» Articles » PMID: 33745341

Myeloablative Haploidentical Transplant As an Alternative to Matched Sibling Transplant for Peripheral T-Cell Lymphomas

Overview
Journal Cell Transplant
Date 2021 Mar 22
PMID 33745341
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

The number of HLA-haploidentical allogeneic hematopoietic stem-cell transplantation (Haplo-HSCT) is increasing. Comparative studies about Haplo-HSCT versus allo-HSCT with HLA-matched sibling donors (MSD-HSCT) have been tried in leukemias and B-cell lymphomas. Few studies were reported in Peripheral T-cell lymphomas (PTCLs). We performed a multicenter retrospective study about 52 patients with PTCLs undergoing Haplo-HSCT ( = 20) or MSD-HSCT ( = 32). All Haplo-HSCT recipients received antithymocyte globulin (ATG) based graft versus host disease (GVHD) prophylaxis. The median follow-up for all survivors was 38 months. The 100-day cumulative incidence of grade II to IV acute GVHD was similar (19% in the MSD-HSCT group versus 28% in the Haplo-HSCT group, 0.52). The 2-year cumulative incidence of chronic GVHD (limited and extensive) after Haplo-HSCT (30%) was also similar with that in the MSD-HSCT group (50%, 0.15). The 3-year relapse rates (33% vs 27%, 0.84) and non-relapse mortality (21% vs 22%, 0.78) did not differ between these two groups. There were also no differences in 3-year overall survival (OS) (48% vs 50%, 0.78) and progression-free survival (47% vs 51%, 0.95) between these two groups. On multivariate analysis, prognostic index for T-cell lymphoma (PIT) score (higher than 1: hazard ratio [HR], 4.0; 0.003) and disease status (stable or progression disease before HSCT: HR, 2.8; 0.03) were independent variables associated with worse OS. We concluded that ATG-based haplo-HSCT platform could work as an alternative to MSD-HSCT for patients with PTCLs.

Citing Articles

Outcome of allogeneic transplantation for mature T-cell lymphomas: impact of donor source and disease characteristics.

Hamadani M, Ngoya M, Sureda A, Bashir Q, Litovich C, Finel H Blood Adv. 2021; 6(3):920-930.

PMID: 34861680 PMC: 8945300. DOI: 10.1182/bloodadvances.2021005899.

References
1.
Chen H, Liu K, Xu L, Chen Y, Han W, Zhang X . Haploidentical hematopoietic stem cell transplantation without in vitro T cell depletion for the treatment of philadelphia chromosome-positive acute lymphoblastic leukemia. Biol Blood Marrow Transplant. 2015; 21(6):1110-6. DOI: 10.1016/j.bbmt.2015.02.009. View

2.
Kwong Y, Anderson B, Advani R, Kim W, Levine A, Lim S . Management of T-cell and natural-killer-cell neoplasms in Asia: consensus statement from the Asian Oncology Summit 2009. Lancet Oncol. 2009; 10(11):1093-101. DOI: 10.1016/S1470-2045(09)70265-7. View

3.
Wang Y, Wang H, Lai Y, Sun Z, Wu D, Jiang M . Haploidentical transplant for myelodysplastic syndrome: registry-based comparison with identical sibling transplant. Leukemia. 2016; 30(10):2055-2063. DOI: 10.1038/leu.2016.110. View

4.
Przepiorka D, Weisdorf D, MARTIN P, Klingemann H, Beatty P, Hows J . 1994 Consensus Conference on Acute GVHD Grading. Bone Marrow Transplant. 1995; 15(6):825-8. View

5.
Wang Y, Liu D, Xu L, Liu K, Chen H, Chen Y . Superior graft-versus-leukemia effect associated with transplantation of haploidentical compared with HLA-identical sibling donor grafts for high-risk acute leukemia: an historic comparison. Biol Blood Marrow Transplant. 2010; 17(6):821-30. DOI: 10.1016/j.bbmt.2010.08.023. View