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Allogeneic stem cell transplantation provides durable disease control in poor-risk chronic lymphocytic leukemia: long-term clinical and MRD results of the German CLL Study Group CLL3X trial
被引:228
作者:
Dreger, Peter
[1
]
Doehner, Hartmut
[2
]
Ritgen, Matthias
[3
]
Boettcher, Sebastian
[3
]
Busch, Raymonde
[4
]
Dietrich, Sascha
[1
]
Bunjes, Donald
[2
]
Cohen, Sandra
[5
]
Schubert, Joerg
[6
]
Hegenbart, Ute
[1
]
Beelen, Dietrich
[7
]
Zeis, Matthias
[8
]
Stadler, Michael
[9
]
Hasenkamp, Justin
[10
]
Uharek, Lutz
[11
]
Scheid, Christof
[12
]
Humpe, Andreas
[3
]
Zenz, Thorsten
[2
]
Winkler, Dirk
[2
]
Hallek, Michael
[12
]
Kneba, Michael
[3
]
Schmitz, Norbert
[8
]
Stilgenbauer, Stephan
[2
]
机构:
[1] Univ Heidelberg, Dept Med V, D-69120 Heidelberg, Germany
[2] Univ Ulm, Dept Med 3, Ulm, Germany
[3] Univ Schleswig Holstein, Dept Med 2, Kiel, Germany
[4] Tech Univ Munich, Inst Med Stat & Epidemiol, Munich, Germany
[5] Hop Maison Neuve Rosemont, Montreal, PQ H1T 2M4, Canada
[6] Univ Saarland, Dept Med 1, D-6650 Homburg, Germany
[7] Univ Essen Gesamthsch, Dept Bone Marrow Transplant, Essen, Germany
[8] Asklepios Klin St Georg, Dept Hematol & Stem Cell Transplantat, Hamburg, Germany
[9] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, D-3000 Hannover, Germany
[10] Univ Gottingen, Dept Hematol & Oncol, Gottingen, Germany
[11] Univ Med Berlin, Dept Med 3, Charite Campus Benjamin Franklin, Berlin, Germany
[12] Univ Cologne, Dept Med 1, Ctr Integrated Oncol Cologne Bonn, Cologne, Germany
来源:
关键词:
GRAFT-VERSUS-LEUKEMIA;
TREATMENT-RELATED MORTALITY;
MINIMAL RESIDUAL DISEASE;
GENE MUTATION STATUS;
HEAVY-CHAIN GENE;
MARROW-TRANSPLANTATION;
CD38;
EXPRESSION;
GENOMIC ABERRATIONS;
FLUDARABINE;
SURVIVAL;
D O I:
10.1182/blood-2010-03-275420
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The purpose of this prospective multicenter phase 2 trial was to investigate the long-term outcome of reduced-intensity conditioning allogeneic stem cell transplantation (alloSCT) in patients with poor-risk chronic lymphocytic leukemia. Conditioning was fludarabine/cyclophosphamide-based. Longitudinal quantitative monitoring of minimal residual disease (MRD) was performed centrally by MRD-flow or real-time quantitative polymerase chain reaction. One hundred eligible patients were enrolled, and 90 patients proceeded to alloSCT. With a median follow-up of 46 months (7-102 months), 4-year nonrelapse mortality, event-free survival (EFS) and overall survival (OS) were 23%, 42%, and 65%, respectively. Of 52 patients with MRD monitoring available, 27 (52%) were alive and MRD negative at 12 months after transplant. Four-year EFS of this subset was 89% with all event-free patients except for 2 being MRD negative at the most recent assessment. EFS was similar for all genetic subsets, including 17p deletion (17p-). In multivariate analyses, uncontrolled disease at alloSCT and in vivo T-cell depletion with alemtuzumab, but not 17p-, previous purine analogue refractoriness, or donor source (human leukocyte antigen-identical siblings or unrelated donors) had an adverse impact on EFS and OS. In conclusion, alloSCT for poor-risk chronic lymphocytic leukemia can result in long-term MRD-negative survival in up to one-half of the patients independent of the underlying genomic risk profile. This trial is registered at http://clinicaltrials.gov as NCT00281983. (Blood. 2010;116(14):2438-2447)
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页码:2438 / 2447
页数:10
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