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In search of the optimal platform for Post-Allogeneic SCT immunotherapy in relapsed multiple myeloma: a systematic review.
Oostvogels, R; Uniken Venema, S M; de Witte, M; Raymakers, R; Kuball, J; Kröger, N; Minnema, M C.
Afiliação
  • Oostvogels R; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
  • Uniken Venema SM; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
  • de Witte M; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
  • Raymakers R; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
  • Kuball J; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
  • Kröger N; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Minnema MC; Department of Hematology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
Bone Marrow Transplant ; 52(9): 1233-1240, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28692028
ABSTRACT
Allogeneic stem cell transplantation (allo-SCT) has the potential to induce sustained remissions in patients with multiple myeloma (MM). Currently, allo-SCT is primarily performed in high-risk MM patients, most often in the setting of early relapse after first-line therapy with autologous SCT. However, the implementation of allo-SCT for MM is jeopardized by high treatment-related mortality (TRM) rates as well as high relapse rates. In this systematic review, we aimed to identify a safe allo-SCT strategy that has optimal 1-year results regarding mortality, relapse and severe GvHD, creating opportunities for post-transplantation strategies to maintain remissions in the high-risk group of relapsed MM patients. Eleven studies were included. Median PFS ranged from 5.2 to 36.8 months and OS was 13.0 to 63.0 months. The relapse related mortality at 1 year varied between 0 and 50% and TRM between 8 and 40%. Lowest GvHD incidences were reported for conditioning regimens with T-cell depletion using ATG or graft CD34+ selection. Similar strategies could lay the foundation for a post-transplant immune platform, this should be further evaluated in prospective clinical trials.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Homólogo / Transplante de Células-Tronco Hematopoéticas / Condicionamento Pré-Transplante / Imunoterapia / Mieloma Múltiplo Tipo de estudo: Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante Homólogo / Transplante de Células-Tronco Hematopoéticas / Condicionamento Pré-Transplante / Imunoterapia / Mieloma Múltiplo Tipo de estudo: Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda