定义重要:对造血细胞移植后移植物功能不良发生率和结果的多中心调查。

IF 7.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2024-12-17 DOI:10.1002/hem3.70059
Konradin F. Müskens, Winny N. R. Collot-d'Escury, Rana Dandis, Saskia Haitjema, Jürgen Kuball, Moniek A. de Witte, Marc Bierings, Caroline A. Lindemans, Stefan Nierkens, Mirjam E. Belderbos
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引用次数: 0

摘要

尽管同种异体造血细胞移植(HCT)取得了进展,但移植物功能不良(PGF)仍然是一个重要的并发症,具有很高的发病率和死亡率。不同研究报告的发病率和结果不一致,阻碍了对PGF预防和治疗治疗的研究,这可能是由于PGF定义的异质性。为了评估定义异质性的影响,我们进行了一项多中心研究,分析了来自427名儿童和405名成人HCT接受者的35000多个纵向血液计数。基于三种最常见的定义,我们比较了PGF的发病率、危险因素和预后。我们确定了97名儿童和75名成人HCT受者满足至少一种PGF定义。根据所使用的定义,PGF的2年累积发病率差异很大,儿童为6.8%至20%,成人为4.9%至18%。PGF患者的两年死亡率在儿童中为33% - 40%,在成人中为46% - 65%。值得注意的是,仅通过宽松定义确定的PGF患者与移植物功能良好的HCT受体的死亡率相似。在两个队列中,PGF的危险因素在定义上也有所不同,包括较大的受体年龄和脐带血移植。总之,我们的研究表明,PGF定义的差异显著影响报告的发病率、危险因素和结果。这强调了在科学研究、临床实践和移植登记中协调PGF定义的必要性。未来的研究需要使用标准化的、定量的PGF阈值来确定轻度和重度PGF的最佳治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Definitions matter: Multicenter investigation of incidence and outcome of poor graft function after hematopoietic cell transplantation

Definitions matter: Multicenter investigation of incidence and outcome of poor graft function after hematopoietic cell transplantation

Despite advances in allogeneic hematopoietic cell transplantation (HCT), poor graft function (PGF) remains an important complication with substantial morbidity and mortality. The investigation of preventive and therapeutic PGF treatments is hindered by inconsistencies in reported incidence and outcomes across studies, which may be explained by heterogeneity in PGF definition. To assess the impact of definition heterogeneity, we conducted a multicenter study, analyzing over 35.000 longitudinal blood counts from 427 pediatric and 405 adult HCT recipients. We compared the incidence, risk factors, and outcome of PGF, based on the three most common definitions. We identified 97 pediatric and 75 adult HCT recipients fulfilling at least one PGF definition. The 2-year cumulative incidence of PGF varied significantly depending on the definition used, ranging from 6.8% to 20% in children and 4.9% to 18% in adults. Two-year mortality for PGF patients ranged from 33% to 40% in children and 46% to 65% in adults. Notably, PGF patients identified solely by lenient definitions had similar mortality to HCT recipients with good graft function. Risk factors for PGF also varied by definition in both cohorts, and included older recipient age and cord blood transplantation. In conclusion, our study demonstrates that differences in PGF definition significantly impact the reported incidence, risk factors, and outcome. This underscores the need to harmonize PGF definitions across scientific studies, clinical practice, and transplant registries. Future studies, using standardized, quantitative thresholds for PGF, are required to determine optimal treatment strategies for both mild and severe forms of PGF.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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