Second allo-SCT in patients with lymphoma relapse after a first allogeneic transplantation. A retrospective study of the EBMT Lymphoma Working Party

被引:14
|
作者
Horstmann, K. [1 ,2 ]
Boumendil, A. [1 ]
Finke, J. [3 ]
Finel, H. [1 ]
Kanfer, E. [4 ]
Milone, G. [5 ]
Russell, N. [6 ]
Bacigalupo, A. [7 ]
Chalandon, Y. [8 ,9 ]
Diez-Martin, J. L. [10 ]
Ifrah, N. [11 ]
Jurado Chacon, M. [2 ,12 ]
Dreger, P. [1 ,2 ]
机构
[1] EBMT Lymphoma Working Party, Paris, France
[2] Heidelberg Univ, Dept Med 5, D-69120 Heidelberg, Germany
[3] Univ Freiburg, Dept Med 1, D-79106 Freiburg, Germany
[4] Imperial Coll Healthcare NHS Trust, Hammersmith Hosp, London, England
[5] Azienda Osped Policlin Vittorio Emanuele, Programma Trapianto Emopoiet, Catania, Italy
[6] Univ Nottingham Hosp, Ctr Clin Hematol, Nottingham NG7 2UH, England
[7] IRCCS San Martino, Div Hematol & Bone Marrow Transplantat, Genoa, Italy
[8] Univ Hosp Geneva, Div Hematol, Dept Med Specialties, Geneva, Switzerland
[9] Univ Geneva, Fac Med, Geneva, Switzerland
[10] HGU Gregorio Maranon, Dept Hematol & Hemotherapy, Madrid, Spain
[11] CHRU, Serv Malad Sang, Angers, France
[12] Hosp Univ Virgen Ias Nieves, Granada, Spain
关键词
STEM-CELL TRANSPLANTATION; EUROPEAN GROUP; MARROW-TRANSPLANTATION; SOCIETE-FRANCAISE; ACUTE-LEUKEMIA; RISK; STRATEGY; BLOOD; INFUSIONS; SURVIVAL;
D O I
10.1038/bmt.2015.12
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The aim of this registry-based retrospective study was to analyze the outcome of second allogeneic hematopoietic SCT (alloHSCT_2) performed in patients with lymphoma who had relapsed after a first allogeneic transplant (alloHSCT_1). Patients >= 18 years who had received an alloHSCT_2 for lymphoma relapse between 2000 and 2011 were eligible. One hundred and forty patients were identified. The diagnosis was Hodgkin lymphoma (HL) in 31%, diffuse large B-cell lymphoma in 14%, T-cell lymphoma in 12%, indolent lymphoma in 19%, mantle cell lymphoma in 16% and other lymphomas in 8% of the patients. The median interval from alloHSCT_1 to alloHSCT_2 was 19 (range 4-116) months. Disease status at alloHSCT_2 was chemosensitive in 46%, refractory in 43% and unknown in 11% of the patients. Three-year PFS, OS, relapse incidence and nonrelapse mortality were 19%, 29%, 58% and 23%, respectively. PFS and OS were significantly affected by refractory disease at alloHSCT_2 and a short interval between alloHSCT_1 and alloHSCT_2. Long-term PFS was observed across all lymphoma subsets except for aggressive B-cell lymphoma. In conclusion, alloHSCT_2 is feasible and can result in long-term disease control in patients with lymphoma recurrence after alloHSCT_1, in particular if relapse occurs late and is chemosensitive.
引用
收藏
页码:790 / 794
页数:5
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