Ramzan Mohammed, Yadav S P, Zafar Mir Sadaqat Hassan, Dinand Veronique, Sachdeva Anupam
Pediatric Hematology Oncology & BMT Unit, Department of Pediatrics, Sir Ganga Ram Hospital , New Delhi , India.
Pediatr Hematol Oncol. 2014 Feb;31(1):29-38. doi: 10.3109/08880018.2013.807898. Epub 2013 Jun 26.
Outcome data of children with acquired aplastic anemia (AA) are lacking from the developing world. Here, we describe the same from a centre in North India.
Retrospective data regarding medical history, physical examination, complete blood count, bone marrow aspirate, and biopsy were retrieved for all children <18 years, with acquired AA admitted between January 2005 and June 2012. In addition, the outcome data after immunosuppressive therapy (IST) or bone marrow transplant (BMT) was obtained.
A total of 61 children were diagnosed with AA (Inherited-18 and acquired-43). Among 43 children with acquired AA, 3 had nonsevere and 40 had severe. One patient with nonsevere AA died of sepsis and 2 recovered spontaneously. Of the 40 remaining children with severe AA, 10 refused therapy and 3 died due to severe sepsis prior to any therapy. Five underwent upfront matched sibling donor BMT and one post-IST failure. Four year overall survival (OS) and event free survival (EFS) for children undergoing BMT was 100% and 80 ± 17.9, respectively. Out of 22 treated with IST, 20 were evaluable for response. Seventeen received one course and 3 received two course of IST. The overall response to IST was seen in 14/20 (70%). Only two achieved complete response while remaining 12 had partial response. The 4-year estimated OS and EFS for children treated with IST was 74.4 ± 12.1% and 65.6 ± 12.2.
Outcomes for children with AA are encouraging in the developing world although barriers like sepsis and treatment abandonment remain. BMT offers faster and complete recovery.
发展中国家缺乏获得性再生障碍性贫血(AA)患儿的结局数据。在此,我们描述印度北部一个中心的相关情况。
检索了2005年1月至2012年6月期间收治的所有18岁以下获得性AA患儿的病史、体格检查、全血细胞计数、骨髓穿刺及活检的回顾性数据。此外,还获取了免疫抑制治疗(IST)或骨髓移植(BMT)后的结局数据。
共有61名儿童被诊断为AA(遗传性18例,获得性43例)。在43例获得性AA患儿中,3例为非重型,40例为重型。1例非重型AA患儿死于败血症,2例自发缓解。其余40例重型AA患儿中,10例拒绝治疗,3例在接受任何治疗前死于严重败血症。5例接受了直接的同胞全相合供者BMT,1例在IST治疗失败后接受移植。接受BMT的患儿4年总生存率(OS)和无事件生存率(EFS)分别为100%和80±17.9。在22例接受IST治疗的患儿中,20例可评估疗效。17例接受了1个疗程的IST,3例接受了2个疗程的IST。IST的总体有效率为14/20(70%)。仅2例达到完全缓解,其余12例为部分缓解。接受IST治疗的患儿4年估计OS和EFS分别为74.4±12.1%和65.6±12.2。
尽管存在败血症和放弃治疗等障碍,但发展中国家AA患儿的结局令人鼓舞。BMT能带来更快且完全的康复。