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儿童获得性再生障碍性贫血的结局:发展中世界的经验

Outcome of pediatric acquired aplastic anemia: a developing world experience.

作者信息

Ramzan Mohammed, Yadav S P, Zafar Mir Sadaqat Hassan, Dinand Veronique, Sachdeva Anupam

机构信息

Pediatric Hematology Oncology & BMT Unit, Department of Pediatrics, Sir Ganga Ram Hospital , New Delhi , India.

出版信息

Pediatr Hematol Oncol. 2014 Feb;31(1):29-38. doi: 10.3109/08880018.2013.807898. Epub 2013 Jun 26.

Abstract

INTRODUCTION

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

引言

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。

方法

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。

结果

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。

结论

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。

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