Abstract

Hematopoietic stem cell transplant (HSCT) is an advisable option for refractory or relapsed peripheral T-cell lymphoma (R/R-PTCL), but whether allogeneic HSCT or autologous HSCT is more beneficial is unknown. To compare the effectiveness and safety of allogeneic HSCT vs autologous HSCT in patients with R/R-PTCL. A systematic search of the PubMed, Embase, the Cochrane Central Register of Controlled Trials, Wanfang, and China National Knowledge Infrastructure databases with the search items refractory or relapsed peripheral T-cell lymphoma, ASCT/autologous stem-cell transplantation, allo-HSCT/allogeneic stem-cell transplantation, therapeutic effect, and treatment was conducted for articles published from January 12, 2001, to October 1, 2020. After duplicate and irrelevant publications were discarded, 329 were ineligible according to the inclusion (clinical trials or retrospective studies with >10 samples) and exclusion criteria (articles without overall survival [OS], progression-free survival [PFS], and transplantation-related mortality [TRM]). Thirty trials were included in the meta-analysis. The study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. Data on study design, individual characteristics, and outcomes were extracted. All statistics were pooled by applying a random-effects model. The prespecified main outcomes were OS, PFS, and TRM. Of 6548 articles, data extracted from the 30 studies (including 880 patients who underwent allogeneic HSCT and 885 who underwent autologous HSCT) were included in this meta-analysis. In the allogeneic HSCT group, a 3-year OS of 50% (95% CI, 41%-60%) and PFS of 42% (95% CI, 35%-51%), a 5-year OS of 54% (95% CI, 47%-62%) and PFS of 48% (95% CI, 40%-56%), and a 3-year TRM of 32% (95% CI, 27%-37%) were observed. In the autologous HSCT group, a 3-year OS of 55% (95% CI, 48%-64%) and PFS of 41% (95% CI, 33%-51%), a 5-year OS of 53% (95% CI, 44%-64%) and PFS of 40% (95% CI, 24%-58%), and a 3-year TRM of 7% (95% CI, 2%-23%) were observed. In this systematic review and meta-analysis, OS and PFS were similar in the allogeneic HSCT and autologous HSCT groups; however, allogeneic HSCT was associated with specific survival benefits among patients with R/R-PTCL.

Highlights

  • Peripheral T-cell lymphomas (PTCLs), a rare and heterogeneous group of non-Hodgkin lymphomas, have a dismal prognosis.[1]

  • In this systematic review and meta-analysis, overall survival (OS) and progression-free survival (PFS) were similar in the allogeneic hematopoietic stem cell transplant (HSCT) and autologous HSCT groups; allogeneic HSCT was associated with specific survival benefits among patients with R/R-PTCL

  • Patients with R/R-PTCL undergoing allogeneic HSCT and autologous HSCT had similar survival conditions, whereas graftvs-host disease (GVHD) and higher transplantation-related mortality (TRM) occurred in the allogeneic HSCT group

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Summary

Introduction

Peripheral T-cell lymphomas (PTCLs), a rare and heterogeneous group of non-Hodgkin lymphomas, have a dismal prognosis.[1]. A study[3] reported poor survival outcomes for 153 patients with refractory or relapsed PTCL (R/R-PTCL) receiving chemotherapy without hematopoietic transplantation, with a median overall survival (OS) of 13.7 months and progression-free survival (PFS) of 5 months. Because of the multitudinous morphologic features of the subtypes and the lack of randomized clinical trials, treatment of this disease remains a challenge, especially for R/R-PTCL.[4]. The concept of high-dose chemotherapy followed by autologous HSCT during first remission in patients with PTCL has been widely accepted by clinical practitioners.[5,6,7] the roles of autologous HSCT and allogeneic HSCT in R/R-PTCL remain far more controversial. This meta-analysis was performed to compare the efficacy and safety of autologous HSCT vs allogeneic HSCT in R/R-PTCL

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