Indications for allogeneic stem cell transplantation in chronic lymphocytic leukemia: the EBMT transplant consensus

被引:275
作者
Dreger, P.
Corradini, P.
Kimby, E.
Michallet, M.
Milligan, D.
Schetelig, J.
Wiktor-Jedrzejczak, W.
Niederwieser, D.
Hallek, M.
Montserrat, E.
机构
[1] Heidelberg Univ, Dept Med 5, D-69120 Heidelberg, Germany
[2] Univ Milan, Ist Nazl Tumori, Dept Hematol, Milan, Italy
[3] Karolinska Univ Hosp, Hematol Ctr, Huddinge, Sweden
[4] Hop Edouard Herriot, Unite Greffe Cellules Souches Hematopoiet, Lyon, France
[5] Birmingham Heartlands Hosp, Dept Haematol, Birmingham B9 5ST, W Midlands, England
[6] Univ Dresden, Dept Med 1, Dresden, Germany
[7] Med Univ Warsaw, Dept Haematol Oncol & Internal Med, Warsaw, Poland
[8] Univ Leipzig, Dept Hematol & Med Oncol, D-7010 Leipzig, Germany
[9] Univ Cologne, Dept Med 1, Cologne, Germany
[10] Univ Barcelona, Dept Hematol, Inst Hematol & Oncol, Hosp Clin,IDIBAPS, Barcelona, Spain
关键词
CLL; salvage treatment; allogeneic stem cell transplantation; practice guidelines;
D O I
10.1038/sj.leu.2404441
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this project was to identify situations where allogeneic stem cell transplantation (allo-SCT) might be considered as a preferred treatment option for patients with B-cell chronic lymphocytic leukemia (CLL). Based on a MEDLINE search and additional sources, a consented proposal was drafted, refined and approved upon final discussion by an international expert panel. Key elements of the consensus are (1) allo-SCT is a procedure with evidence-based efficacy in poor-risk CLL; (2) although definition of 'poor-risk CLL' requires further investigation, allo-SCT is a reasonable treatment option for younger patients with (i) non-response or early relapse (within 12 months) after purine analogues, (ii) relapse within 24 months after having achieved a response with purine-analogue-based combination therapy or autologous transplantation, and (iii) patients with p53 abnormalities requiring treatment; and (3) optimum transplant strategies may vary according to distinct clinical situations and should be defined in prospective trials. This is the first attempt to define standard indications for allo-SCT in CLL. Nevertheless, whenever possible, allo-SCT should be performed within disease-specific prospective clinical protocols in order to continuously refine transplant indications according to new developments in risk assessment and treatment of CLL.
引用
收藏
页码:12 / 17
页数:6
相关论文
共 43 条
[1]   Perspectives on the use of new diagnostic tools in the treatment of chronic lymphocytic leukemia [J].
Binet, JL ;
Caligaris-Cappio, F ;
Catovsky, D ;
Cheson, B ;
Davis, T ;
Dighiero, G ;
Döhner, H ;
Hallek, M ;
Hillmen, P ;
Keating, M ;
Montserrat, E ;
Kipps, TJ ;
Rai, K .
BLOOD, 2006, 107 (03) :859-861
[2]   Fludarabine, cyclophosphamide and mitoxantrone in the treatment of resistant or relapsed chronic lymphocytic leukaemia [J].
Bosch, F ;
Ferrer, A ;
López-Guillermo, A ;
Giné, E ;
Bellosillo, B ;
Villamor, N ;
Colomer, D ;
Cobo, F ;
Perales, M ;
Esteve, J ;
Altés, A ;
Besalduch, J ;
Ribera, JM ;
Montserrat, E .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (04) :976-984
[3]   Select high-risk genetic features predict earlier progression following chemoimmunotherapy with fludarabine and rituximab in chronic lymphocytic leukemia: Justification for risk-adapted therapy [J].
Byrd, JC ;
Gribben, JG ;
Peterson, BL ;
Grever, MR ;
Lozanski, G ;
Lucas, DM ;
Lampson, B ;
Larson, RA ;
Caligiuri, MA ;
Heerema, NA .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (03) :437-443
[4]  
Byrd John C, 2004, Hematology Am Soc Hematol Educ Program, P163
[5]   Allogeneic transplant with reduced intensity conditioning regimens may overcome the poor prognosis of B-cell chronic lymphocytic leukemia with unmutated immunoglobulin variable heavy-chain gene and chromosomal abnormalities (11q- and 17p-) [J].
Caballero, D ;
García-Macro, JA ;
Martino, R ;
Mateos, V ;
Ribera, JM ;
Sarrá, J ;
León, A ;
Sanz, G ;
la Serna, JC ;
Cabrera, R ;
González, M ;
Sierra, J ;
San Miguel, J .
CLINICAL CANCER RESEARCH, 2005, 11 (21) :7757-7763
[6]   ZAP-70 expression as a surrogate for immunoglobulin-variable-region mutations in chronic lymphocytic leukemia [J].
Crespo, M ;
Bosch, F ;
Villamor, N ;
Bellosillo, B ;
Colomer, D ;
Rozman, M ;
Marcé, S ;
López-Guillermo, A ;
Campo, E ;
Montserrat, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (18) :1764-1775
[7]   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
[8]   In-tandem insight from basic science combined with clinical research: CD38 as both marker and key component of the pathogenetic network underlying chronic lymphocytic leukemia [J].
Deaglio, Silvia ;
Vaisitti, Tiziana ;
Aydin, Semra ;
Ferrero, Enza ;
Malavasi, Fabio .
BLOOD, 2006, 108 (04) :1135-1144
[9]   High remission rate in T-cell prolymphocytic leukemia with CAMPATH-1H [J].
Dearden, CE ;
Matutes, E ;
Cazin, B ;
Tjonnfjord, GE ;
Parreira, A ;
Nomdedeu, B ;
Leoni, P ;
Clark, FJ ;
Radia, D ;
Rassam, SMB ;
Roques, T ;
Ketterer, N ;
Brito-Babapulle, V ;
Dyer, MJS ;
Catovsky, D .
BLOOD, 2001, 98 (06) :1721-1726
[10]   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