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骨髓衰竭综合征患者接受 HLA 同基因同胞脐血移植的长期结果:来自欧洲血液和骨髓移植学会脐血委员会、cord blood committee 和严重再生障碍性贫血工作组的报告。

Long-Term Outcomes of Cord Blood Transplantation from an HLA-Identical Sibling for Patients with Bone Marrow Failure Syndromes: A Report From Eurocord, Cord Blood Committee and Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation.

机构信息

Hôpital Saint-Louis-Assistance Publique-Hôpitaux de Paris, Paris, France.

Eurocord, Hôpital Saint Louis, Paris, France; Monacord, Monacord, Centre Scientifique de Monaco, Monaco.

出版信息

Biol Blood Marrow Transplant. 2017 Nov;23(11):1939-1948. doi: 10.1016/j.bbmt.2017.08.004. Epub 2017 Aug 7.

DOI:10.1016/j.bbmt.2017.08.004
PMID:
28797779
Abstract

Cord blood transplantation (CBT) from HLA-identical siblings is an attractive option for patients with bone marrow failure (BMF) syndrome because of the low risk of graft-versus-host disease (GVHD) and the absence of risk to the donor. We analyzed outcomes of 117 patients with inherited or acquired BMF syndrome who received CBT from a related HLA-identical donor in European Society for Blood and Marrow Transplantation centers between 1988 and 2014. Ninety-seven patients had inherited and 20 patients acquired BMF syndrome. Eighty-two patients received a single cord blood (CB) unit, whereas 35 patients received a combination of CB and bone marrow cells from the same donor. Median age at CBT was 6.7 years, and median follow-up was 86.7 months. The cumulative incidence function (CIF) of neutrophil recovery was 88.8% (95% CI, 83.1% to 94.9%), 100-day CIF of grades II to IV acute GVHD was 15.2%, and 7-year CIF of chronic GVHD was 14.5%. Overall survival at 7 years was 87.9% (95% CI, 80.8% to 92.6%), 89% for inherited and 81% for acquired BMF syndromes (P = .66). Results of this study are consistent with outcomes of bone marrow transplantation shown by previous series in the same setting and indicate that in pediatric patients with BMF syndrome, CBT from an HLA-identical sibling donor is associated with excellent long-term outcomes and that collection of CB unit at birth of a new sibling is strongly recommended.

摘要

脐血移植(CBT)来自 HLA 完全相同的同胞,是骨髓衰竭(BMF)综合征患者的一个有吸引力的选择,因为移植物抗宿主病(GVHD)的风险低,而且对供体没有风险。我们分析了 1988 年至 2014 年间,欧洲血液和骨髓移植学会中心的 117 例遗传性或获得性 BMF 综合征患者接受相关 HLA 完全相同的供体进行 CBT 的结果。97 例患者患有遗传性 BMF 综合征,20 例患者患有获得性 BMF 综合征。82 例患者接受了单个脐血(CB)单位,而 35 例患者接受了来自同一供体的 CB 和骨髓细胞的组合。CBT 时的中位年龄为 6.7 岁,中位随访时间为 86.7 个月。中性粒细胞恢复的累积发生率(CIF)为 88.8%(95%CI,83.1%至 94.9%),100 天的 II 至 IV 级急性 GVHD 的 CIF 为 15.2%,7 年慢性 GVHD 的 CIF 为 14.5%。7 年的总生存率为 87.9%(95%CI,80.8%至 92.6%),遗传性 BMF 综合征为 89%,获得性 BMF 综合征为 81%(P=0.66)。本研究结果与同一环境下先前系列的骨髓移植结果一致,表明在儿科 BMF 综合征患者中,来自 HLA 完全相同的同胞供体的 CBT 与极好的长期结果相关,强烈建议在新的同胞出生时收集 CB 单位。

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