Multi-state analysis illustrates treatment success after stem cell transplantation for acute myeloid leukemia followed by donor lymphocyte infusion

被引:34
|
作者
Eefting, Matthias [1 ]
de Wreede, Liesbeth C. [2 ]
Halkes, Constantijn J. M. [1 ]
von dem Borne, Peter A. [1 ]
Kersting, Sabina [1 ]
Marijt, Erik W. A. [1 ]
Veelken, Hendrik [1 ]
Putter, Hein [2 ]
Schetelig, Johannes [3 ]
Falkenburg, J. H. Frederik [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Hematol, NL-2300 RA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Med Stat & Bioinformat, NL-2300 RA Leiden, Netherlands
[3] DKMS, German Bone Marrow Donor Ctr, Munich, Germany
关键词
VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; FREE SURVIVAL; COMPETING RISKS; MYELODYSPLASTIC SYNDROMES; LEUKOCYTE INFUSIONS; RELAPSE; MODELS; EXPERIENCE; CHIMERISM;
D O I
10.3324/haematol.2015.136846
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the field of hematopoietic stem cell transplantation, the common approach is to focus outcome analyses on time to relapse and death, without assessing the impact of post-transplant interventions. We investigated whether a multi-state model would give insight into the events after transplantation in a cohort of patients who were transplanted using a strategy including scheduled donor lymphocyte infusions. Seventy-eight consecutive patients who underwent myeloablative T-cell depleted allogeneic stem cell transplantation for acute myeloid leukemia or myelodysplastic syndrome were studied. We constructed a multi-state model to analyze the impact of donor lymphocyte infusion and graft-versus-host disease on the probabilities of relapse and non-relapse mortality over time. Based on this model we introduced a new measure for outcome after transplantation which we called 'treatment success': being alive without relapse and immunosuppression for graft-versus-host disease. All relevant clinical events were implemented into the multi-state model and were denoted treatment success or failure ( either transient or permanent). Both relapse and non-relapse mortality were causes of failure of comparable magnitude. Whereas relapse was the dominant cause of failure from the transplantation state, its rate was reduced after graft-versus-host disease, and especially after donor lymphocyte infusion. The long-term probability of treatment success was approximately 40%. This probability was increased after donor lymphocyte infusion. Our multi-state model helps to interpret the impact of post-transplantation interventions and clinical events on failure and treatment success, thus extracting more information from observational data.
引用
收藏
页码:506 / 514
页数:9
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