A conditioning platform based on fludarabine, busulfan, and 2 days of rabbit antithymocyte globulin results in promising results in patients undergoing allogeneic transplantation from both matched and mismatched unrelated donor

被引:23
作者
Devillier, Raynier [1 ,2 ,3 ]
Fuerst, Sabine [1 ]
Crocchiolo, Roberto [1 ]
El-Cheikh, Jean [1 ]
Castagna, Luca [1 ,4 ]
Harbi, Samia [1 ]
Granata, Angela [1 ]
D'Incan, Evelyne [1 ]
Coso, Diane [1 ]
Chabannon, Christian [2 ,3 ,5 ,6 ]
Picard, Christophe [7 ]
Etienne, Anne [1 ]
Calmels, Boris [5 ,6 ]
Schiano, Jean-Marc [1 ]
Lemarie, Claude [5 ,6 ]
Stoppa, Anne-Marie [1 ]
Bouabdallah, Reda [1 ]
Vey, Norbert [1 ,2 ,3 ]
Blaise, Didier [1 ,2 ,3 ]
机构
[1] Inst J Paoli I Calmettes, Unite Transplantat & Therapie Cellulaire, Dept Oncohematol, F-13273 Marseille 9, France
[2] Aix Marseille Univ, F-13007 Marseille, France
[3] Ctr Rech Cancerol Marseille, INSERM, UMR1068, F-13009 Marseille, France
[4] Inst Clinico Humanitas, Humanitas Canc Ctr, Hematol Unit, Milan, Italy
[5] Inst J Paoli I Calmettes, Ctr Therapie Cellulaire, Cell Therapy Facil, F-13273 Marseille 9, France
[6] Ctr Invest Clin Biotherapie, Inserm CBT 510, F-13009 Marseille, France
[7] EFS Alpes Mediterrannee, Lab Histocompatibil, Marseille, France
关键词
STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; HEMATOLOGIC DISEASES; CHRONIC GRAFT; RISK; THERAPY; RECIPIENTS; SIBLINGS; LEUKEMIA;
D O I
10.1002/ajh.23592
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Conditioning regimen including fludarabine, intravenous busulfan (Bx), and 5 mg/kg total dose of rabbit antithymocyte globulin (r-ATG) (FBx-ATG) results in low incidence of graft-versus-host disease (GVHD) and non-relapse mortality (NRM) after allogeneic hematopoietic stem cell transplantation (Allo-HSCT) from HLA-matched related or unrelated donors (MUD). However, whether this platform produces similar results in the setting of one mismatch unrelated donor (MMUD) Allo-HSCT is not known. We retrospectively analyzed patients aged less than 65 years who were diagnosed with hematological malignancies and received FBx-ATG regimen prior to Allo-HSCT from MUD (N=74) or MMUD (N=40). We compared outcome of MUD versus MMUD patients. There was no difference in the cumulative incidence of grades II-IV acute GVHD (MUD: 34% vs. MMUD: 35%, P=0.918), but MMUD patients developed more grade III-IV acute GVHD (MUD: 5% vs. MMUD: 15%, P=0.016). The cumulative incidences of overall chronic GVHD (MUD: 33% vs. MMUD: 22%, P=0.088) and extensive chronic GVHD (MUD: 20% vs. MMUD: 19%, P=0.594) were comparable. One-year NRM was similar in both groups (MUD: 16% vs. MMUD: 14%, P=0.292); similarly, progression-free survival (MUD: 59% vs. MMUD: 55%, P=0.476) and overall survival (MUD: 63% vs. MMUD: 61%, P=0.762) were not different between both groups. With a median follow up of 24 months, 35 of 74 MUD patients (47%) and 19 of 40 MMUD patients (48%) were free of both disease progression and immunosuppressive treatment. We conclude that the FBx-ATG regimen results in low incidences of NRM and GVHD in both MUD and the MMUD recipients. Am. J. Hematol. 89:83-87, 2014. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:83 / 87
页数:5
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