Post-transplantation Cyclophosphamide and Sirolimus after Haploidentical Hematopoietic Stem Cell Transplantation Using a Treosulfan-based Myeloablative Conditioning and Peripheral Blood Stem Cells

被引:112
|
作者
Cieri, Nicoletta [1 ,2 ]
Greco, Raffaella [1 ]
Crucitti, Lara [1 ,3 ]
Morelli, Mara [1 ]
Giglio, Fabio [1 ]
Levati, Giorgia [1 ]
Assanelli, Andrea [1 ]
Carrabba, Matteo G. [1 ]
Bellio, Laura [4 ]
Milani, Raffaella [4 ]
Lorentino, Francesca [1 ]
Stanghellini, Maria Teresa Lupo [1 ]
De Freitas, Tiago [1 ]
Marktel, Sarah [1 ]
Bernardi, Massimo [1 ]
Corti, Consuelo [1 ]
Vago, Luca [1 ,3 ]
Bonini, Chiara
Ciceri, Fabio [1 ,3 ]
Peccatori, Jacopo [1 ]
机构
[1] Ist Sci San Raffaele, Hematol & Bone Transplantat Unit, Div Regenerat Med Stem Cells & Gene Therapy, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, Expt Hematol Unit, Div Immunol Transplantat & Infect Dis, I-20132 Milan, Italy
[3] Ist Sci San Raffaele, Mol & Funct Immunogenet Unit, Div Regenerat Med Stem Cells & Gene Therapy, I-20132 Milan, Italy
[4] Ist Sci San Raffaele, Immunohematol & Transfus Med Unit, Div Regenerat Med Stem Cells & Gene Therapy, I-20132 Milan, Italy
关键词
Post-transplantation cyclophosphamide; Sirolimus; Peripheral blood stem cell transplantation; Allogeneic stem cell transplantation; Haploidentical transplantation; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; HUMAN-LEUKOCYTE ANTIGEN; REGULATORY T-CELLS; HIGH-RISK; ACUTE-LEUKEMIA; HEMATOLOGIC MALIGNANCIES; MISMATCHED HLA; PHASE-II; RAPAMYCIN;
D O I
10.1016/j.bbmt.2015.04.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Haploidentical hematopoietic stem cell transplantation (HSCT) performed using bone marrow (BM) grafts and post-transplantation cyclophosphamide (PTCy) has gained much interest for the excellent toxicity profile after both reduced-intensity and myeloablative conditioning. We investigated, in a cohort of 40 high-risk hematological patients, the feasibility of peripheral blood stem cells grafts after a treosulfan-melphalan myeloablative conditioning, followed by a PTCy and sirolimus-based graft-versus-host disease (GVHD) prophylaxis (Sir-PTCy). Donor engraftment occurred in all patients, with full donor chimerism achieved by day 30. Post-HSCT recovery of lymphocyte subsets was broad and fast, with a median time to CD4 > 200/mu L of 41 days. Cumulative incidences of grade II to IV and III-IV acute GVHD were 15% and 7.5%, respectively, and were associated with a significant early increase in circulating regulatory T cells at day 15 after HSCT, with values < 5% being predictive of subsequent GVHD occurrence. The 1-year cumulative incidence of chronic GVHD was 20%. Nonrelapse mortality (NRM) at 100 days and 1 year were 12% and 17%, respectively. With a median follow-up for living patients of 15 months, the estimated 1-year overall and disease-free survival (DFS) was 56% and 48%, respectively. Outcomes were more favorable in patients who underwent transplantation in complete remission (1-year DFS 71%) versus patients who underwent transplantation with active disease (DFS, 34%; P = .01). Overall, myeloablative haploidentical HSCT with peripheral blood stem cells (PBSC) and Sir-PTCy is a feasible treatment option: the low rates of GVHD and NRM as well as the favorable immune reconstitution profile pave the way for a prospective comparative trial comparing BM and PBSC in this specific transplantation setting. (C) 2015 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1506 / 1514
页数:9
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