Autologous stem cell transplantation in T-cell/histiocyte-rich large B-cell lymphoma: EBMT Lymphoma Working Party study.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
30 Aug 2024
Historique:
accepted: 05 08 2024
received: 12 03 2024
revised: 29 07 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 30 8 2024
Statut: aheadofprint

Résumé

Although broadly employed, consolidative autologous hematopoietic stem cell transplantation (autoHCT) for relapsed/refractory (r/r) T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) has never been specifically investigated. Here we have analyzed outcomes of autoHCT for THRLBCL compared to diffuse large cell B-cell lymphoma not otherwise specified (DLBCL). Eligible for this retrospective registry study were adult patients with r/r THRLBCL and DLBCL, respectively, who underwent a first autoHCT in a salvage-sensitive disease status as assessed by PET-CT between 2016 and 2021 and were registered with the European Society for Blood and Marrow Transplantation (EBMT) database. Primary endpoint was progression-free survival (PFS) 2 years after transplantation. Two-hundred-one patients with THRLBCL and 5,543 with DLBCL were included. There were no significant differences in terms of disease status at HCT, pretreatment lines, and interval from diagnosis to transplant between the cohorts, but patients with THRBCL were significantly younger, contained a higher proportion of men, and had a better performance status. Compared to DLBCL, THRLBCL was associated with significantly better 2-year PFS (78% vs. 59%; p<0.001) and overall survival (OS; 81% vs. 74%; p=0.02) because of a significantly lower 2-year relapse incidence (RI; 16% vs. 35%; p<0.001). On multivariate analysis, favorable relapse risk (hazard ratio (HR) 0.46, 95%CI 0.31-0.7) and PFS (HR 0.58, 95%CI 0.41-0.82) of patients with THRLBCL remained significant, while OS benefits (HR 0.78, 95%CI 0.54-1.12) did not. These results were validated in a propensity-score matched analysis. These data prove autoHCT as an effective treatment option for salvage-sensitive r/r THRLBCL.

Identifiants

pubmed: 39213423
pii: 517647
doi: 10.1182/bloodadvances.2024013152
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Simon Renders (S)

Heidelberg University Hospital, Department of Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg, Germany.

Marie-Thérèse Rubio (MT)

CHRU Nancy, Vandoeuvre les Nancy, France.

William M Townsend (WM)

University College London Hospitals, London, United Kingdom.

Roland Schroers (R)

Ruhr-Universität Bochum, Bochum, Germany.

Urban Novak (U)

Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Nicolaas Schaap (N)

Radboud University Medical Centre Nijmegen, Nijmegen, Netherlands.

Mahmoud Aljurf (M)

King Faisal Specialist Hospital, Riyadh, Saudi Arabia.

Grzegorz Helbig (G)

Silesian Medical University, Katowice, Poland.

Matthew Collin (M)

Newcastle University, Newcastle Upon Tyne, United Kingdom.

Guido Kobbe (G)

Heinrich Heine University, Medical Faculty, Duesseldorf, Germany.

Huynh Anne (H)

CHU de Toulouse, Toulouse, France.

José Antonio Antonio Pérez-Simón (JAA)

Universidad de Sevilla, Spain.

Adrian Bloor (A)

Christie NHS Trust Hospital, Manchester, United Kingdom.

Hervé Ghesquieres (H)

Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre-Benite, France.

Anna Sureda (A)

Institut Català d'Oncologia, Barcelona, Spain.

Norbert Schmitz (N)

University Hospital Muenster Germany, Muenster, Germany.

Bertram Glass (B)

Helios Klinikum Berlin-Buch, Berlin, Germany.

Peter Dreger (P)

University of Heidelberg, Heidelberg, Germany.

Classifications MeSH