Thymoglobulin prevents chronic graft-versus-host disease, chronic lung dysfunction, and late transplant-related mortality: Long-term follow-up of a randomized trial in patients undergoing unrelated donor transplantation

被引:284
作者
Bacigalupo, A
Lamparelli, T
Barisione, G
Bruzzi, P
Guidi, S
Alessandrino, PE
di Bartolomeo, P
Oneto, R
Bruno, B
Sacchi, N
van Lint, MT
Bosi, A
机构
[1] Osped San Martino Genova, Div Ematol, Genoa, Italy
[2] Osped San Martino Genova, UO Med Prevent & Lavoro Lab Fisiopatol Resp, Genoa, Italy
[3] Osped San Martino Genova, IST, Genoa, Italy
[4] Osped Careggi, Dipartimento Ematol, Florence, Italy
[5] Policlin San Matteo, Dipartimento Ematol, I-27100 Pavia, Italy
[6] Osped Civille, Dipartimento Ematol, Pescara, Italy
[7] Osped Galliera, IBMDR, Genoa, Italy
关键词
leukemia; bone marrow transplantation; unrelated donors; aantithymocyte globulin; chronic lung dysfunction;
D O I
10.1016/j.bbmt.2005.12.034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This is an update of a randomized study on antithymocyte globulin (ATG; Thymoglobulin) before transplantation in patients undergoing unmanipulated marrow transplantation from unrelated donors. The median follow-up for surviving patients is 5.7 years. At last follow-up, chronic graft-versus-host disease (GVHD),vas scored in 60% of non-ATG and in 37% of ATG patients (P=.05), and extensive chronic GVHD was present in 41% and 15%, respectively (P=.01). Chronic lung dysfunction was diagnosed in 51% versus 19% of patients (P=.005). Forced vital capacity decreased significantly with time in non-ATG patients (P=.005), but not in patients who received ATG (P=.30). The proportion of patients with Karnofsky scores of >= 90% at 4 years was 57% versus 89% in non-ATG versus ATG patients (P=.03). The actuarial 6-year survival for all patients randomized was 31% versus 44% (non-ATG versus ATG; P=.80). The cumulative incidence of transplant-related mortality was 51% versus 41% (P=.70) and of relapse was 32% versus 40% (P=.90). For patients who survived 1 year, transplant-related mortality was 25% versus 3% (P=.03), and actuarial survival was 58% versus 85% (P=.09). In conclusion, the addition of ATG to cyclosporine/methotrexate provides significant protection against extensive chronic GVHD and chronic lung dysfunction, reduces late transplant mortality, and improves quality of life in patients undergoing unrelated donor transplantation. (C) 2006 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:560 / 565
页数:6
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