Suppr超能文献

Haploidentical 造血干细胞移植作为儿科重型再生障碍性贫血一线治疗:单中心研究。

Haploidentical hematopoietic stem cell transplantation as a first-line treatment for paediatric severe aplastic anemia: a single-center research.

机构信息

Hematology Center, Beijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Int J Med Sci. 2024 Apr 15;21(6):1027-1036. doi: 10.7150/ijms.94012. eCollection 2024.

Abstract

MRD-HSCT is the first-line therapy for children with SAA, while it is not easy to find a compatible donor due to the Chinese one-child policy. IST has a high recurrence rate, a risk of clonal transformation. Thus, Haplo-HSCT, as a first-line treatment, has gradually attracted clinicians' attention. To evaluate the efficacy of Haplo-HSCT in children with SAA, we performed a retrospective study (2006.06-2021.01) of 210 patients with AA who received HSCT or IST in Beijing Children's Hospital. The OS and FFS rates were analyzed to evaluate the efficacy of Haplo-HSCT and IST. We found that from 2006 to 2021, 3- and 5-year cumulative survival rates were both 85.3% in the first-line Haplo group, 98.1% and 96.8% in the first-line IST group, both 85.7% in the ATG group (P = 0.866), both 100% in the ATG + TPO group (P = 0.016), and 99.1% and 97.2% in the ATG + eltrombopag group (P = 0.056). 3- and 5-year cumulative FFS rates were both 85.3% in the first-line Haplo-HSCT group and 67.5% and 66.2% in the first-line IST group (P = 0.033). Therefore, we believe that Haplo-HSCT can be a first-line treatment for paediatric SAA.

摘要

MRD-HSCT 是 SAA 患儿的一线治疗方法,由于中国的独生子女政策,找到合适的供体并不容易。IST 具有较高的复发率和克隆转化风险。因此,作为一线治疗方法的单倍体 HSCT 逐渐引起了临床医生的关注。为了评估单倍体 HSCT 治疗 SAA 患儿的疗效,我们对 2006 年 6 月至 2021 年 1 月在北京儿童医院接受 HSCT 或 IST 的 210 例 AA 患儿进行了回顾性研究。分析 OS 和 FFS 率,以评估单倍体 HSCT 和 IST 的疗效。我们发现,2006 年至 2021 年,一线单倍体组 3 年和 5 年累计生存率均为 85.3%,一线 IST 组分别为 98.1%和 96.8%,ATG 组为 85.7%(P = 0.866),ATG + TPO 组为 100%(P = 0.016),ATG + eltrombopag 组分别为 99.1%和 97.2%(P = 0.056)。一线单倍体 HSCT 组 3 年和 5 年累计 FFS 率均为 85.3%,一线 IST 组分别为 67.5%和 66.2%(P = 0.033)。因此,我们认为单倍体 HSCT 可作为儿童 SAA 的一线治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b1e/11103391/ddd4d538ebda/ijmsv21p1027g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验