Outcome of patients developing GVHD after DLI given to treat CML relapse: a study by the chronic leukemia working party of the EBMT

被引:51
作者
Chalandon, Y. [1 ]
Passweg, J. R.
Schmid, C. [2 ]
Olavarria, E. [3 ]
Dazzi, F. [3 ]
Simula, M. P. [3 ]
Ljungman, P. [4 ]
Schattenberg, A. [5 ]
de Witte, T. [5 ]
Lenhoff, S. [6 ]
Jacobs, P. [7 ,8 ]
Volin, L. [9 ]
Iacobelli, S. [10 ,11 ]
Finke, J. [12 ]
Niederwieser, D. [13 ]
Guglielmi, C. [14 ]
机构
[1] Univ Hosp Geneva, Hematol Serv, Dept Internal Med, Div Hematol, CH-1211 Geneva 14, Switzerland
[2] Klinikum Augsburg II, Med Klin, Augsburg, Germany
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Haematol, London, England
[4] Karolinska Univ Hosp, Huddinge Haematol Ctr, Huddinge, Sweden
[5] Radboud Univ Nijmegen, Dept Hematol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[6] Univ Lund Hosp, Dept Hematol, S-22185 Lund, Sweden
[7] Groote Schuur Hosp, Dept Haematol, ZA-7925 Cape Town, South Africa
[8] Searl Lab Cellular & Mol Biol, BMT Unit, Constantiaberg Medi Clin, Cape Town, South Africa
[9] Univ Helsinki, Cent Hosp, Dept Med, Helsinki, Finland
[10] Univ Molise, Dipartimento Sci Salute, Rome, Italy
[11] Dept Biostat & Med Informat, Chron Leukaemia WP Registry, Leiden, Netherlands
[12] Univ Freiburg, Dept Med Hematol, Freiburg, Germany
[13] Univ Leipzig, Div Haematol & Oncol, Leipzig, Germany
[14] Univ Roma La Sapienza, Fac Med 2, UOC Ematol AOS Andrea, Rome, Italy
基金
英国医学研究理事会;
关键词
DLI; relapse; CML; GVHD; allo-SCT; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; DONOR LEUKOCYTE INFUSIONS; ADOPTIVE IMMUNOTHERAPY; LYMPHOCYTE INFUSIONS; RISK-FACTORS; GRAFT; METHOTREXATE;
D O I
10.1038/bmt.2009.177
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We studied GVHD after donor lymphocyte infusion (DLI) in 328 patients with relapsed CML between 1991 and 2004. A total of 122 patients (38%) developed some form of GVHD. We analyzed GVHD by clinical presentation (acute or chronic GVHD) and onset time after the first DLI (early (<= 45 days) or late (>45 days)). There was a significant overlap between onset time and clinical presentation. Some form of GVHD occurred at a median of 104 days, acute GVHD at 45 days and chronic GVHD at 181 days after DLI. The clinical presentation was acute GVHD in 71 patients, of whom 31 subsequently developed chronic GVHD subsequently. De novo chronic GVHD was seen in 51 patients. OS for all patients was 69% (95% confidence interval (CI) 63-75) at 5 years, DLI-related mortality was 11% (95% CI 8-15) and disease-related mortality was 20% (95% CI 16-25). Risk factors for developing GVHD after DLI were T-cell dose at first DLI, the time interval from transplant to DLI and donor type. In time-dependent multivariate analysis, GVHD after DLI was associated with a risk of death of 2.3-fold compared with patients without GVHD. Clinical presentation as acute GVHD and early onset GVHD were associated with increased mortality.
引用
收藏
页码:558 / 564
页数:7
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