Autologous bone marrow transplantation for high risk acute lymphoblastic leukemia:: clinical relevance of ex vivo bone marrow purging with monoclonal antibodies and complement

被引:21
作者
Grañena, A
Castellsagué, X
Badell, I
Ferra, C
Ortega, JJ
Brunet, S
Puntí, C
Sureda, A
Picón, M
Valls, A
Rutllant, ML
García, J
机构
[1] Hosp Duran & Reynals, Inst Catala Oncol, Dept Hematol, Barcelona 08907, Spain
[2] Hosp Duran & Reynals, Inst Catala Oncol, Dept Canc Epidemiol, Barcelona, Spain
[3] Hosp Santa Creu & Sant Pau, Dept Pediat, Barcelona, Spain
[4] Hosp Gen Valle Hebron, Dept Pediat, Barcelona, Spain
[5] Hosp Santa Creu & Sant Pau, Dept Hematol, Barcelona, Spain
[6] Hosp Duran & Reynals, Inst Recerca Oncol, Cryobiol & Cell Therapy Dept, Barcelona, Spain
[7] Hosp Esperanza, Dept Radiotherapy, Barcelona, Spain
关键词
autologous BMT; acute lymphocytic leukemia; bone marrow purging;
D O I
10.1038/sj.bmt.1701957
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Herein we describe our experience with 75 consecutive autologous BM transplants for patients with high-risk ALL, with special attention to the clinical impact of BM purging. Fifty-two patients received purged BM using monoclonal antibody (MoAb) cocktails and complement, and 23 patients received untreated BM. The distribution of prognostic factors was similar in both groups. Hemopoietic reconstitution was adequate and did not differ in the two groups. Transplant-related mortality was 9.6% and 13% in 'purged' and 'unpurged' groups. Median follow up was 11 months (2-71) and overall actuarial probability of disease-free survival (DFS) at 5 years was 40% (53% relapse probability). We found a beneficial effect of purging in patients over 15 years of age and in patients needing more than 1 month to reach CR1, Patients in CRI receiving purged marrow had a longer DFS and a lower relapse probability (52% vs 12%, P=0.02 and 35% vs 86%, P = 0.005, respectively) which were related to the efficacy of the purging procedure (more or less than one log of depletion). In further CR, no advantage of purging has been found. Our data strongly suggest the clinical relevance of BM purging in autologous BMT in high-risk ALL patients and support the need for prospective randomized studies.
引用
收藏
页码:621 / 627
页数:7
相关论文
共 53 条
[1]   PROSPECTIVE GENETICALLY RANDOMIZED COMPARISON BETWEEN INTENSIVE POSTINDUCTION CHEMOTHERAPY AND BONE-MARROW TRANSPLANTATION IN ADULTS WITH NEWLY-DIAGNOSED ACUTE MYELOID-LEUKEMIA [J].
ARCHIMBAUD, E ;
THOMAS, X ;
MICHALLET, M ;
JAUBERT, J ;
TRONCY, J ;
GUYOTAT, D ;
FIERE, D .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (02) :262-267
[2]  
BALL ED, 1990, BLOOD, V75, P1199
[3]  
BEAUJEAN F, 1995, BONE MARROW TRANSPL, V15, P691
[4]  
BEELEN DW, 1989, BLOOD, V74, P1507
[5]   GENE-MARKING TO TRACE ORIGIN OF RELAPSE AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION [J].
BRENNER, MK ;
RILL, DR ;
MOEN, RC ;
KRANCE, RA ;
MIRRO, J ;
ANDERSON, WF ;
IHLE, JN .
LANCET, 1993, 341 (8837) :85-86
[6]  
BUCKNER CD, 1983, RECENT ADV BONE MARR, P599
[7]  
CARELLA AM, 1988, BONE MARROW TRANSPL, V3, P537
[8]   AUTOLOGOUS BONE-MARROW TRANSPLANT IN ACUTE MYELOID-LEUKEMIA IN 1ST REMISSION [J].
CASSILETH, PA ;
ANDERSEN, J ;
LAZARUS, HM ;
COLVIN, OM ;
BENNETT, JM ;
STADTMAUER, EA ;
KAIZER, H ;
WEINER, RS ;
EDELSTEIN, M ;
OKEN, MM .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (02) :314-319
[9]  
CHAMPLIN R, 1987, SEMIN HEMATOL, V24, P55
[10]  
CHAMPLIN R, 1994, BONE MARROW TRANSPL, P595