TY - JOUR
T1 - Allogeneic hematopoietic stem cell transplantation for NK/T-cell lymphoma
T2 - an international collaborative analysis
AU - Berning, Philipp
AU - Schmitz, Norbert
AU - Ngoya, Maud
AU - Finel, Hervé
AU - Boumendil, Ariane
AU - Wang, Fengrong
AU - Huang, Xiao Jun
AU - Hermine, Olivier
AU - Philippe, Laure
AU - Couronné, Lucile
AU - Jaccard, Arnaud
AU - Liu, Daihong
AU - Wu, Depei
AU - Reinhardt, Hans Christian
AU - Chalandon, Yves
AU - Wagner-Drouet, Eva
AU - Kwon, Mi
AU - Zhang, Xi
AU - Carpenter, Ben
AU - Yakoub-Agha, Ibrahim
AU - Wulf, Gerald
AU - López-Jiménez, Javier
AU - Sanz, Jaime
AU - Labussière-Wallet, Hélène
AU - Shimoni, Avichai
AU - Dreger, Peter
AU - Sureda, Anna
AU - Kim, Won Seog
AU - Glass, Bertram
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/7
Y1 - 2023/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85158115877&partnerID=8YFLogxK
U2 - 10.1038/s41375-023-01924-x
DO - 10.1038/s41375-023-01924-x
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 37157017
AN - SCOPUS:85158115877
SN - 0887-6924
VL - 37
SP - 1511
EP - 1520
JO - Leukemia
JF - Leukemia
IS - 7
ER -