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供者淋巴细胞输注治疗异基因造血细胞移植后复发的血液系统恶性肿瘤:初始 CD3+T 细胞剂量的预后相关性。

Donor lymphocyte infusion for relapsed hematological malignancies after allogeneic hematopoietic cell transplantation: prognostic relevance of the initial CD3+ T cell dose.

机构信息

Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.

出版信息

Biol Blood Marrow Transplant. 2013 Jun;19(6):949-57. doi: 10.1016/j.bbmt.2013.03.001. Epub 2013 Mar 21.

DOI:10.1016/j.bbmt.2013.03.001
PMID:23523892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3846289/
Abstract

The impact of donor lymphocyte infusion (DLI) initial cell dose on its outcome is known in patients with chronic myeloid leukemia but limited in patients with other hematological malignancies. In this retrospective study, we evaluated the effect of initial DLI CD3(+) cell dose on graft-versus-host disease (GVHD) and overall survival after DLI given for relapse of any hematological malignancies after allogeneic hematopoietic cell transplantation (HCT) with high- or reduced-intensity conditioning. The cohort included 225 patients. Initial DLI CD3(+) cell dose per kilogram of recipient body weight was ≤ 1 × 10(7) (n = 84; group A), >1.0 to <10 × 10(7) (n = 58; group B), and ≥ 10 × 10(7) (n = 66; group C). The initial cell dose was unknown for the remaining 17 patients. Cumulative incidence rates of GVHD at 12 months after DLI were 21%, 45%, and 55% for groups A, B, and C, respectively. Multivariate analysis showed that initial DLI CD3(+) cell ≥ 10 × 10(7) dose per kilogram is associated with an increased risk of GVHD after DLI (P = .03). Moreover, an initial DLI CD3(+) cell dose of 10 × 10(7) or higher did not decrease the risk of relapse and did not improve overall survival. Thus, these results support the use of less than 10 × 10(7) CD3(+) cell per kilogram as the initial cell dose of DLI for treatment of persistent or recurrent hematological malignancy after HCT.

摘要

供者淋巴细胞输注(DLI)初始细胞剂量对其疗效的影响在慢性髓性白血病患者中是已知的,但在其他血液恶性肿瘤患者中则有限。在这项回顾性研究中,我们评估了初始 DLI CD3(+)细胞剂量对异基因造血细胞移植(HCT)后接受高或低强度预处理的任何血液恶性肿瘤复发后给予 DLI 时移植物抗宿主病(GVHD)和总生存的影响。该队列包括 225 名患者。初始 DLI CD3(+)细胞剂量/受者体重≤1×10(7)(n=84;A 组)、>1.0 至<10×10(7)(n=58;B 组)和≥10×10(7)(n=66;C 组)。其余 17 名患者的初始细胞剂量未知。DLI 后 12 个月时 GVHD 的累积发生率分别为 A、B 和 C 组的 21%、45%和 55%。多变量分析显示,DLI 初始 CD3(+)细胞≥10×10(7)剂量/千克与 DLI 后 GVHD 的风险增加相关(P=0.03)。此外,初始 DLI CD3(+)细胞剂量为 10×10(7)或更高并不能降低复发风险,也不能改善总生存。因此,这些结果支持在 HCT 后治疗持续性或复发性血液恶性肿瘤时使用小于 10×10(7) CD3(+)细胞/千克作为 DLI 的初始细胞剂量。

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