Autologous and allogeneic stem cell transplantations for poor-risk chronic lymphocytic leukemia

被引:160
作者
Gribben, JG
Zahrieh, D
Stephans, K
Bartlett-Pandite, L
Alyea, EP
Fisher, DC
Freedman, AS
Mauch, P
Schlossman, R
Sequist, LV
Soiffer, RJ
Marshall, B
Neuberg, D
Ritz, J
Nadler, LM
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med, Boston, MA USA
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Radiat Oncol, Boston, MA USA
关键词
D O I
10.1182/blood-2005-05-1778
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report here on the long-term follow-up on 162 patients with high-risk chronic lymphocytic leukemia (CLL) who have undergone hematopoietic stem cell transplantation (SCT) at a single center from 1989 to 1999. Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent T-cell-depleted allogeneic SCT, and 137 patients without HLA-matched sibling donors underwent autologous SCT. The 100-day mortality was 4% for both groups, but later morbidity and mortality were negatively affected on outcome. Progression-free survival was significantly longer following autologous than allogeneic SCT, but there was no difference in overall survival and no difference in the cumulative incidence of disease recurrence or deaths without recurrence between the 2 groups. At a median follow-up of 6.5 years there is no evidence of a plateau of progression-free survival. The majority of patients treated with donor lymphocyte infusions after relapse responded, demonstrating a significant graft-versus-leukemia effect in CLL. From these findings we have altered our approach for patients with high-risk CLL and are currently exploring the role of related and unrelated allogeneic SCT following reduced-intensity conditioning regimens.
引用
收藏
页码:4389 / 4396
页数:8
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