再生障碍性贫血
救世主兄弟
造血干细胞移植
医学
单中心
造血
移植
造血细胞
中心(范畴论)
干细胞
贫血
外科
内科学
生物
骨髓
化学
遗传学
结晶学
作者
Meng Yuan,Chenguang Jia,Jie Ma,Man Zhang,Guanghua Zhu,Bin Wang,Jie Zheng,Maoquan Qin,Runhui Wu,Sidan Li
摘要
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.
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