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匹配同胞供者造血干细胞移植与镰状细胞贫血儿童经颅多普勒血流速度的相关性。

Association of Matched Sibling Donor Hematopoietic Stem Cell Transplantation With Transcranial Doppler Velocities in Children With Sickle Cell Anemia.

机构信息

Referral Center for Sickle Cell Disease, Department of Pediatrics, Intercommunal Créteil Hospital, University Paris-Est, Créteil, France.

Referral Center for Sickle Cell Disease, Medical Imaging Department, Intercommunal Créteil Hospital, Créteil, France.

出版信息

JAMA. 2019 Jan 22;321(3):266-276. doi: 10.1001/jama.2018.20059.


DOI:10.1001/jama.2018.20059
PMID:30667500
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6439675/
Abstract

IMPORTANCE: In children with sickle cell anemia (SCA), high transcranial Doppler (TCD) velocities are associated with stroke risk, which is reduced by chronic transfusion. Whether matched sibling donor hematopoietic stem cell transplantation (MSD-HSCT) can reduce velocities in patients with SCA is unknown. OBJECTIVE: To determine the association of MSD-HSCT with TCD velocities as a surrogate for the occurrence of ischemic stroke in children with SCA. DESIGN, SETTING, AND PARTICIPANTS: Nonrandomized controlled intervention study conducted at 9 French centers. Patients with SCA were enrolled between December 2010 and June 2013, with 3-year follow-up ending in January 2017. Children with SCA were eligible if younger than 15 years, required chronic transfusions for persistently elevated TCD velocities, and had at least 1 sibling without SCA from the same 2 parents. Families agreed to HLA antigen typing and transplantation if a matched sibling donor was identified or to standard care in the absence of a matched sibling donor. EXPOSURES: MSD-HSCT (n = 32), compared with standard care (n = 35) (transfusions for ≥1 year with potential switch to hydroxyurea thereafter), using propensity score matching. MAIN OUTCOMES AND MEASURES: The primary outcome was the highest time-averaged mean of maximum velocities in 8 cerebral arteries, measured by TCD (TCD velocity) at 1 year. Twenty-five of 29 secondary outcomes were analyzed, including the highest TCD velocity at 3 years and normalization of velocities (<170 cm/s) and ferritin levels at 1 and 3 years. RESULTS: Sixty-seven children with SCA (median age, 7.6 years; 35 girls [52%]) were enrolled (7 with stroke history). In the matched sample, highest TCD velocities at 1 year were significantly lower on average in the transplantation group (129.6 cm/s) vs the standard care group (170.4 cm/s; difference, -40.8 cm/s [95% CI, -62.9 to -18.6]; P < .001). Of the 25 analyzed secondary end points, 4 showed significant differences, including the highest TCD velocity at 3 years (112.4 cm/s in the transplantation group vs 156.7 cm/s in the standard care group; difference, -44.3 [95% CI, -71.9 to -21.1]; P = .001); normalization rate at 1 year (80.0% in the transplantation group vs 48.0% in the standard care group; difference, 32.0% [95% CI, 0.2% to 58.6%]; P = .045); and ferritin levels at 1 year (905 ng/mL in the transplantation group vs 2529 ng/mL in the standard care group; difference, -1624 [95% CI, -2370 to -879]; P < .001) and 3 years (382 ng/mL in the transplantation group vs 2170 ng/mL in the standard care group; difference, -1788 [95% CI, -2570 to -1006]; P < .001). CONCLUSIONS AND RELEVANCE: Among children with SCA requiring chronic transfusion because of persistently elevated TCD velocities, MSD-HSCT was significantly associated with lower TCD velocities at 1 year compared with standard care. Further research is warranted to assess the effects of MSD-HSCT on clinical outcomes and over longer follow-up. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01340404.

摘要

重要性:在患有镰状细胞贫血(SCA)的儿童中,高经颅多普勒(TCD)速度与中风风险相关,慢性输血可降低中风风险。骨髓干细胞移植(MSD-HSCT)是否可以降低 SCA 患者的 TCD 速度尚不清楚。

目的:确定 MSD-HSCT 与 TCD 速度的关联,作为 SCA 患儿发生缺血性中风的替代指标。

设计、地点和参与者:在法国 9 个中心进行的非随机对照干预研究。2010 年 12 月至 2013 年 6 月期间招募 SCA 患儿,3 年随访于 2017 年 1 月结束。如果 TCD 速度持续升高需要长期输血且至少有 1 位来自同一对父母的无 SCA 同胞,则符合入组条件。如果发现匹配的同胞供体,患儿及其家属同意 HLA 抗原分型和移植,否则在无匹配同胞供体的情况下接受标准治疗。

暴露因素:MSD-HSCT(n=32),与标准治疗(n=35)相比,后者在输血至少 1 年后(之后可能转为羟基脲),采用倾向评分匹配。

主要结局和测量指标:主要结局是通过 TCD(TCD 速度)在 1 年时测量的 8 条脑动脉的最高时间平均最大速度。25 个次要结局中有 25 个被分析,包括 3 年时的最高 TCD 速度以及 1 年和 3 年时 TCD 速度和铁蛋白水平的正常化。

结果:共有 67 名 SCA 患儿(中位年龄 7.6 岁;35 名女孩[52%])入组(7 名有中风史)。在匹配样本中,移植组 TCD 速度在 1 年时的平均速度明显低于标准治疗组(129.6 cm/s 比 170.4 cm/s;差值,-40.8 cm/s [95%CI,-62.9 至-18.6];P<.001)。在 25 个分析的次要终点中,有 4 个有显著差异,包括 3 年时的最高 TCD 速度(移植组 112.4 cm/s,标准治疗组 156.7 cm/s;差值,-44.3 [95%CI,-71.9 至-21.1];P=.001);1 年时的正常化率(移植组 80.0%,标准治疗组 48.0%;差值,32.0% [95%CI,0.2% 至 58.6%];P=.045);以及 1 年和 3 年时的铁蛋白水平(移植组 905 ng/mL,标准治疗组 2529 ng/mL;差值,-1624 [95%CI,-2370 至-879];P<.001)。

结论和相关性:在因 TCD 速度持续升高而需要长期输血的 SCA 患儿中,与标准治疗相比,MSD-HSCT 与 1 年时的 TCD 速度显著降低相关。需要进一步研究以评估 MSD-HSCT 对临床结局和更长随访时间的影响。

试验注册:ClinicalTrials.gov 标识符:NCT01340404。

相似文献

[1]
Association of Matched Sibling Donor Hematopoietic Stem Cell Transplantation With Transcranial Doppler Velocities in Children With Sickle Cell Anemia.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[10]
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[7]
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[8]
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[9]
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本文引用的文献

[1]
Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia.

Adv Exp Med Biol. 2017

[2]
Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404).

Contemp Clin Trials. 2017-11

[3]
Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities.

Blood. 2016-2-5

[4]
Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial.

Lancet. 2016-2-13

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What is the best cryopreservation protocol for human testicular tissue banking?

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Pharmacoepidemiol Drug Saf. 2012-10-16

[10]
Health-related quality of life in sickle cell disease: past, present, and future.

Pediatr Blood Cancer. 2012-4-22

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