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造血干细胞移植治疗巴西原发性免疫缺陷:发展中国家治疗罕见病的挑战。

Transplantation of Hematopoietic Stem Cells for Primary Immunodeficiencies in Brazil: Challenges in Treating Rare Diseases in Developing Countries.

机构信息

Instituto da Criança - Hospital das Clínicas da Universidade de São Paulo, São Paulo, Brazil.

Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.

出版信息

J Clin Immunol. 2018 Nov;38(8):917-926. doi: 10.1007/s10875-018-0564-1. Epub 2018 Nov 24.

DOI:10.1007/s10875-018-0564-1
PMID:30470982
Abstract

The results of hematopoietic stem cell transplant (HSCT) for primary immunodeficiency diseases (PID) have been improving over time. Unfortunately, developing countries do not experience the same results. This first report of Brazilian experience of HSCT for PID describes the development and results in the field. We included data from transplants in 221 patients, performed at 11 centers which participated in the Brazilian collaborative group, from July 1990 to December 2015. The majority of transplants were concentrated in one center (n = 123). The median age at HSCT was 22 months, and the most common diseases were severe combined immunodeficiency (SCID) (n = 67) and Wiskott-Aldrich syndrome (WAS) (n = 67). Only 15 patients received unconditioned transplants. Cumulative incidence of GVHD grades II to IV was 23%, and GVHD grades III to IV was 10%. The 5-year overall survival was 71.6%. WAS patients had better survival compared to other diseases. Most deaths (n = 53) occurred in the first year after transplantation mainly due to infection (55%) and GVHD (13%). Although transplant for PID patients in Brazil has evolved since its beginning, we still face some challenges like delayed diagnosis and referral, severe infections before transplant, a limited number of transplant centers with expertise, and resources for more advanced techniques. Measures like newborn screening for SCID may hasten the diagnosis and ameliorate patients' conditions at the moment of transplant.

摘要

造血干细胞移植(HSCT)治疗原发性免疫缺陷病(PID)的疗效一直在改善。不幸的是,发展中国家并未取得同样的效果。本报告首次介绍了巴西在 PID 领域开展 HSCT 的经验和结果。我们纳入了 1990 年 7 月至 2015 年 12 月期间,在参与巴西协作组的 11 个中心接受移植的 221 例患者的数据。大多数移植都集中在一个中心(n=123)。HSCT 的中位年龄为 22 个月,最常见的疾病是严重联合免疫缺陷(SCID)(n=67)和 Wiskott-Aldrich 综合征(WAS)(n=67)。仅有 15 例患者接受了非条件性移植。Ⅱ至Ⅳ级移植物抗宿主病(GVHD)的累积发生率为 23%,Ⅲ至Ⅳ级 GVHD 的发生率为 10%。5 年总生存率为 71.6%。与其他疾病相比,WAS 患者的生存率更高。大多数死亡(n=53)发生在移植后 1 年内,主要原因是感染(55%)和 GVHD(13%)。尽管巴西 PID 患者的移植自开展以来已有进展,但我们仍面临一些挑战,如诊断和转诊延迟、移植前严重感染、具有专业知识的移植中心数量有限以及先进技术资源不足。SCID 的新生儿筛查等措施可能会加速诊断,并改善移植时患者的病情。

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