK‐negative ALCL survived significantly better than patients with PTCL NOS or AITL. Male gender, higher age, and non‐CR at auto‐SCT were associated with poor outcomes. Overall, auto‐SCT is a valid treatment option in T‐cell lymphoma where targeted therapies still play a limited role.

## Linked entities

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

## Full-text entities

- **Genes:** ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}
- **Diseases:** AITL (MESH:D016399), disease (MESH:D004194), PD (MESH:D010300), NRM (MESH:D003643), malignancies (MESH:D009369), SD (MESH:D012735), PTCL (MESH:D016411), toxicity (MESH:D064420), ALCL (MESH:D017728), Lymphoma (MESH:D008223), CMR (MESH:D012075), enteropathy (MESH:C538273)
- **Chemicals:** carmustine (MESH:D002330), melphalan (MESH:D008558), BuCy (-), anthracycline (MESH:D018943), busulfan (MESH:D002066), BEAM (MESH:C041191), BV (MESH:D000079963), etoposide (MESH:D005047), cytarabine (MESH:D003561), fludarabine (MESH:C024352), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930294/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930294/full.md

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Source: https://tomesphere.com/paper/PMC12930294