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Allogeneic hematopoietic stem cell transplantation for NK/T-cell lymphoma: an international collaborative analysis

  • Philipp Berning
  • , Norbert Schmitz
  • , Maud Ngoya
  • , Hervé Finel
  • , Ariane Boumendil
  • , Fengrong Wang
  • , Xiao Jun Huang
  • , Olivier Hermine
  • , Laure Philippe
  • , Lucile Couronné
  • , Arnaud Jaccard
  • , Daihong Liu
  • , Depei Wu
  • , Hans Christian Reinhardt
  • , Yves Chalandon
  • , Eva Wagner-Drouet
  • , Mi Kwon
  • , Xi Zhang
  • , Ben Carpenter
  • , Ibrahim Yakoub-Agha
  • Gerald Wulf, Javier López-Jiménez, Jaime Sanz, Hélène Labussière-Wallet, Avichai Shimoni, Peter Dreger, Anna Sureda, Won Seog Kim, Bertram Glass
  • University of Münster
  • Sorbonne Université
  • Peking University
  • Université Paris Cité
  • CHU Dupuytren
  • General Hospital of People’s Liberation Army
  • The First Affiliated Hospital of Soochow University
  • University of Duisburg-Essen
  • University of Geneva
  • Johannes Gutenberg University Mainz
  • Hospital General Universitario Gregorio Marañon
  • Chongqing Medical University
  • University College London Hospitals NHS Foundation Trust
  • Université de Lille
  • University of Göttingen
  • Hospital Ramon y Cajal
  • Hospital Universitario La Fe
  • Hospices civils de Lyon
  • Sheba Medical Center at Tel Hashomer
  • Heidelberg University 
  • University of Barcelona
  • Helios Clinic

Research output: Contribution to journal › Article › peer-review

Abstract

Natural killer/T-cell lymphomas (NKTCL) represent rare and aggressive lymphoid malignancies. Patients (pts) with relapsed/refractory disease after Asparaginase (ASPA)-based chemotherapy have a dismal prognosis. To better define the role of allogeneic hematopoietic stem cell transplantation (allo-HSCT), we conducted a retrospective analysis of data shared with the European Society for Blood and Marrow Transplantation (EBMT) and cooperating Asian centers. We identified 135 pts who received allo-HSCT between 2010 and 2020. Median age was 43.4 years at allo-HSCT, 68.1% were male. Ninety-seven pts (71.9 %) were European, 38 pts (28.1%) Asian. High Prognostic Index for NKTCL (PINK) scores were reported for 44.4%; 76.3% had >1 treatment, 20.7% previous auto-HSCT, and 74.1% ASPA-containing regimens prior to allo-HSCT. Most (79.3%) pts were transplanted in CR/PR. With a median follow-up of 4.8 years, 3-year progression-free(PFS) and overall survival were 48.6% (95%-CI:39.5–57%) and 55.6% (95%-CI:46.5–63.8%). Non-relapse mortality at 1 year was 14.8% (95%-CI:9.3–21.5%) and 1-year relapse incidence 29.6% (95%-CI:21.9–37.6%). In multivariate analyses, shorter time interval (0–12 months) between diagnosis and allo-HSCT [HR = 2.12 (95%-CI:1.03–4.34); P = 0.04] and transplantation not in CR/PR [HR = 2.20 (95%-CI:0.98–4.95); P = 0.056] reduced PFS. Programmed cell death protein 1(PD-1/PD-L1) treatment before HSCT neither increased GVHD nor impacted survival. We demonstrate that allo-HSCT can achieve long-term survival in approximately half of pts allografted for NKTCL.

Original languageEnglish
Pages (from-to)1511-1520
Number of pages10
JournalLeukemia
Volume37
Issue number7
DOIs
StatePublished - Jul 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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