Ferrando Giulia, Bagnasco Francesca, Giardino Stefano, Pierri Filomena, Pestarino Sara, Di Marco Eddi, Santaniello Maria, Castagnola Elio, Faraci Maura
Infectious Diseases Unit, Department of Pediatrics, IRCCS Istituto G. Gaslini, 16147 Genova, Italy.
Epidemiology and Biostatistics, Scientific Directorate, IRCCS Istituto G. Gaslini, 16147 Genova, Italy.
Diagnostics (Basel). 2024 Nov 3;14(21):2461. doi: 10.3390/diagnostics14212461.
CMV reactivation represents a frequent complication after HSCT. The aim of this study was to describe the incidence of CMV reactivation in a pediatric HSCT cohort and analyze the potential impact of recipient/donor-related or transplant-related factors on this complication. Furthermore, we analyzed the management of CMV reactivation in order to purpose criteria for pre-emptive therapy.
Allogeneic HSCTs, performed at IRCCS Istituto Gaslini between 2012 and 2022, were included in this analysis. CMV-DNAemia was regularly monitored. Risk stratification was based on donor/recipient serological status and additional potential risk factors were considered: haploidentical transplant; any HSCT subsequent to the first; acute and chronic GvHD; steroids; and other immunosuppressive therapies. We described also the approach for pre-emptive therapy during the period 2012-2019.
A total of 214 allogeneic HSCTs were performed in 189 patients. In total, 100 (46.7%) HSCTs were complicated by at least one reactivation. CMV reactivation was significantly associated with high serological risk and steroid treatment. Pre-emptive therapy was administered in 59/69 (85.5%) HSCTs during 2012-2019. In the presence of predefined risk conditions, therapy was started at a median viremia of 2050 copies/mL. No difference was observed in OS between patients with CMV reactivation versus patients who did not present this complication.
These results suggest the potential effectiveness of the approach used in providing pre-emptive therapy based on viral load monitoring and individualized risk factors.
巨细胞病毒(CMV)再激活是异基因造血干细胞移植(HSCT)后常见的并发症。本研究旨在描述儿童HSCT队列中CMV再激活的发生率,并分析受者/供者相关或移植相关因素对该并发症的潜在影响。此外,我们分析了CMV再激活的管理方法,以制定抢先治疗的标准。
本分析纳入了2012年至2022年在IRCCS加斯利尼研究所进行的异基因HSCT。定期监测CMV血症。风险分层基于供者/受者血清学状态,并考虑其他潜在风险因素:单倍体移植;首次移植后的任何HSCT;急性和慢性移植物抗宿主病(GvHD);类固醇;以及其他免疫抑制治疗。我们还描述了2012 - 2019年期间抢先治疗的方法。
189例患者共进行了214例异基因HSCT。总共100例(46.7%)HSCT至少并发一次再激活。CMV再激活与高血清学风险和类固醇治疗显著相关。2012 - 2019年期间,59/69例(85.5%)HSCT进行了抢先治疗。在存在预定义风险条件时,治疗在病毒血症中位数为2050拷贝/mL时开始。CMV再激活患者与未出现该并发症的患者之间的总生存期(OS)未观察到差异。
这些结果表明,基于病毒载量监测和个体化风险因素的抢先治疗方法具有潜在有效性。