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

Author:

Zhenyang Gu1ORCID,Nainong Li2,Xiaoxiong Wu3,Maihong Wang4,Xiaorui Fu5,Zhao Wang6,Hanyun Ren7,Yuhang Li8,Xiaofan Li2ORCID,Yamei Wu3,Yao Liu4,Mingzhi Zhang5,Yini Wang6,Daihong Liu1,Yujun Dong7,Liangding Hu8,Wenrong Huang1

Affiliation:

1. Department of Hematology, Chinese PLA General Hospital, Beijing, China

2. Department of Hematology, Fujian Institute of Hematology, Fuzhou, China

3. Department of Hematology, The Forth Medical Center of PLA General Hospital, Beijing, China

4. Center of Hematology, Xinqiao Hospital, Third Military Medical University, Chongqing, China

5. Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

6. Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, China

7. Department of Hematology, Peking University First Hospital, Beijing, China

8. Department of Hematology, The Fifth Medical Center of PLA General Hospital, Beijing, China

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 ( n = 20) or MSD-HSCT ( n = 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, P = 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%, P = 0.15). The 3-year relapse rates (33% vs 27%, P = 0.84) and non-relapse mortality (21% vs 22%, P = 0.78) did not differ between these two groups. There were also no differences in 3-year overall survival (OS) (48% vs 50%, P = 0.78) and progression-free survival (47% vs 51%, P = 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; P = 0.003) and disease status (stable or progression disease before HSCT: HR, 2.8; P = 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.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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