Graft-versus-leukemia activity may overcome therapeutic resistance of chronic lymphocytic leukemia with unmutated immunoglobulin variable heavy-chain gene status:: implications of minimal residual disease measurement with quantitative PCR

被引:131
作者
Ritgen, M
Stilgenbauer, S
von Neuhoff, N
Humpe, A
Brüggemann, M
Pott, C
Raff, T
Kröber, A
Bunjes, D
Schlenk, R
Schmitz, N
Döhner, H
Kneba, M
Dreger, P
机构
[1] Univ Kiel, Dept Internal Med 2, D-24116 Kiel, Germany
[2] Univ Ulm, Dept Internal Med 3, D-89069 Ulm, Germany
[3] Leibniz Univ Hannover, Inst Cellular & Mol Pathol, D-30167 Hannover, Germany
[4] Allgemein Krankenhaus St Georg, Dept Hematol, Hamburg, Germany
关键词
D O I
10.1182/blood-2003-12-4321
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to investigate if graft-versus-leukemia (GVL) activity conferred by allogeneic stem cell transplantation (allo-SCT) is effective in chronic lymphocytic leukemia (CLL) with unmutated V-H gene status. The kinetics of residual disease (MRD) were measured by quantitative allele-specific immunoglobulin heavy chain (IgH) polymerase chain reaction (PCR) in 9 patients after nonmyeloablative allo-SCT for unmutated CLL. Despite an only modest decrease in the early posttransplantation phase, MRD became undetectable in 7 of 9 patients (78%) from day +100 onwards subsequent to chronic graft-versus-host disease or donor lymphocyte infusions. With a median follow-up of 25 months (range, 14-37 months), these 7 patients remain in continuous clinical and molecular remission. In contrast, PCR negativity was achieved in only 6 of 26 control patients (23%) after autologous SCT for unmutated CLL and it was not durable. Taken together, this study shows for the first time that GVL-mediated immunotherapy might be effective in CLL with unmutated V-H.
引用
收藏
页码:2600 / 2602
页数:3
相关论文
共 23 条
[1]   Improved assessment of minimal residual disease in B cell malignancies using fluorogenic consensus probes for real-time quantitative PCR [J].
Brüggemann, M ;
Droese, J ;
Bolz, I ;
Lüth, P ;
Pott, C ;
von Neuhoff, N ;
Scheuering, U ;
Kneba, M .
LEUKEMIA, 2000, 14 (08) :1419-1425
[2]   Ig V gene mutation status and CD38 expression as novel prognostic indicators in chronic lymphocytic leukemia [J].
Damle, RN ;
Wasil, T ;
Fais, F ;
Ghiotto, F ;
Valetto, A ;
Allen, SL ;
Buchbinder, A ;
Budman, D ;
Dittmar, K ;
Kolitz, J ;
Lichtman, SM ;
Schulman, P ;
Vinciguerra, VP ;
Rai, KR ;
Ferrarini, M ;
Chiorazzi, N .
BLOOD, 1999, 94 (06) :1840-1847
[3]   Genomic aberrations and survival in chronic lymphocytic leukemia. [J].
Döhner, H ;
Stilgenbauer, S ;
Benner, A ;
Leupolt, E ;
Kröber, A ;
Bullinger, L ;
Döhner, K ;
Bentz, M ;
Lichter, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (26) :1910-1916
[4]   Allogeneic related donor hematopoietic stem cell transplantation for treatment of chronic lymphocytic leukemia [J].
Doney, KC ;
Chauncey, T ;
Appelbaum, FR .
BONE MARROW TRANSPLANTATION, 2002, 29 (10) :817-823
[5]   The prognostic impact of autologous stem cell transplantation in patients with chronic lymphocytic leukemia:: a risk-matched analysis based on the VH gene mutational status [J].
Dreger, P ;
Stilgenbauer, S ;
Benner, A ;
Ritgen, M ;
Kröber, A ;
Kneba, M ;
Schmitz, N ;
Döhner, H .
BLOOD, 2004, 103 (07) :2850-2858
[6]  
Dreger P, 2003, BONE MARROW TRANSPL, V31, pS56
[7]   Treatment-related mortality and graft-versus-leukemia activity after allogeneic stem cell transplantation for chronic lymphocytic leukemia using intensity-reduced conditioning [J].
Dreger, P ;
Brand, R ;
Hansz, J ;
Milligan, D ;
Corradini, P ;
Finke, J ;
Deliliers, GL ;
Martino, R ;
Russell, N ;
van Biezen, A ;
Michallet, M ;
Niederwieser, D .
LEUKEMIA, 2003, 17 (05) :841-848
[8]  
DREGER P, 2000, BONE MARROW TRANS S1, V25, pS9
[9]  
Esteve J, 2001, BLOOD, V98, p482A
[10]   Unmutated Ig VH genes are associated with a more aggressive form of chronic lymphocytic leukemia [J].
Hamblin, TJ ;
Davis, Z ;
Gardiner, A ;
Oscier, DG ;
Stevenson, FK .
BLOOD, 1999, 94 (06) :1848-1854