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

被引:20
|
作者
Dreger, Peter [1 ]
Doehner, Hartmut [2 ]
McClanahan, Fabienne [1 ]
Busch, Raymonde [3 ]
Ritgen, Matthias [4 ]
Greinix, Hildegard [5 ]
Fink, Anna-Maria [6 ]
Knauf, Wolfgang
Stadler, Michael [7 ]
Pfreundschuh, Michael [8 ]
Duehrsen, Ulrich [9 ]
Brittinger, Guenter [9 ]
Hensel, Manfred [1 ]
Schetelig, Johannes [10 ]
Winkler, Dirk [2 ]
Buehler, Andreas [2 ]
Kneba, Michael [4 ]
Schmitz, Norbert [11 ]
Hallek, Michael [6 ]
Stilgenbauer, Stephan [2 ]
机构
[1] Univ Heidelberg, Dept Med 5, D-69120 Heidelberg, Germany
[2] Univ Ulm, Dept Med 3, Ulm, Germany
[3] Tech Univ Munich, Inst Med Stat & Epidemiol, Munich, Germany
[4] Univ Kiel, Dept Med 2, Kiel, Germany
[5] Med Univ, Dept Internal Med 1, Vienna, Austria
[6] Univ Cologne, Ctr Integrated Oncol Cologne Bonn, Dept Med 1, D-50931 Cologne, Germany
[7] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, D-3000 Hannover, Germany
[8] Univ Saarland, Dept Med 1, D-6650 Homburg, Germany
[9] Univ Essen Gesamthsch, Dept Hematol, Essen, Germany
[10] Univ Hosp Carl Gustav Carus, Dept Med 1, Dresden, Germany
[11] Asklepios Klin St Georg, Dept Hematol Oncol & Stem Cell Transplant, Hamburg, Germany
关键词
BONE-MARROW-TRANSPLANTATION; GENOMIC ABERRATIONS; INITIAL THERAPY; CYCLOPHOSPHAMIDE; FLUDARABINE; RITUXIMAB; RISK; MOBILIZATION; SURVIVAL; REGIMEN;
D O I
10.1182/blood-2011-09-378505
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (Blood. 2012;119(21):4851-4859)
引用
收藏
页码:4851 / 4859
页数:9
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