| Literature DB >> 30539277 |
Zhenyang Gu1, Lu Wang1,2, Quanshun Wang1, Honghua Li1, Jian Bo1, Shuhong Wang1, Yu Zhao1, Fei Li1, Chunji Gao3,4, Daihong Liu5, Wenrong Huang6,7.
Abstract
There was limited information about the efficacy of myeloablative allogeneic peripheral blood stem cell transplantation (allo-PBSCT) in non-complete remission (non-CR) patients with relapsed/refractory peripheral T cell lymphomas (PTCLs). We conducted a retrospective study of 21 consecutive non-CR patients with relapsed/refractory PTCLs who received myeloablative allo-PBSCT between January 2008 and June 2016. The median follow-up of survivors was 46.5 months (range, 14-105 months). The estimated 3-year relapse rate was 24% (95% CI, 9 to 43%). The 3-year non-relapsed mortality rate was 24% (95% CI, 9 to 44%). Overall, the estimated 3-year overall survival was 47% (95% CI, 25 to 66%). And the estimated 3-year progression-free survival was 46% (95% CI, 24 to 66%). Specifically, eight patients failed to achieve a CR at the first evaluation 3 months after allo-PBSCT and received withdraw of immunosuppression. Five patients also received donor lymphocytes infusions. Five (5/8, 62.5%) patients responded subsequently to these interventions (complete = 4, partial = 1). Overall, ten patients were alive at our last follow-ups, and durable CR were achieved in nine patients without further therapy. Five (50%) of these ten alive patients experienced chronic graft-versus-host disease (GVHD). Our favorable clinical outcomes suggested myeloablative allo-PBSCT was a valid therapeutic option for non-CR patients with relapsed/refractory PTCLs. The sustained CR after immunotherapeutic intervention and high prevalence of chronic GVHD in alive patients provided evidence of graft versus T cell lymphoma effects.Entities:
Keywords: Allogeneic peripheral blood stem cell transplantation; Graft versus lymphoma effects; Non-CR; Peripheral T cell lymphoma; Relapsed/refractory
Mesh:
Year: 2018 PMID: 30539277 DOI: 10.1007/s00277-018-3559-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673