Second Allogeneic Hematopoietic Cell Transplantation Following Graft Failure in Children.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Eun Sang Yi, Hee Young Ju, Ji Won Lee, Ki Woong Sung, Jin Hur, Keon Hee Yoo
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Abstract

Background: Graft failure (GF) is a major complication of allogeneic hematopoietic cell transplantation (allo-HCT). Secondary transplantation has been recognized as a potential curative intervention.

Methods: This study aimed to investigate the characteristics and outcomes of salvage transplantation by analyzing the patients who underwent a second HCT for GF following the initial allo-HCT between 1998 and 2020.

Results: Overall, 23 recipients were identified, including 14 and 9 individuals with primary and secondary GF, respectively. Nine recipients underwent a second transplant from the same donor. Familial mismatched donors predominated in the second HCT (86.9%), with reduced-intensity conditioning as the prevailing approach (60.9%). Neutrophil engraftment occurred in 17 patients (73.9%) following the second HCT at a median of 17 days (range: 9-58 days) post-transplantation. However, secondary GF subsequently occurred in 5 patients, and successful engraftment following salvage transplantation was achieved in 12 (52.2%) patients. In the entire study population, the estimated 5-year probability of overall survival (OS) and treatment-related mortality (TRM) were 30.4% and 58.5%, respectively. Among patients who achieved successful engraftment following a second transplantation, the OS and TRM rates were 41.7% and 33.3%, respectively, indicating a trend toward better OS and significantly lower TRM compared to those with GF. Notably, 17 patients died, with infection being the most common cause (n = 12), irrespective of the engraftment status.

Conclusion: A successful engraftment following a second allo-HCT reduced the TRM; however, the OS remained suboptimal. The effective control of infectious diseases remains crucial for patients with GF, regardless of the engraftment status following salvage transplantation.

儿童移植失败后的第二次异体造血细胞移植。
背景:移植物衰竭(GF)是同种异体造血细胞移植(allo-HCT)的主要并发症。二次移植已被认为是一种潜在的治疗干预手段。方法:本研究旨在通过分析1998年至2020年间在首次同种异体造血干细胞移植后接受第二次造血干细胞移植的患者,来调查补救性移植的特点和结果。结果:总共确定了23例受者,包括14例原发性GF和9例继发性GF。9名受赠者接受了来自同一供者的第二次移植。家族性错配供体在第二次HCT中占主导地位(86.9%),低强度调节是主要方法(60.9%)。17例患者(73.9%)在移植后中位17天(范围:9-58天)进行第二次HCT后出现中性粒细胞植入。然而,5例患者随后发生继发性GF, 12例(52.2%)患者在补救性移植后成功植入。在整个研究人群中,估计的5年总生存率(OS)和治疗相关死亡率(TRM)分别为30.4%和58.5%。在第二次移植后成功植入的患者中,OS和TRM率分别为41.7%和33.3%,表明与GF相比,有更好的OS和显著降低TRM的趋势。值得注意的是,17例患者死亡,感染是最常见的原因(n = 12),与植入状态无关。结论:在第二次同种异体ct后成功植入降低了TRM;然而,操作系统仍然不是最优的。对GF患者来说,有效控制感染性疾病仍然是至关重要的,无论补救性移植后的移植状态如何。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Korean Medical Science
Journal of Korean Medical Science 医学-医学:内科
CiteScore
7.80
自引率
8.90%
发文量
320
审稿时长
3-6 weeks
期刊介绍: The Journal of Korean Medical Science (JKMS) is an international, peer-reviewed Open Access journal of medicine published weekly in English. The Journal’s publisher is the Korean Academy of Medical Sciences (KAMS), Korean Medical Association (KMA). JKMS aims to publish evidence-based, scientific research articles from various disciplines of the medical sciences. The Journal welcomes articles of general interest to medical researchers especially when they contain original information. Articles on the clinical evaluation of drugs and other therapies, epidemiologic studies of the general population, studies on pathogenic organisms and toxic materials, and the toxicities and adverse effects of therapeutics are welcome.
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