Allogeneic peripheral blood stem cell transplantation using a fludarabine-based low intensity conditioning regimen for malignant lymphoma

被引:143
作者
Nagler, A
Slavin, S
Varadi, G
Naparstek, E
Samuel, S
Or, R
机构
[1] Hadassah Univ Hosp, Dept Bone Marrow Transplant, IL-91120 Jerusalem, Israel
[2] Hadassah Univ Hosp, Canc Immunotherapy & Immunobiol Res Ctr, IL-91120 Jerusalem, Israel
关键词
allogeneic; peripheral blood stem cell transplantation; malignant lymphoma; fludarabine; low intensity conditioning regimen;
D O I
10.1038/sj.bmt.1702392
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Relapse is a serious complication following high-dose therapy and autologous bone marrow transplantation (ABMT) for malignant lymphoma (ML), Allogeneic transplantation (alloSCT) is a therapeutic option. However, it is associated with a high incidence of transplant-related organ toxicity and mortality. We recently reported fast engraftment and minimal transplant-related toxicity, using fludarabine-based conditioning with reduced amounts of chemotoxic drugs prior to alloSCT, We now present our experience with 23 heavily treated high risk ML patients who underwent matched alloSCT following the same low intensity conditioning. The patients (20 male, three female) were aged 13-63 years, Nineteen had NHL and four HD (resistant disease 12, partial remission 11), Five were post ABMT, Twenty-two patients had fully matched sibling donors, and one a fully matched unrelated donor. Engraftment was fast. There was no rejection or non-engraftment, Organ toxicity was moderate with no liver or renal toxicity >grade II, Four patients developed >grade II graft-versus-host disease (GVHD). Seven patients died - four of grade III-IV GVHD and severe infections, two of bacterial sepsis, one of pulmonary failure. Ten patients are alive after 22.5 (15-37) months, Survival and disease-free survival at 37 months are both 40%, Probability of relapse is 26%, These encouraging results suggest that alloSCT following fludarabine-based low intensity conditioning in high-risk patients merits further evaluation.
引用
收藏
页码:1021 / 1028
页数:8
相关论文
共 60 条
[41]  
REECE DE, 1994, BLOOD, V83, P1193
[42]  
ROBERTSON LE, 1993, BLOOD, V81, P143
[43]  
SHIPP MA, 1994, BLOOD, V83, P1165
[44]  
SLAVIN S, 1981, CANCER IMMUNOL IMMUN, V11, P155
[45]  
SLAVIN S, 1991, Current Opinion in Oncology, V3, P254, DOI 10.1097/00001622-199104000-00005
[46]   Nonmyeloablative stem cell transplantation and cell therapy as an alternative to conventional bone marrow transplantation with lethal cytoreduction for the treatment of malignant and nonmalignant hematologic diseases [J].
Slavin, S ;
Nagler, A ;
Naparstek, E ;
Kapelushnik, Y ;
Aker, M ;
Cividalli, G ;
Varadi, G ;
Kirschbaum, M ;
Ackerstein, A ;
Samuel, S ;
Amar, A ;
Brautbar, C ;
Ben-Tal, O ;
Eldor, A ;
Or, R .
BLOOD, 1998, 91 (03) :756-763
[47]   Allogeneic cell therapy with donor peripheral blood cells and recombinant human interleukin-2 to treat leukemia relapse after allogeneic bone marrow transplantation [J].
Slavin, S ;
Naparstek, E ;
Nagler, A ;
Ackerstein, A ;
Samuel, S ;
Kapelushnik, J ;
Brautbar, C ;
Or, R .
BLOOD, 1996, 87 (06) :2195-2204
[48]   Immunotherapy in conjunction with autologous and allogeneic blood or marrow transplantation in lymphoma [J].
Slavin, S ;
Nagler, A .
ANNALS OF ONCOLOGY, 1998, 9 :31-39
[49]   Randomized trial showing equivalent efficacy of filgrastim 5 mu g/kg/d and 10 mu g/kg/d following high-dose chemotherapy and autologous bone marrow transplantation in high-risk lymphomas [J].
Stahel, RA ;
Jost, LM ;
Honegger, H ;
Betts, E ;
Goebel, MEM ;
Nagler, A .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (05) :1730-1735
[50]   HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOR MALIGNANT-LYMPHOMAS [J].
STAHEL, RA ;
JOST, LM ;
PICHERT, G ;
WIDMER, L .
CANCER TREATMENT REVIEWS, 1995, 21 (01) :3-32