Department of Pediatric Hematology and Oncology, Nicolaus Copernicus University Torun, Collegium Medicum, Bydgoszcz, Poland.
Department of Microbiology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Front Immunol. 2024 Jul 11;15:1427637. doi: 10.3389/fimmu.2024.1427637. eCollection 2024.
Children undergoing allo-HCT are at high risk of EBV-related complications. The objective of the study was to analyze the impact of prophylactic post-transplant rituximab on EBV infection and EBV-PTLD in children after allo-HCT, to determine the risk factors for the development of EBV infection and EBV-PTLD and to determine their outcomes. Additionally, the impact of EBV-driven complications on transplant outcomes was analyzed.
Single center retrospective analysis of EBV-related complications in pediatric population undergoing allo-HCT, based on strategy of prophylaxis with rituximab. Overall 276 consecutive children, including 122 on prophylaxis, were analyzed for EBV-driven complications and transplant outcomes.
Prophylaxis with rituximab resulted in significant reduction of EBV infection (from 35.1% to 20.5%; HR=2.7; p<0.0001), and EBV-PTLD (from 13.0% to 3.3%; HR=0.23; p=0.0045). A trend for improved survival was also observed (HR=0.66; p=0.068), while non-relapse mortality was comparable in both cohorts. The peak value of viral load was a risk factor in the development of EBV-PTLD: 10-fold higher peak viral load in comparison to the baseline 10 copies/mL, caused a 3-fold (HR=3.36; p<0.001) increase in the risk of EBV-PTLD. Rituximab treatment was effective as a preemptive therapy in 91.1%, and in 70.9% in EBV-PTLD. Patients who developed PTLD had dismal 5-year overall survival (29% vs 60%; p<0.001), and an increased risk of relapse (72% vs 35%; p=0.024).
Rituximab for prophylaxis of EBV infection and EBV-PTLD was highly effective in pediatric population. Treatment of EBV-PTLD was successful in 70%, however the occurrence of EBV-PTLD was associated with an increased risk of relapse of primary malignant disease.
接受异基因造血干细胞移植(allo-HCT)的儿童存在 EBV 相关并发症的高风险。本研究的目的是分析移植后预防性利妥昔单抗对 allo-HCT 后儿童 EBV 感染和 EBV-PTLD 的影响,确定 EBV 感染和 EBV-PTLD 发展的危险因素,并确定其结果。此外,还分析了 EBV 驱动的并发症对移植结果的影响。
对接受 allo-HCT 的儿科人群进行基于利妥昔单抗预防策略的 EBV 相关并发症的单中心回顾性分析。共分析了 276 例连续儿童患者,其中 122 例接受了预防治疗,以评估 EBV 驱动的并发症和移植结果。
利妥昔单抗预防可显著降低 EBV 感染(从 35.1%降至 20.5%;HR=2.7;p<0.0001)和 EBV-PTLD(从 13.0%降至 3.3%;HR=0.23;p=0.0045)的发生率。也观察到生存改善的趋势(HR=0.66;p=0.068),而两组的非复发死亡率相当。病毒载量峰值是 EBV-PTLD 发展的危险因素:与基线 10 拷贝/ml 相比,病毒载量峰值增加 10 倍,导致 EBV-PTLD 的风险增加 3 倍(HR=3.36;p<0.001)。利妥昔单抗治疗作为抢先治疗在 91.1%的患者中有效,在 EBV-PTLD 中有效率为 70.9%。发生 PTLD 的患者 5 年总生存率极差(29%比 60%;p<0.001),复发风险增加(72%比 35%;p=0.024)。
利妥昔单抗预防 EBV 感染和 EBV-PTLD 在儿科人群中非常有效。EBV-PTLD 的治疗成功率为 70%,但 EBV-PTLD 的发生与原发性恶性疾病复发风险增加有关。