Autologous peripheral blood stem cell transplantation for acute myeloid leukemia

  • E Vellenga
  • , W van Putten
  • , GJ Ossenkoppele
  • , LF Verdonck
  • , M Theobald
  • , Jan Cornelissen
  • , PC Huijgens
  • , J Maertens
  • , A Gratwohl
  • , R Schaafsma
  • , U Schanz
  • , C Graux
  • , HC (Harry) Schouten
  • , A Ferrant
  • , M Bargetzi
  • , MF Fey
  • , Bob Löwenberg

Research output: Contribution to journalArticleAcademicpeer-review

110 Citations (Scopus)

Abstract

We report the results of a prospective, randomized phase 3 trial evaluating autologous peripheral blood stem cell transplantation (ASCT) versus intensive consolidation chemotherapy in newly diagnosed AML patients in complete remission (CR1). Patients with AML (16-60 years) in CR1 after 2 cycles of intensive chemotherapy and not eligible for allogeneic SCT were randomized between intensive chemotherapy with etoposide and mitoxantrone or ASCT ater high-dose cyclophosphamide and busulfan. Of patients randomized (chemotherapy, n = 259; ASCT, n = 258), more than 90% received their assigned treatment. The 2 groups were comparable with regard to prognostic factors. The ASCT group showed a markedly reduced relapse rate (58% vs 70%, P = .02) and better relapse-free survival at 5 years (38% vs 29%, P = .065, hazard ratio = 0.82; 95% confidence interval, 0.66-1.1) with nonrelapse mortality of 4% versus 1% in the chemotherapy arm (P = .02). Overall survival was similar (44% vs 41% at 5 years, P = .86) because of more opportunities for salvage with second-line chemotherapy and stem cell transplantation in patients relapsing on the chemotherapy arm. This large study shows a relapse advantage for ASCT as postremission therapy but similar survival because more relapsing patients on the chemotherapy arm were salvaged with a late transplantation for relapse. This trial is registered at www.trialregister.nl as # NTR230 and #NTR291. (Blood. 2011;118(23):6037-6042)
Original languageUndefined/Unknown
Pages (from-to)6037-6042
Number of pages6
JournalBlood
Volume118
Issue number23
DOIs
Publication statusPublished - 2011

Research programs

  • EMC MM-02-41-03

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