Long-term follow-up of reduced-intensity allogeneic stem cell transplantation for chronic lymphocytic leukemia: prognostic model to predict outcome

被引:87
|
作者
Brown, J. R. [1 ,2 ,3 ]
Kim, H. T. [1 ]
Armand, P. [1 ,2 ,3 ]
Cutler, C. [1 ,2 ,3 ]
Fisher, D. C. [1 ,2 ,3 ]
Ho, V. [1 ,2 ,3 ]
Koreth, J. [1 ,2 ,3 ]
Ritz, J. [1 ,2 ,3 ]
Wu, C. [1 ,2 ,3 ]
Antin, J. H. [1 ,2 ,3 ]
Soiffer, R. J. [1 ,2 ,3 ]
Gribben, J. G. [1 ,2 ,3 ]
Alyea, E. P. [1 ,2 ,3 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
CLL; RIC; myeloablative; SCT; prognostic model; BONE-MARROW-TRANSPLANTATION; PROGRESSION-FREE SURVIVAL; POOR-PROGNOSIS; INITIAL THERAPY; FLUDARABINE; RITUXIMAB; CYCLOPHOSPHAMIDE; GENE; CHEMOIMMUNOTHERAPY; MULTICENTER;
D O I
10.1038/leu.2012.228
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic lymphocytic leukemia (CLL) remains incurable with chemoimmunotherapy, and allogeneic hematopoietic stem cell transplantation (HSCT) offers the potential for cure. We assessed the outcomes of 108 CLL patients undergoing first allogeneic HSCTs, 76 with reduced-intensity (RIC) and 32 with myeloablative conditioning (MAC) between 1998 and 2009 at Dana-Farber Cancer Institute. With median follow-up of 5.9 years in surviving patients, the 5-year overall survival (OS) for the entire cohort is 63% for RIC regimens and 49% for MAC regimens (P=0.18). The risk of death declined significantly starting in 2004, and we found that 5-year OS for HSCT between 2004 and 2009 was 83% for RIC regimens compared with 47% for MAC regimens (P=0.003). For RIC transplantation, we developed a prognostic model based on predictors of progression-free survival (PFS), specifically remission status, lactate dehydrogenase, comorbidity score and lymphocyte count, and found 5-year PFS to be 83% for Score 0, 63% for Score 1, 24% for Score 2 and 6% for Score >= 3 (P<0.0001). We conclude that RIC HSCT for CLL in the current era is associated with excellent long-term PFS and OS, and, as potentially curative therapy, should be considered early in the disease course of relapsed high-risk CLL patients. Leukemia (2013) 27, 362-369; doi:10.1038/leu.2012.228
引用
收藏
页码:362 / 369
页数:8
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