Comparison of haploidentical and umbilical cord blood transplantation after myeloablative conditioning

被引:20
作者
Wagner, John E., Jr. [1 ]
Ballen, Karen K. [2 ]
Zhang, Mei-Jie [3 ]
Allbee-Johnson, Mariam [4 ]
Karanes, Chatchada [5 ]
Milano, Filippo [6 ]
Verneris, Michael R. [7 ]
Eapen, Mary [4 ]
Brunstein, Claudio G. [1 ]
机构
[1] Univ Minnesota, Blood & Marrow Transplant Program, Mayo Mail Code 480,420 Delaware St SE, Minneapolis, MN 55455 USA
[2] Univ Virginia, Sch Med, Div Hematol Oncol, Charlottesville, VA 22908 USA
[3] Med Coll Wisconsin, Div Biostat, Inst Heath & Equ, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Med, Ctr Int Blood & Marrow Transplant Res, Milwaukee, WI 53226 USA
[5] City Hope Natl Med Ctr, Dept Hematol Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
[6] Fred Hutchinson Canc Res Ctr, Clin Res Div, 1124 Columbia St, Seattle, WA 98104 USA
[7] Univ Colorado, Sch Med, Dept Pediat, Ctr Canc & Blood Disorders,Bone Marrow Transplant, Denver, CO USA
基金
美国国家卫生研究院;
关键词
STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; ALTERNATIVE DONOR TRANSPLANTATION; HEMATOLOGIC MALIGNANCIES; ALLOGENEIC MARROW; LEUKEMIA; SURVIVAL; ENGRAFTMENT; OUTCOMES;
D O I
10.1182/bloodadvances.2021004462
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) has emerged as an important treatment modality. Most reports comparing haplo-HSCT with posttransplant cyclophosphamide (PTCy) and other donor sources have focused on outcomes in older adults treated with reduced intensity conditioning. Therefore, in the current study, we evaluated outcomes in patients with hematological malignancy treated with myeloablative conditioning prior to haplo- (n = 375) or umbilical cord blood (UCB; n = 333) HSCT. All haplo recipients received a 4 of 8 HLA-matched graft, whereas recipients of UCB were matched at 6-8/8 (n = 145) or <_5/8 (n = 188) HLA antigens. Recipients of 6-8/8 UCB transplants were younger (14 years vs 21 and 29 years) and more likely to have lower comorbidity scores compared with recipients of <_5/8 UCB and haplo-HSCT (81% vs 69% and 63%, respectively). UCB recipients were more likely to have acute lymphoblastic leukemia and transplanted in second complete remission (CR), whereas haplo-HSCT recipients were more likely to have acute myeloid leukemia in the first CR. Other characteristics, including cytogenetic risk, were similar. Survival at 3 years was similar for the donor sources (66% haplo- and 61% after <_5/8 and 58% after 6-8/8 UCB). Notably, relapse at 3 years was lower in recipients of <_5/8 UCB (21%, P = .03) compared with haplo- (36%) and 6-8/8 UCB (30%). However, nonrelapse mortality was higher in <_5/8 UCB (21%) compared with other groups (P < .0001). These data suggest that haplo-HSCT with PTCy after myeloablative conditioning provides an overall survival outcome comparable to that after UCB regardless HLA match group.
引用
收藏
页码:4064 / 4072
页数:9
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