Standard graft-versus-host disease prophylaxis with or without anti-T-cell globulin in haematopoietic cell transplantation from matched unrelated donors: a randomised, open-label, multicentre phase 3 trial

被引:579
作者
Finke, Juergen [1 ]
Bethge, Wolfgang A. [2 ]
Schmoor, Claudia [3 ]
Ottinger, Hellmut D. [4 ]
Stelljes, Matthias [5 ]
Zander, Axel R. [6 ]
Volin, Liisa [7 ]
Ruutu, Tapani [7 ]
Heim, Dominik A. [8 ]
Schwerdtfeger, Rainer [9 ]
Kolbe, Karin [10 ]
Mayer, Jiri [11 ]
Maertens, Johan A. [12 ]
Linkesch, Werner [13 ]
Holler, Ernst [14 ]
Koza, Vladimir [15 ]
Bornhaeuser, Martin [16 ]
Einsele, Hermann [17 ]
Kolb, Hans-Jochem [18 ]
Bertz, Hartmut [1 ]
Egger, Matthias [1 ]
Grishina, Olga [3 ]
Socie, Gerard [19 ]
机构
[1] Univ Freiburg Klinikum, Dept Hematol & Oncol, D-79106 Freiburg, Germany
[2] Univ Klinikum Tubingen, Dept Hematol & Oncol, Tubingen, Germany
[3] Clin Trials Ctr Univ Klinikum, Freiburg, Germany
[4] Univ Klinikum Essen, Klin & Poliklin KMT, Essen, Germany
[5] Univ Klin Munster, Dept Hematol & Oncol, Munster, Germany
[6] Univ Klinikum Hamburg Eppendorf, Dept Internal Med, Hamburg, Germany
[7] Univ Helsinki, Cent Hosp, Dept Med, FIN-00014 Helsinki, Finland
[8] Univ Spital Basel, Dept Hematol, Basel, Switzerland
[9] Stiftung Deutsch Klin Diagnost, Ctr Blood & Bone Marrow Transplantat, Wiesbaden, Germany
[10] Johannes Gutenberg Univ Mainz, Dept Internal Med, Univ Med, D-6500 Mainz, Germany
[11] Univ Hosp Brno, Dept Internal Med, Brno, Czech Republic
[12] IK UZ Gasthuisberg, Dept Hematol, Leuven, Belgium
[13] Univ Klinikum Graz, Dept Med Hematol, Graz, Austria
[14] Klinikum Univ Regensburg, Dept Hematol & Oncol, Regensburg, Germany
[15] Charles Univ Hosp, Dept Hematol & Oncol, Plzen, Czech Republic
[16] Univ Klinikum Carl Gustav Carus, Ctr Bone Marrow Transplantat, Dresden, Germany
[17] Univ Klin Wurzburg, Med Klin & Poliklin 2, Wurzburg, Germany
[18] Univ Munich, Klinikum Grosshadern, Dept Hematol, D-8000 Munich, Germany
[19] Hop St Louis, Serv Hematol Geffe de Moelle, Paris, France
关键词
BONE-MARROW-TRANSPLANTATION; TERM-FOLLOW-UP; ANTITHYMOCYTE GLOBULIN; COMPETING RISKS; CLINICAL-TRIALS; STEM-CELLS; DEPLETION; SURVIVAL; BLOOD; RECIPIENTS;
D O I
10.1016/S1470-2045(09)70225-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Graft-versus-host disease (GVHD) is a major cause of morbidity and mortality after allogeneic haematopoietic cell transplantation from unrelated donors. Anti-T-cell globulins (ATGs) might lower the incidence of GVHD. We did a prospective, randomised, multicentre, open-label, phase 3 trial to compare standard GVHD prophylaxis with ciclosporin and methotrexate with or without anti-Jurkat ATG-Fresenius (ATG-F). Methods Between May 26, 2003, and Feb 8, 2007, 202 patients with haematological malignancies were centrally randomly assigned using computer-generated centre-stratified block randomisation between treatment groups receiving ciclosporin and methotrexate with or without additional ATG-F. One patient in the ATG-F group did not undergo transplantation, thus 201 patients who underwent transplantation with peripheral blood (n=164; 82%) or bone marrow (n=37; 18%) grafts from unrelated donors after myeloablative conditioning were included in the fun analysis set, and were analysed according to their randomly assigned treatment (ATG-F n=103, control n=98). The primary endpoint was severe acute GVHD (aGVHD) grade III-IV or death within 100 days of transplantation. The trial is registered with the numbers DRKS00000002 and NCT00655343. Findings The number of patients in the ATG-F group who had severe aGVHD grade III-IV or who died within 100 days of transplantation was 12 and 10 (21.4%, 95% CI 13.4-29.3), respectively, compared with 24 and nine (33.7%, 24.3-43.0) patients, respectively, in the control group (adjusted odds ratio 0.59, 95% CI 0.30-1.17; p=0.13). The cumulative incidence of aGVHD grade III-IV was 11.7% (95% CI 6.8-19.8) in the ATG-F group versus 24-5% (17.3-34.7) in the control group (adjusted hazard ratio [HR] 0.50, 95% CI 0.25-1.01; p=0.054), and cumulative incidence of aGVHD grade II-IV was 33.0% (n=34; 95% CI 25.1-43.5) in the ATG-F group versus 51.0% (n=50; 95% CI 42.0-61.9) in the control group (adjusted HR 0.56, 0.36-0.87; p=0.011). The 2-year cumulative incidence of extensive chronic GVHD was 12.2% (n=11; 95% CI 7.0-21.3) versus 42.6% (n=34; 95% CI 33.0-55.0; adjusted HR 0.22, 0.11-0.43; p<0.0001). There were no differences between treatment groups with regard to relapse, non-relapse mortality, overall survival, and mortality from infectious causes. Interpretation The addition of ATG-F to GVHD prophylaxis with ciclosporin and methotrexate resulted in decreased incidence of acute and chronic GVHD without an increase in relapse or non-relapse mortality, and without compromising overall survival. The use of ATG-F is safe for patients who are going to receive a haernatopoietic cell transplantation from matched unrelated donors.
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收藏
页码:855 / 864
页数:10
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