Intensification of GVHD prophylaxis with low-dose ATG-F before allogeneic PBSC transplantation from HLA-identical siblings in adult patients with hematological malignancies: results from a retrospective analysis

被引:21
作者
Bonifazi, F. [1 ]
Bandini, G. [1 ]
Arpinati, M. [1 ]
Tolomelli, G. [1 ]
Stanzani, M. [1 ]
Motta, M. R. [1 ]
Rizzi, S. [1 ]
Giudice, V. [2 ]
Dan, E. [1 ]
Massari, E. [1 ]
Tazzari, P. [2 ]
Bontadini, A. [3 ]
Pagliaro, P. [2 ]
Baccarani, M. [1 ]
机构
[1] Univ Bologna, St Orsola Malpighi Hosp, Inst Hematol & Med Oncol, I-40138 Bologna, Italy
[2] St Orsola Malpighi Hosp, Dept Transfus Med, Bologna, Italy
[3] St Orsola Malpighi Hosp, Immunogenet Unit, Bologna, Italy
关键词
GVHD; hematopoietic SCT; TRM; ATG; sibling transplants; VERSUS-HOST-DISEASE; STEM-CELL TRANSPLANTATION; BLOOD PROGENITOR-CELL; BONE-MARROW-TRANSPLANTATION; PERIPHERAL-BLOOD; ANTITHYMOCYTE GLOBULIN; MYELOID-LEUKEMIA; UNRELATED DONORS; MOBILIZED BLOOD; EUROPEAN GROUP;
D O I
10.1038/bmt.2011.225
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Several studies have shown that chronic GVHD (cGVHD) is more frequent in patients receiving transplants from PBSC than in those receiving BM. In the setting of PBSC-unrelated transplants, the addition of anti-T-cell globulin (ATG) has shown a significant decrease in incidence/severity of cGVHD, without an increase in relapses or infections. However, no prospective data are yet available in the sibling setting. We retrospectively analyzed the effects of intensification of standard GVHD prophylaxis (CsA+MTX) by the addition of low-dose ATG in 245 patients receiving a transplant from HLA-identical sibling. From 1996 to 2001, patients received PBSC as the preferred source (group 2), and then ATG was added before transplant (group 3) because of a high cGVHD rate. Patients receiving BM in the same time period were analyzed as a control group (group 1). The incidence of grade III-IV acute GVHD and cGVHD was not significantly different in the three groups, but extensive cGVHD was highest in group 2 (38%) compared with group 3 (21%) or group 1 (28%; P=0.03). OS, TRM and time to relapse/progression were similar in the three groups. Our analysis shows that adding ATG to PBSC sibling allogeneic transplants can lower cGVHD, without an increase of relapse. Further prospective studies are needed to confirm these findings.
引用
收藏
页码:1105 / 1111
页数:7
相关论文
共 43 条
[1]   Allogeneic peripheral blood stem-cell compared with bone marrow transplantation in the management of hematologic malignancies: An individual patient data meta-analysis of nine randomized trials [J].
al-Jurf, M ;
Aranha, F ;
Annassetti, C ;
Apperley, JF ;
Baynes, R ;
Bensinger, WI ;
Blaise, D ;
Chaudhary, MA ;
Clarke, M ;
Cornelissen, JJ ;
Couban, S ;
Cutler, C ;
Djulbegovic, B ;
Gyger, M ;
Gratwohl, A ;
Heldal, D ;
Van der Holt, B ;
Hozo, I ;
Kuentz, M ;
Kumar, A ;
Lipton, J ;
Matchamm, J ;
Mohty, M ;
Morton, J ;
Panzarella, T ;
Powles, R ;
Richards, SM ;
Sahovic, E ;
Schmitz, N ;
Simpson, DR ;
Sirohi, B ;
Soares, HP ;
de Souza, CA ;
Vigorito, AC ;
Wheatley, K .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (22) :5074-5087
[2]   ANALYSIS OF SURVIVAL BY TUMOR RESPONSE [J].
ANDERSON, JR ;
CAIN, KC ;
GELBER, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (11) :710-719
[3]   Extended mycophenolate mofetil and shortened cyclosporine failed to reduce graft-versus-host disease after unrelated hematopoietic cell transplantation with nonmyeloablative conditioning [J].
Baron, Frederic ;
Sandmaier, Brenda M. ;
Storer, Barry E. ;
Maris, Michael B. ;
Langston, Amelia A. ;
Lange, Thoralf ;
Petersdorf, Effie ;
Bethge, Wolfgang ;
Maziarz, Richard T. ;
McSweeney, Peter A. ;
Pulsipher, Michael A. ;
Wade, Fames C. ;
Chauncey, Thomas R. ;
Sbizuru, Fudith A. ;
Sorror, Mohamed L. ;
Woolfrey, Ann E. ;
Maloney, David G. ;
Storb, Rainer .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (09) :1041-1048
[4]   Antithymocyte globulin for the prevention of graft-versus-host disease after unrelated hematopoietic stem cell transplantation for acute myeloid leukemia: results from the multicenter German cooperative study group [J].
Basara, N ;
Baurmann, H ;
Kolbe, K ;
Yaman, A ;
Labopin, M ;
Burchardt, A ;
Huber, C ;
Fauser, AA ;
Schwerdtfeger, R .
BONE MARROW TRANSPLANTATION, 2005, 35 (10) :1011-1018
[5]   Individual patient data meta-analysis of allogeneic peripheral blood stem cell transplant vs bone marrow transplant in the management of hematological malignancies: indirect assessment of the effect of day 11 methotrexate administration [J].
Bensinger, W. .
BONE MARROW TRANSPLANTATION, 2006, 38 (08) :539-546
[6]   TRANSPLANTATION OF ALLOGENEIC PERIPHERAL-BLOOD STEM-CELLS MOBILIZED BY RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR [J].
BENSINGER, WI ;
WEAVER, CH ;
APPELBAUM, FR ;
ROWLEY, S ;
DEMIRER, T ;
SANDERS, J ;
STORB, R ;
BUCKNER, CD .
BLOOD, 1995, 85 (06) :1655-1658
[7]   Allogeneic peripheral blood stem cell transplantation in patients with advanced hematologic malignancies: A retrospective comparison with marrow transplantation [J].
Bensinger, WI ;
Clift, R ;
Martin, P ;
Appelbaum, FR ;
Demirer, T ;
Gooley, T ;
Lilleby, K ;
Rowley, S ;
Sanders, J ;
Storb, R ;
Buckner, CD .
BLOOD, 1996, 88 (07) :2794-2800
[8]   Randomized trial of bone marrow versus lenograstim-primed blood cell allogeneic transplantation in patients with early-stage leukemia: A report from the Societe Francaise de Greffe de Moelle [J].
Blaise, D ;
Kuentz, M ;
Fortanier, C ;
Bourhis, JH ;
Milpied, N ;
Sutton, L ;
Jouet, JP ;
Attal, M ;
Bordigoni, P ;
Cahn, JY ;
Boiron, JM ;
Schuller, MP ;
Moatti, JP ;
Michalle, M .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (03) :537-546
[9]   In vivo T-cell depletion with low-dose ATG is effective in reducing cGVHD after peripheral blood stem cell myeloablative sibling transplants in CML:: results from a prospective phase II study [J].
Bonifazi, F ;
Bandini, G ;
Stanzani, M ;
Palandri, F ;
Giannini, B ;
Arpinati, M ;
Rosti, G ;
Baccarani, M .
BONE MARROW TRANSPLANTATION, 2005, 35 (10) :1025-1026
[10]  
Champlin RE, 2000, BLOOD, V95, P3702