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Role of upfront autologous transplant for peripheral T-cell lymphoma patients achieving a complete remission with first-line therapy: a systematic review and meta-analysis.
Girard, L; Koh, Y J; Koh, L P; Chee, Y L; Chan, H L; Lee, J; de Mel, S; Poon, L M; Samuel, M.
Afiliação
  • Girard L; Aberdeen Royal Infirmary, National Health Service Grampian, Aberdeen, UK.
  • Koh YJ; University College London Medical School, London, UK.
  • Koh LP; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore.
  • Chee YL; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore.
  • Chan HL; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore.
  • Lee J; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore.
  • de Mel S; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore.
  • Poon LM; Department of Haematology Oncology, National University Cancer Institute, Singapore, Singapore. Michelle_Poon@nuhs.edu.sg.
  • Samuel M; NUS Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Bone Marrow Transplant ; 59(6): 838-848, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38443704
ABSTRACT
There is currently no consensus on the role of upfront autologous transplantation (ASCT) for patients with peripheral T-cell lymphomas (PTCL), especially in patients achieving first complete remission (CR1) following chemotherapy, and data in the literature is conflicting. A systematic review and meta-analysis was performed to address this question. We searched key databases from January 2000 to February 2022. Six prospective and eleven retrospective studies were included among 2959 unique records. Median follow up in these studies ranged from 22 to 94 months. There was a trend towards benefit in PFS (HR = 0.80, 95% CI 0.62-1.05, p = 0.11) and OS (HR = 0.79, 95% CI 0.57-1.09, p = 0.15) in the ASCT compared to chemotherapy only group. Importantly, in transplant eligible patients in CR1, a significant benefit was demonstrated in both OS (HR = 0.59, 95% CI 0.36-0.95, p = 0.03) and PFS (HR = 0.61, 95% CI 0.47-0.81, p = 0.0004) in the ASCT group. Amongst the nodal PTCL subgroups, ASCT showed a significant PFS benefit for the AITL subgroup (HR = 0.43, 95% CI 0.20-0.94, p < 0.03) but not PTCL-NOS or ALK-ve ALCL subgroups. Our findings support upfront ASCT for transplant eligible PTCL patients achieving CR1 post chemotherapy. In particular, patients with AITL exhibited a significantly better PFS after upfront ASCT.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Autólogo / Indução de Remissão / Linfoma de Células T Periférico Limite: Humans Idioma: En Revista: Bone Marrow Transplant Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Autólogo / Indução de Remissão / Linfoma de Células T Periférico Limite: Humans Idioma: En Revista: Bone Marrow Transplant Ano de publicação: 2024 Tipo de documento: Article