Results of alemtuzumab-based reduced-intensity allogeneic transplantation for chronic lymphocytic leukemia: a British Society of Blood and Marrow Transplantation Study

被引:119
作者
Delgado, J
Thomson, K
Russell, N
Ewing, J
Stewart, W
Cook, G
Devereux, S
Lovell, R
Chopra, R
Marks, DI
Mackinnon, S
Milligan, DW [1 ]
机构
[1] Birmingham Heartlands Hosp, Dept Hematol, Birmingham B9 5SS, W Midlands, England
[2] Royal Free Hosp, London NW3 2QG, England
[3] UCL Hosp, London, England
[4] City Hosp Nottingham, Nottingham, England
[5] St James Univ Hosp, Leeds, W Yorkshire, England
[6] Kings Coll Hosp London, London, England
[7] Christie Hosp, Manchester, Lancs, England
[8] Bristol Royal Childrens Hosp, Bristol, Avon, England
关键词
D O I
10.1182/blood-2005-08-3372
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report results in 41 consecutive patients with chronic lymphocytic leukemia (CLL) who underwent allogeneic hematopoietic cell transplantation (HCT) after fludarabine, melphalan, and alemtuzumab conditioning. Donors were 24 HLA-matched siblings and 17 unrelated volunteers, 4 of them mismatched with recipients. All but 3 patients had initial hematologic recovery, but 5 more patients had secondary graft failure. Median intervals to neutrophil (greater than 0.5 x 10(9)/L) and platelet (greater than 20 x 10(9)/L) recovery were 14 days (range, 9-30 days) and 11 days (range, 8-45 days), respectively. Eleven (27%) patients had relapses and received escalated donor lymphocyte infusions, but only 3 of them had sustained responses. Acute and chronic graft-versus-host disease (GVHD) was observed in 17 (41%) and 13 (33%) patients, respectively. Seventeen (41%) patients have died, 5 of progressive disease. The 2-year overall survival and transplantation-related mortality (TRM) rates were 51% (95% confidence interval [CI], 33%-69%) and 26% (95% CI, 14%-46%), respectively. The alemtuzumab-based regimen was feasible and effective in patients with CLL with a relatively low rate of GVHD. However, TRM remains relatively high as a result of a variety of viral and fungal infections. Studies are ongoing to address the efficacy of reduced doses of alemtuzumab in this group of immunosuppressed patients.
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页码:1724 / 1730
页数:7
相关论文
共 42 条
[1]   Incidence and outcome of Adenovirus disease in transplant recipients after reduced-intensity conditioning with alemtuzumab [J].
Avivi, I ;
Chakrabarti, S ;
Milligan, DW ;
Waldmann, H ;
Hale, G ;
Osman, H ;
Ward, KN ;
Fegan, CD ;
Yong, K ;
Goldstone, AH ;
Limb, DC ;
MacKinnon, S .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2004, 10 (03) :186-194
[2]   Respiratory virus infections in transplant recipients after reduced-intensity conditioning with Campath-1H: high incidence but low mortality [J].
Chakrabarti, S ;
Avivi, I ;
Mackinnon, S ;
Ward, K ;
Kottaridis, PD ;
Osman, H ;
Waldmann, H ;
Hale, G ;
Fegan, CD ;
Yong, K ;
Goldstone, AH ;
Linch, DC ;
Milligan, DW .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (04) :1125-1132
[3]   High incidence of cytomegalovirus infection after nonmyeloablative stem cell transplantation: potential role of Campath-1H in delaying immune reconstitution [J].
Chakrabarti, S ;
Mackinnon, S ;
Chopra, R ;
Kottaridis, PD ;
Peggs, K ;
O'Gorman, P ;
Chakraverty, R ;
Marshall, T ;
Osman, H ;
Mahendra, P ;
Craddock, C ;
Waldmann, H ;
Hale, G ;
Fegan, CD ;
Yong, K ;
Goldstone, AH ;
Linch, DC ;
Milligan, DW .
BLOOD, 2002, 99 (12) :4357-4363
[4]   Limiting transplantation-related mortality following unrelated donor stem cell transplantation by using a nonmyeloablative conditioning regimen [J].
Chakraverty, R ;
Peggs, K ;
Chopra, R ;
Milligan, DW ;
Kottaridis, PD ;
Verfuerth, S ;
Geary, J ;
Thuraisundaram, D ;
Branson, K ;
Chakrabarti, S ;
Mahendra, P ;
Craddock, C ;
Parker, A ;
Hunter, A ;
Hale, G ;
Waldmann, H ;
Williams, CD ;
Yong, K ;
Linch, DC ;
Goldstone, AH ;
Mackinnon, S .
BLOOD, 2002, 99 (03) :1071-1078
[5]   National Cancer Institute-sponsored Working Group guidelines for chronic lymphocytic leukemia: Revised guidelines for diagnosis and treatment [J].
Cheson, BD ;
Bennett, JM ;
Grever, M ;
Kay, N ;
Keating, MJ ;
OBrien, S ;
Rai, KR .
BLOOD, 1996, 87 (12) :4990-4997
[6]  
Curtis RE, 1999, BLOOD, V94, P2208
[7]  
DAY BR, 2005, BRIT J HAEMATOL, V128, P351
[8]   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
[9]   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
[10]   Autologous and allogeneic stem cell transplantation for chronic lymphocytic leukemia [J].
Dreger, P ;
Montserrat, E .
LEUKEMIA, 2002, 16 (06) :985-992