Szmit Zofia, Frączkiewicz Jowita, Salamonowicz-Bodzioch Małgorzata, Król Anna, Ussowicz Marek, Mielcarek-Siedziuk Monika, Liszka Karolina, Marschollek Paweł, Gorczyńska Ewa, Kałwak Krzysztof
Department of Pediatric Hematology/Oncology and BMT, Wroclaw Medical University, Supraregional Center of Pediatric Oncology "Cape of Hope", 50-556 Wrocław, Poland.
J Clin Med. 2022 Sep 1;11(17):5187. doi: 10.3390/jcm11175187.
Hematopoietic stem cell transplantation (HSCT) is a curative therapy for an increasing number of nonmalignant indications. Its use is restricted by severe transplant-related complications, including CMV infection; despite various prophylactic and therapeutic strategies, CMV reactivation has remarkable morbidity and mortality. The analysis included 94 children with nonmalignant disorder who underwent allogeneic HSCT in the Department of Pediatric Hematology, Oncology, and Bone Marrow Transplantation in Wrocław during years 2016-2020. Twenty-seven (29%) children presented with CMV infection, including ten (10/27; 37%) with high level CMV viremia (10,000 copies/mL). Six patients experienced subsequent CMV reactivation. The first-line ganciclovir-based (GCV) treatment was insufficient in 40% (11/27) of children. Overall survival (OS) was significantly lower in children with high CMV viremia compared to those with low levels/no CMV [1yrOS High CMV = 0.80 (95% CI 0.41-0.95) vs. 1yrOS others = 0.96 (95% CI 0.89-0.99)]. Similarly, patients with resistant and recurrent infections had greater risk of death. CMV reactivation at any level relevantly prolonged the hospital stay. CMV reactivation with high viremia load and resistant/recurrent CMV infections lead to a significant decrease in OS in children with nonmalignant disorders treated with HSCT. Our data proves there is an urgent need to introduce an effective anti-CMV prophylaxis in this cohort of patients.
造血干细胞移植(HSCT)是一种针对越来越多非恶性疾病的治愈性疗法。其应用受到包括巨细胞病毒(CMV)感染在内的严重移植相关并发症的限制;尽管有各种预防和治疗策略,但CMV再激活仍具有显著的发病率和死亡率。该分析纳入了2016年至2020年期间在弗罗茨瓦夫儿科血液学、肿瘤学和骨髓移植科接受异基因HSCT的94例非恶性疾病患儿。27例(29%)患儿出现CMV感染,其中10例(10/27;37%)出现高水平CMV病毒血症(≥10,000拷贝/mL)。6例患者随后发生CMV再激活。40%(11/27)的患儿基于更昔洛韦(GCV)的一线治疗效果不佳。与低水平/无CMV的患儿相比,CMV病毒血症高的患儿总体生存率(OS)显著更低[1年OS高CMV = 0.80(95%CI 0.41 - 0.95)vs. 1年OS其他 = 0.96(95%CI 0.89 - 0.99)]。同样,耐药和反复感染的患者死亡风险更高。任何水平的CMV再激活均显著延长住院时间。高病毒载量的CMV再激活以及耐药/反复的CMV感染导致接受HSCT治疗的非恶性疾病患儿的OS显著降低。我们的数据证明,迫切需要在这组患者中引入有效的抗CMV预防措施。