Autologous peripheral blood stem cell transplantation for acute myeloid leukemia

Author:

Vellenga Edo1,van Putten Wim2,Ossenkoppele Gert J.3,Verdonck Leo F.4,Theobald Matthias5,Cornelissen Jan J.6,Huijgens Peter C.3,Maertens Johan7,Gratwohl Alois8,Schaafsma Ron9,Schanz Urs10,Graux Carlos11,Schouten Harry C.12,Ferrant Augustin13,Bargetzi Mario14,Fey Martin F.15,Löwenberg Bob6,

Affiliation:

1. Department of Hematology, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands;

2. Hovon Data Center and Department of Trials and Statistics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands;

3. Department of Hematology, VU University Medical Center Amsterdam, Amsterdam, The Netherlands;

4. University Medical Center Utrecht, Utrecht, The Netherlands;

5. Department of Internal Medicine III, University Hospital Mainz, Mainz, Germany;

6. Department of Hematology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands;

7. University Hospital Gasthuisberg, Leuven, Belgium;

8. University Hospital Basel, Basel, Switzerland;

9. Medisch Spectrum Twente, Enschede, The Netherlands;

10. Division of Hematology, University Hospital Zürich, Zürich, Switzerland;

11. UCL, MT-Godinne, Yvoir, Belgium;

12. University Medical Center Maastricht, Maastricht, The Netherlands;

13. Hospital St Luc, Bruxelles, Belgium;

14. Center of Hematology/Oncology and Transfusion Medicine Kantonsspittal Aarau, Switzerland; and

15. Department of Medical Oncology, University and Inselspital, Berne, Switzerland

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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