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. 2023 Jul;37(7):1511-1520.
doi: 10.1038/s41375-023-01924-x. Epub 2023 May 8.

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

Affiliations

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

Philipp Berning et al. Leukemia. 2023 Jul.

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.

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Conflict of interest statement

HCR received consulting and lecture fees from Abbvie, AstraZeneca, BMS, Roche, Vertex, and Merck. HCR received research funding from Gilead Pharmaceuticals and AstraZeneca. HCR is a co-founder of CDL Therapeutics GmbH. YC received consulting fees from MSD, Novartis, Incyte, BMS, Pfizer, Abbvie, Roche, Jazz, Gilead, Amgen, Astra-Zeneca, Servier; Travel support from MSD, Roche, Gilead, Amgen, Incyte, Abbvie, Janssen, Astra-Zeneca, Jazz. AS received research grants from Takeda, BMS/Celgene. AS received consulting fees from Takeda, BMS/Celgene, Novartis, Janssen, Gilead, and Sanofi. AS received honoraria from Takeda, BMS/Celgene, MSD, Janssen, Amgen, Novartis, Gilead Kite, Sanofi, Roche, and Alexion. The remaining authors declare no competing financial interests.

Figures

Fig. 1
Fig. 1. Outcomes of NKTCL patients after allo-HSCT.
Key outcome parameters for all NKTCL patients. A Cumulative incidence of disease relapse and B non-relapse mortality. C Kaplan-Meier estimates for overall survival and D progression-free survival.
Fig. 2
Fig. 2. Overall survival of NKTCL patients across selected subgroups.
Kaplan-Meier estimates for overall survival of indicated subgroups. A Patients transplanted in European or Asian centers. B PINK score groups high vs. low/intermediate. C Remission status at allo-HSCT shown as complete response (CR)/partial response (PR) vs. relapse/progressive disease (PD). D Conditioning intensity is indicated as myeloablative conditioning (MAC) and reduced-intensity conditioning (RIC).

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