Suppr超能文献

同种异体造血干细胞移植治疗儿童急性髓系白血病:来自印度一家三级护理中心的经验教训。

Allogeneic hematopoietic stem cell transplant in pediatric acute myeloid leukemia: Lessons learnt from a tertiary care center in India.

机构信息

Department of Medical Oncology, Dr. BRAIRCH, AIIMS, New Delhi, India.

Unit of Laboratory Oncology, Dr. BRAIRCH, AIIMS, New Delhi, India.

出版信息

Pediatr Transplant. 2021 May;25(3):e13918. doi: 10.1111/petr.13918. Epub 2020 Nov 3.

Abstract

There is paucity of data on outcomes of MSD-HSCT in children with relapsed or high-risk AML from developing countries, which have unique challenges including adverse host factors and resource constraints. We retrospectively reviewed records of children (age ≤ 18 years) who underwent MSD-HSCT for AML at our center from 2009 to 2019 to evaluate clinical outcome and its predictors using Cox proportional hazards model. There were 46 children (36 boys and 10 girls) with mean age 10.7 ± 4.8 years. Indication for HSCT was relapsed AML in CR2 (n = 37), primary refractory (n = 3), or relapsed refractory disease (n = 3); high-risk (n = 1) or secondary (n = 2) AML in CR1. Five-year EFS and OS were 33.3 ± 7.2% and 36.3 ± 7.6%, respectively. On multivariate analysis, CR1 duration less than 12 months, presence of active disease at transplant, and use of bone marrow stem cell graft were associated with poorer EFS and OS. There was one (2.2%) TRM, while disease relapse occurred in 20/40 patients who underwent HSCT in remission. Though the 5-year EFS and OS were inferior to results reported from high-income countries, relapse (and not TRM) was the major cause of treatment failure. A well-sustained CR1, achievement of disease remission, and use of peripheral blood allograft seem imperative to a successful transplant. Targeted therapy along with HSCT may be the option for those with early relapse.

摘要

在发展中国家,由于宿主因素不利和资源有限等独特挑战,有关儿童复发或高危急性髓系白血病(AML)接受骨髓移植(MSD-HSCT)后结局的数据十分匮乏。我们回顾性分析了 2009 年至 2019 年在我中心接受 MSD-HSCT 治疗 AML 的儿童(年龄≤18 岁)的病历记录,采用 Cox 比例风险模型评估临床结局及其预测因素。共有 46 例儿童(36 名男孩和 10 名女孩),平均年龄为 10.7±4.8 岁。HSCT 的适应证为完全缓解 2 期(CR2)复发(n=37)、原发耐药(n=3)或复发耐药疾病(n=3);CR1 期的高危(n=1)或继发性(n=2)AML。5 年无事件生存率(EFS)和总生存率(OS)分别为 33.3±7.2%和 36.3±7.6%。多变量分析显示,CR1 期持续时间<12 个月、移植时存在活动性疾病以及使用骨髓干细胞移植物与较差的 EFS 和 OS 相关。有 1 例(2.2%)发生移植相关死亡(TRM),而在缓解期接受 HSCT 的 40 例患者中,有 20 例发生疾病复发。尽管 5 年 EFS 和 OS 不如高收入国家报道的结果,但复发(而非 TRM)是治疗失败的主要原因。维持良好的 CR1、达到疾病缓解以及使用外周血移植物似乎是移植成功的关键。针对早期复发的患者,靶向治疗联合 HSCT 可能是一种选择。

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