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CD34+ selected versus unselected autologous stem cell transplantation in patients with advanced-stage mantle cell and diffuse large B-cell lymphoma.
Berger, Martin D; Branger, Giacomo; Leibundgut, Kurt; Baerlocher, Gabriela M; Seipel, Katja; Mueller, Beatrice U; Gregor, Michael; Ruefer, Axel; Pabst, Thomas.
Afiliação
  • Berger MD; Department of Medical Oncology, University Hospital and University of Berne, Berne, Switzerland.
  • Branger G; Department of Medical Oncology, University Hospital and University of Berne, Berne, Switzerland.
  • Leibundgut K; Department of Pediatrics, University Hospital and University of Berne, Berne, Switzerland.
  • Baerlocher GM; Department of Hematology, University Hospital and University of Berne, Berne, Switzerland.
  • Seipel K; Department of Clinical Research, University Hospital and University of Berne, Berne, Switzerland.
  • Mueller BU; Department of Clinical Research, University Hospital and University of Berne, Berne, Switzerland.
  • Gregor M; Department of Hematology, Kantonsspital, Lucerne, Switzerland.
  • Ruefer A; Department of Hematology, Kantonsspital, Lucerne, Switzerland.
  • Pabst T; Department of Medical Oncology, University Hospital and University of Berne, Berne, Switzerland; Department of Clinical Research, University Hospital and University of Berne, Berne, Switzerland. Electronic address: thomas.pabst@insel.ch.
Leuk Res ; 39(6): 561-7, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25890431
ABSTRACT
Novel strategies aiming to increase survival rates in patients with advanced-stage mantle cell lymphoma (MCL) and relapsing diffuse large B-cell lymphoma (DLBCL) are a clinical need. High-dose chemotherapy (HDCT) with autologous stem cell transplantation (ASCT) has improved progression-free (PFS) and overall survival (OS) in MCL and relapsed DLBCL. However, the role of CD34+ cell selection before ASCT in MCL and DLBCL is unclear. We retrospectively analyzed the outcome of 62 consecutive patients with advanced-stage MCL or relapsed DLBCL undergoing ASCT with (n=31) or without (n=31) prior CD34+ selection. All patients had stage III or IV disease, with 47% having DLBCL and 53% MCL. The median duration for neutrophil and platelet recovery was 12 and 16 days in CD34+ selected patients, and 11 (P<.001) and 14 days (P=.012) in the group without selection, respectively. No differences in toxicities were observed. The 5-year PFS for CD34+ selected versus not selected patients was 67% and 39% (P=.016), and the 5-year OS was 86% and 54% (P=.007). Our data suggest that using CD34+ selected autografts for ASCT in advanced stage MCL and DLBCL is associated with longer PFS and OS without increased toxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article