同种异体干细胞移植期间的抗生素预防--一项综合性单中心回顾性分析。

IF 3.6 3区 医学 Q2 HEMATOLOGY
Charlotte K F Neuerburg, Friederike Schmitz, Marie-Therese Schmitz, Susanne Rehnelt, Martin Schumacher, Marjio Parčina, Matthias Schmid, Dominik Wolf, Peter Brossart, Tobias A W Holderried
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引用次数: 0

摘要

背景:异基因造血干细胞移植(allo-HSCT)期间预防性使用抗生素仍存在争议。我们移植中心于 2017 年暂停了异基因造血干细胞移植期间的抗生素预防:本研究的主要目的是详细分析异体干细胞移植期间不使用标准抗生素预防对生存率和移植物抗宿主病(GvHD)发展的潜在有利影响,特别是考虑到混杂因素和竞争事件。次要目标是评估在不使用抗生素预防的情况下发生严重感染和移植相关死亡率的风险,详细评估细菌和病毒感染(包括多重耐药病原体)以及两组患者的复发情况。本研究旨在为未来异体 HSCT 抗生素策略的制定提供支持:我们回顾性分析了allo-HSCT期间暂停抗生素预防治疗前(2012年12月至2017年2月)和暂停抗生素预防治疗后(2017年3月至2020年6月)的患者预后。通过病历回顾收集了两组患者(n=221)的相关临床结果参数(使用抗生素预防n=101对未使用抗生素预防n=120)。所有患者均年满 18 岁。采用倾向评分法对可能存在混杂因素的患者特征进行了调整。为了解决竞争事件,我们采用反倾向得分加权多状态建模法分析了中度/重度急性和慢性GvHD、复发和死亡之间的转变:虽然我们观察到未使用抗生素预防的队列结果有改善趋势,但逆倾向得分加权分析并未显示两组患者在总生存期(OS)(p=0.811)或急性并发症(aGvHD)3/4级(p=0.158)和慢性中度/重度并发症(cGvHD)(p=0.686)方面存在显著差异。关于竞争事件的多状态分析显示,在OS方面,不使用抗生素预防与使用抗生素预防的估计概率相当(35.0% [95% CI: 28.2%-42.7%] 对 35.3% [95% CI: 27.8%-41.1%])、3/4 级 aGvHD(7.7% [95% CI:5.9%-12.2%] 对 10.6% [95% CI:7.7%-15.7%])和中度/重度 cGvHD(21.0% [95% CI:17.7%-30.0%] 对 23.8% [95% CI:19.6%-31.4%])的发生率。类似的分析表明,两组患者在复发率、移植相关死亡率、复发相关死亡率或无抗宿主疾病/无复发生存率方面也无明显差异。在未使用抗生素预防的情况下,观察到的严重感染增加并不会导致死亡率显著升高。病毒再激活和多重耐药菌的检测结果相当,但在接受抗生素预防的患者中,艰难梭菌感染的发生率较高:我们的研究支持了之前的报告,即在不使用抗生素预防的情况下,如果怀疑感染,进行密切监测和快速干预,allo-HSCT 并无劣效。不过,在不使用抗生素预防的情况下,治疗效果有改善的趋势,这可能不仅是因为没有使用抗生素预防,还因为近年来该领域取得了更多进展。虽然目前的研究规模太小,无法得出明确的结论,但这些结果强烈要求进一步开展多中心研究,探讨在异体 HSCT 期间省略抗生素预防的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibiotic Prophylaxis During Allogeneic Stem Cell transplantation-A Comprehensive Single Center Retrospective Analysis.

Background: Prophylactic antibiotics are still controversial during allogeneic hematopoietic stem cell transplantation (allo-HSCT). In our transplant center, we suspended antibiotic prophylaxis during allo-HSCT in 2017.

Objective: The main objective of this study was the detailed analysis of the potentially beneficial impact of omittance of standard antibiotic prophylaxis during allo-HSCT in survival and Graft-versus-Host disease (GvHD) development, especially with consideration of confounding factors and competing events. Secondary objectives were the evaluation of the risk of severe infections and transplant-related mortality without antibiotic prophylaxis, the detailed assessment of bacterial and viral infections including multiresistant pathogens as well as occurrence of relapse in both groups. This study aims to support the development of future antibiotic strategies in allo-HSCT.

Study design: We retrospectively analyzed patient outcome in the time periods before (between December 2012 and February 2017) and after suspension (between March 2017 and June 2020) of antibiotic prophylaxis during allo-HSCT. Relevant clinical outcome parameters of the patients (n = 221) were collected by chart-review in the two groups (with antibiotic prophylaxis n = 101 versus without antibiotic prophylaxis n = 120). All patients were 18 years or older. Propensity score methods were used to adjust for potentially confounding patient characteristics. To address competing events, transitions between moderate/severe acute and chronic GvHD, relapse and death were analyzed using an inverse-propensity score weighted multistate modeling approach.

Results: While we observed a trend towards an improved outcome in the cohort without antibiotic prophylaxis, the inverse-propensity-score-weighted analyses did not show significant differences between the two groups in overall survival (OS) (P = .811) or development of acute GvHD (aGvHD) grade 3/4 (P = .158) and chronic moderate/severe GvHD (cGvHD) (P = .686). Multistate analysis respecting competing events revealed comparable estimated probabilities without antibiotic prophylaxis versus with antibiotic prophylaxis in OS (35.0% [95% CI: 28.2%-42.7%] versus 35.3% [95% CI: 27.8%-41.1%]) as well as development of aGvHD grade 3/4 (7.7% [95% CI: 5.9%-12.2%] vs. 10.6% [95% CI: 7.7%-15.7%]) and moderate/severe cGvHD (21.0% [95% CI: 17.7%-30.0%] vs. 23.8% [95% CI: 19.6%-31.4%]). Similar analyses showed also no significant differences in relapse rate, transplant-related mortality, relapse-related mortality, or GvHD-free/relapse-free survival between the two groups. An observed increase in severe infections without antibiotic prophylaxis did not lead to a significantly higher mortality rate. Viral reactivation and detection of multiresistant bacteria were comparable, yet a higher incidence of Clostridioides difficile infections was observed in patients receiving antibiotic prophylaxis.

Conclusion: Our study supports previous reports of noninferiority of allo-HSCT without use of antibiotic prophylaxis with close monitoring and rapid intervention, if infection is suspected. The trend towards improved outcomes without antibiotic prophylaxis, however, might not only be due to the absence of antibiotic prophylaxis but also due to additional progresses in the field over the recent years. While the present study is too small to draw definite conclusions, these results strongly warrant further multicenter studies addressing the potential benefit of omitting antibiotic prophylaxis during allo-HSCT.

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