Neuerburg Charlotte K F, Schmitz Friederike, Schmitz Marie-Therese, Rehnelt Susanne, Schumacher Martin, Parčina Marjio, Schmid Matthias, Wolf Dominik, Brossart Peter, Holderried Tobias A W
Department of Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, Bonn, Germany; Center for Integrated Oncology (CIO) ABCD, Aachen Bonn Cologne Düsseldorf, Germany.
Institute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Bonn, Germany.
Transplant Cell Ther. 2024 Dec;30(12):1195.e1-1195.e13. doi: 10.1016/j.jtct.2024.09.011. Epub 2024 Sep 17.
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.
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.
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.
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.
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.
在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。在我们的移植中心,2017年我们在allo-HSCT期间暂停了抗生素预防。
本研究的主要目的是详细分析在allo-HSCT期间省略标准抗生素预防对生存和移植物抗宿主病(GvHD)发生的潜在有益影响,尤其要考虑混杂因素和竞争事件。次要目的是评估无抗生素预防时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的复发情况。本研究旨在支持未来allo-HSCT抗生素策略的制定。
我们回顾性分析了allo-HSCT期间抗生素预防暂停前(2012年12月至2017年2月)和暂停后(2017年3月至2020年6月)时间段内患者的结局。通过病历审查收集两组(n = 221)患者的相关临床结局参数(有抗生素预防n = 101,无抗生素预防n = 120)。所有患者年龄均在18岁及以上。采用倾向评分方法调整潜在的混杂患者特征。为处理竞争事件,使用逆倾向评分加权多状态建模方法分析中度/重度急性和慢性GvHD、复发和死亡之间的转换。
虽然我们观察到无抗生素预防队列中有结局改善的趋势,但逆倾向评分加权分析显示两组在总生存期(OS)(P = 0.811)、3/4级急性GvHD(aGvHD)(P = 0.158)和慢性中度/重度GvHD(cGvHD)(P = 0.686)的发生方面无显著差异。考虑竞争事件的多状态分析显示,无抗生素预防与有抗生素预防相比,OS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的发生情况也相当(7.7% [95% CI:5.9%-12.2%] 对10.6% [95% CI:7.7%-15.7%]),中度/重度cGvHD的情况同样如此(21.0% [95% CI:17.7%-30.0%] 对23.8% [95% CI:19.6%-31.4%])。类似分析还显示两组在复发率、移植相关死亡率、复发相关死亡率或无GvHD/无复发生存方面无显著差异。观察到无抗生素预防时严重感染增加,但未导致显著更高的死亡率。病毒再激活和多重耐药菌的检测相当,但在接受抗生素预防的患者中观察到艰难梭菌感染的发生率更高。
我们的研究支持先前关于在密切监测和怀疑感染时进行快速干预的情况下,不使用抗生素预防的allo-HSCT非劣效性的报道。然而,无抗生素预防时结局改善的趋势可能不仅归因于无抗生素预防,还归因于近年来该领域的其他进展。虽然本研究规模太小无法得出明确结论,但这些结果强烈支持进一步开展多中心研究,以探讨在allo-HSCT期间省略抗生素预防的潜在益处。