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接受去除CD8的供体淋巴细胞输注治疗异基因祖细胞移植后复发的慢性粒细胞白血病患者的长期随访

Long-Term follow-up of recipients of CD8-depleted donor lymphocyte infusions for the treatment of chronic myelogenous leukemia relapsing after allogeneic progenitor cell transplantation.

作者信息

Shimoni A, Gajewski J A, Donato M, Martin T, O'Brien S, Talpaz M, Cohen A, Korbling M, Champlin R, Giralt S

机构信息

Department of Blood and Bone Marrow Transplantation, University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Biol Blood Marrow Transplant. 2001;7(10):568-75. doi: 10.1016/s1083-8791(01)70017-1.

DOI:10.1016/s1083-8791(01)70017-1
PMID:11760089
Abstract

Donor lymphocyte infusions (DLIs) are an effective treatment for relapsed Chronic myeloid leukemia (CML) after allogeneic transplantation but are limited by the occurrence of GVHD. CD8+ T lymphocytes are involved in the pathogenesis of GVHD but may not be essential for the graft-versus-leukemia (GVL) effect in CML. We have treated 26 CML patients with posttransplantation relapse with CD8-depleted DLI. Thirteen of 15 patients (87%) who relapsed in early-phase CML achieved complete cytogenetic response, but only 1 of 11 who relapsed in advanced-phase disease achieved complete response. Acute GVHD occurred in 2 patients (8%), and extensive chronic GVHD occurred in 2 patients (11%). Treatment-related mortality was 11.5%. Responses were durable; with a median follow-up of 4.2 years (1-7.5 years), only 1 responding patient relapsed (7%). CD8-depleted DLI was equally effective and safe after unrelated donor transplants and sibling transplants. Cytogenetic clonal evolution at the time of DLI was not predictive of treatment failure unless associated with hematologic criteria for disease acceleration. CD8 depletion is an effective method to separate GVL from GVHD for posttransplantation relapsed CML. This strategy is associated with durable complete remissions and a low rate of complications and therefore merits further investigation in larger-scale comparative trials.

摘要

供体淋巴细胞输注(DLI)是异基因移植后复发慢性髓性白血病(CML)的一种有效治疗方法,但受到移植物抗宿主病(GVHD)发生的限制。CD8 + T淋巴细胞参与GVHD的发病机制,但对于CML的移植物抗白血病(GVL)效应可能并非必不可少。我们用去除CD8的DLI治疗了26例移植后复发的CML患者。15例早期CML复发患者中有13例(87%)实现了完全细胞遗传学缓解,但11例晚期疾病复发患者中只有1例实现了完全缓解。2例患者(8%)发生了急性GVHD,2例患者(11%)发生了广泛的慢性GVHD。治疗相关死亡率为11.5%。缓解持久;中位随访4.2年(1 - 7.5年),只有1例缓解患者复发(7%)。去除CD8的DLI在无关供体移植和同胞移植后同样有效且安全。DLI时的细胞遗传学克隆进化不能预测治疗失败,除非与疾病加速的血液学标准相关。去除CD8是将移植后复发CML的GVL与GVHD分离的有效方法。该策略与持久的完全缓解和低并发症发生率相关,因此值得在更大规模的比较试验中进一步研究。

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Long-Term follow-up of recipients of CD8-depleted donor lymphocyte infusions for the treatment of chronic myelogenous leukemia relapsing after allogeneic progenitor cell transplantation.接受去除CD8的供体淋巴细胞输注治疗异基因祖细胞移植后复发的慢性粒细胞白血病患者的长期随访
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