Early autologous stem cell transplantation for chronic lymphocytic leukemia: long-term follow-up of the German CLL Study Group CLL3 trial

Author:

Dreger Peter1,Döhner Hartmut2,McClanahan Fabienne1,Busch Raymonde3,Ritgen Matthias4,Greinix Hildegard5,Fink Anna-Maria6,Knauf Wolfgang7,Stadler Michael8,Pfreundschuh Michael9,Dührsen Ulrich10,Brittinger Günter10,Hensel Manfred1,Schetelig Johannes11,Winkler Dirk2,Bühler Andreas2,Kneba Michael4,Schmitz Norbert12,Hallek Michael6,Stilgenbauer Stephan2

Affiliation:

1. Department of Medicine V, University of Heidelberg, Heidelberg, Germany;

2. Department of Medicine III, University of Ulm, Ulm, Germany;

3. Institute of Medical Statistics and Epidemiology, Technical University Munich, Munich, Germany;

4. Department of Medicine II, University of Schleswig-Holstein, Kiel, Germany;

5. Department of Internal Medicine I, Medical University, Vienna, Austria;

6. Department of Medicine I, Center for Integrated Oncology Cologne Bonn, University of Cologne, Cologne, Germany;

7. Oncology Care, Im Prüfling, Frankfurt, Germany;

8. Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany;

9. Department of Medicine I, University of Saarland, Homburg, Germany;

10. Department of Hematology, University of Essen, Essen, Germany;

11. Department of Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; and

12. Department of Hematology, Oncology, and Stem Cell Transplantation, Asklepios Klinik St Georg, Hamburg, Germany

Abstract

Abstract The CLL3 trial was designed to study intensive treatment including autologous stem cell transplantation (autoSCT) as part of first-line therapy in patients with chronic lymphocytic leukemia (CLL). Here, we present the long-term outcome of the trial with particular focus on the impact of genomic risk factors, and we provide a retrospective comparison with patients from the fludarabine-cyclophosphamide-rituximab (FCR) arm of the German CLL Study Group (GCLLSG) CLL8 trial. After a median observation time of 8.7 years (0.3-12.3 years), median progression-free survival (PFS), time to retreatment, and overall survival (OS) of 169 evaluable patients, including 38 patients who did not proceed to autoSCT, was 5.7, 7.3, and 11.3 years, respectively. PFS and OS were significantly reduced in the presence of 17p- and of an unfavorable immunoglobulin heavy variable chain mutational status, but not of 11q-. Five-year nonrelapse mortality was 6.5%. When 110 CLL3 patients were compared with 126 matched patients from the FCR arm of the CLL8 trial, 4-year time to retreatment (75% vs 77%) and OS (86% vs 90%) was similar despite a significant benefit for autoSCT in terms of PFS. In summary, early treatment intensification including autoSCT can provide very effective disease control in poor-risk CLL, although its clinical benefit in the FCR era remains uncertain. The trial has been registered with www.clinicaltrials.gov as NCT00275015.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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