Donor lymphocyte infusion for relapsed chronic myelogenous leukemia: prognostic relevance of the initial cell dose

被引:131
作者
Guglielmi, C
Arcese, W
Dazzi, F
Brand, R
Bunjes, D
Verdonck, LF
Schattenberg, A
Kolb, HJ
Ljungman, P
Devergie, A
Bacigalupo, A
Gomez, M
Michallet, M
Elmaagacli, A
Gratwohl, A
Apperley, J
Niederwieser, D
机构
[1] Univ Roma La Sapienza, Cattedra Ematol, Dipartimento Biotecnol Cellulari & Ematol, Unita TMO Allogenico Giuseppe Papa, I-00161 Rome, Italy
[2] Univ London Imperial Coll Sci Technol & Med, Sch Med, Hammersmith Hosp, Dept Hematol, London, England
[3] Leiden Univ, Med Ctr, Dept Med Stat, Leiden, Netherlands
[4] Univ Ulm, Abt Innere Med 3, Ulm, Germany
[5] Univ Utrecht, Med Ctr, Dept Hematol, Utrecht, Netherlands
[6] Univ Nijmegen, Med Ctr St Radboud, Nijmegen, Netherlands
[7] Univ Munich, Klinikum Grosshadern, Med Klin 3, D-8000 Munich, Germany
[8] Huddinge Univ Hosp, Stockholm, Sweden
[9] Hop St Louis, Dept Hematol & Bone Marrow Transplantat, Paris 10, France
[10] Osped San Martino Genova, Dept Hematol, Genoa, Italy
[11] Hosp Clin Barcelona, IDIBAPS, Dept Hematol, Bone Marrow Transplantat Sect, Barcelona, Spain
[12] Hop Edouard Herriot, Bone Marrow Transplant Unit, Lyon 03, France
[13] Univ Hosp Essen, Dept Bone Marrow Transplant, Essen, Germany
[14] Kantonsspital Basel, Dept Internal Med, Div Hematol, Basel, Switzerland
[15] Univ Leipzig, Ctr Internal Med, Dept Hematol Oncol, Leipzig, Germany
关键词
D O I
10.1182/blood.V100.2.397
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Donor lymphocyte infusion (DLI) can produce durable remissions in patients with chronic myelogenous leukemia (CML) who have a relapse after an allogenelc stem cell transplantation. However, the best modality to administer DLI is still unclear. The effect of the initial cell dose (ICD; le, mononuclear cells x 10(8)/kg received In the first instance) on outcome was retrospectively analyzed in 298 of 344 patients treated with DLI at 51 centers. Patients were classified into 3 groups according to the ICD: 98 in group A (less than or equal to 0.20),107 In group B (0.21-2.0), and 93 In group C (> 2.0). Additional infusions were given to 62%, 20%, and 5% of patients in groups A, B, and C, respectively. A lower ICD was associated with less graft-versus-host disease (GVHD; A, 26%; B, 53%; C, 62%; P <.001), less myelosuppression (A, 10%; B, 23%; C, 24%; P=.01), and similar response rate (A, 78%; B, 73%; C, 70%; P=.48). Nonadjusted estimates of 3-year survival, failure-free survival, and DLI-related mortality were 84%, 66%, and 5% respectively, in group A; 63%, 57%, and 20% in group B; and 58%, 45%, and 22% in group C. Outcome analysis was adjusted for patient age, donor type, sex of donor, sex mis-match, disease phase at transplantation, T-cell depletion, interval from transplantation to DLI, GVHD prior to relapse, relapse type, and date of DLI. After adjustment, lower ICD was associated with less GVHD, less myelosuppression, same response rate, better survival, better failure-free survival, and less DLI-related mortality. Our results suggest that the first DLI dose should not exceed 0.2 X 10(8) mononuclear cells/kg. (Blood. 2002;100:397-405). (C) 2002 by The American Society of Hematology.
引用
收藏
页码:397 / 405
页数:9
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