共 50 条
Monitoring and Management of Cytomegalovirus Reactivations After Allogeneic Hematopoietic Stem Cell Transplantation in Children: Experience from a Single Pediatric Center
被引:0
|作者:
Ferrando, Giulia
[1
]
Bagnasco, Francesca
[2
]
Giardino, Stefano
[3
]
Pierri, Filomena
[3
]
Pestarino, Sara
[3
]
Di Marco, Eddi
[4
]
Santaniello, Maria
[1
]
Castagnola, Elio
[1
]
Faraci, Maura
[3
]
机构:
[1] IRCCS Ist G Gaslini, Dept Pediat, Infect Dis Unit, I-16147 Genoa, Italy
[2] IRCCS Ist G Gaslini, Epidemiol & Biostat, Sci Directorate, I-16147 Genoa, Italy
[3] IRCCS Ist G Gaslini, Dept Hemato Oncol, Hematopoiet Stem Cell Transplant Unit, I-16147 Genoa, Italy
[4] IRCCS Ist G Gaslini, Mol Med Lab, I-16147 Genoa, Italy
来源:
关键词:
hematopoietic stem cell transplantation;
viral infection;
cytomegalovirus;
pre-emptive therapy;
VERSUS-HOST-DISEASE;
INFECTION;
THERAPY;
SOCIETY;
RISK;
D O I:
10.3390/diagnostics14212461
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: 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. Methods: 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. Results: 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. Conclusions: These results suggest the potential effectiveness of the approach used in providing pre-emptive therapy based on viral load monitoring and individualized risk factors.
引用
收藏
页数:11
相关论文