Alternative donor transplantation after reduced intensity conditioning: results of parallel phase 2 trials using partially HLA-mismatched related bone marrow or unrelated double umbilical cord blood grafts

被引:436
|
作者
Brunstein, Claudio G. [1 ]
Fuchs, Ephraim J. [2 ]
Carter, Shelly L. [3 ]
Karanes, Chatchada [4 ]
Costa, Luciano J. [5 ]
Wu, Juan [3 ]
Devine, Steven M. [6 ]
Wingard, John R. [7 ]
Aljitawi, Omar S. [8 ]
Cutler, Corey S. [9 ]
Jagasia, Madan H. [10 ]
Ballen, Karen K. [11 ]
Eapen, Mary [12 ]
O'Donnell, Paul V. [13 ]
机构
[1] Univ Minnesota, Blood & Marrow Transplant Program, Minneapolis, MN USA
[2] Johns Hopkins Univ, Sidney Kimmel Canc Ctr, Baltimore, MD USA
[3] Emmes Corp, Rockville, MD USA
[4] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[5] Med Univ S Carolina, Charleston, SC 29425 USA
[6] Ohio State Univ, Columbus, OH 43210 USA
[7] Univ Florida, Coll Med, Gainesville, FL USA
[8] Univ Kansas, Kansas City, KS USA
[9] Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Vanderbilt Univ, Nashville, TN USA
[11] Massachusetts Gen Hosp, Boston, MA 02114 USA
[12] Med Coll Wisconsin, Ctr Int Blood & Marrow Transplant Res, Milwaukee, WI 53226 USA
[13] Univ Washington, Fred Hutchinson Canc Ctr, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
STEM-CELL TRANSPLANTATION; ACUTE MYELOID-LEUKEMIA; POSTTRANSPLANTATION CYCLOPHOSPHAMIDE; HEMATOLOGIC MALIGNANCIES; FLUDARABINE; ENGRAFTMENT; OUTCOMES; ADULTS;
D O I
10.1182/blood-2011-03-344853
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Blood and Marrow Transplant Clinical Trials Network conducted 2 parallel multicenter phase 2 trials for individuals with leukemia or lymphoma and no suitable related donor. Reduced intensity conditioning (RIC) was used with either unrelated double umbilical cord blood (dUCB) or HLA-haploidentical related donor bone marrow (Haplo-marrow) transplantation. For both trials, the transplantation conditioning regimen incorporated cyclophosphamide, fludarabine, and 200 cGy of total body irradiation. The 1-year probabilities of overall and progression-free survival were 54% and 46%, respectively, after dUCB transplantation (n = 50) and 62% and 48%, respectively, after Haplo-marrow transplantation (n = 50). The day +56 cumulative incidence of neutrophil recovery was 94% after dUCB and 96% after Haplo-marrow transplantation. The 100-day cumulative incidence of grade II-IV acute GVHD was 40% after dUCB and 32% after Haplo-marrow transplantation. The 1-year cumulative incidences of non-relapse mortality and relapse after dUCB transplantation were 24% and 31%, respectively, with corresponding results of 7% and 45%, respectively, after Haplo-marrow transplantation. These multicenter studies confirm the utility of dUCB and Haplo-marrow as alternative donor sources and set the stage for a multicenter randomized clinical trial to assess the relative efficacy of these 2 strategies. The trials are registered at www.clinicaltrials.gov under NCT00864227 (BMT CTN 0604) and NCT00849147 (BMT CTN 0603). (Blood.2011;118(2):282-288)
引用
收藏
页码:282 / 288
页数:7
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