Ahmad Ali H, Mahadeo Kris M
Pediatric Critical Care Medicine, University of Texas at MD Anderson Cancer Center, Houston, TX, United States.
Pediatric Stem Cell Transplantation and Cellular Therapy and CARTOX Program, University of Texas at MD Anderson Cancer Center, Houston, TX, United States.
Front Oncol. 2021 Feb 24;11:622630. doi: 10.3389/fonc.2021.622630. eCollection 2021.
Hematopoietic Cell Transplantation (HCT) is a potentially curative therapy for children and adolescent/young adults (AYA) with high-risk malignancies as well as some non-malignant genetic diseases. However, HCT may be associated with endotheliopathies and/or organ dysfunction that may progress to pediatric multi-organ dysfunction syndrome (pMODS) and require critical care intervention. Discipline specific scoring systems may be used to characterize individual organ dysfunction, but the extent to which they are used to prospectively monitor HCT patients with mild dysfunction is unknown. Further, separate scoring systems may be used to define risk of mortality and inform prognostication among those who require critical care support. Our understanding of the epidemiology, risk factors, morbidity, mortality, required monitoring, optimal prevention strategies and appropriate management of children undergoing HCT who develop organ dysfunction, endotheliopathies and/or progress to pMODS is poor. Discipline-specific registries and clinical studies have described improving outcomes for children undergoing HCT, including those who require critical care support; however, longitudinal studies/prospective registries that capture common data elements among HCT patients with and without organ dysfunction, endotheliopathies and pMODS are needed to facilitate inter-disciplinary collaboration and optimally characterize the risk profiles, define screening and prophylaxis regimens and mitigate toxicity.
造血细胞移植(HCT)是一种针对患有高危恶性肿瘤以及某些非恶性遗传疾病的儿童和青少年/青年(AYA)的潜在治愈性疗法。然而,HCT可能与内皮病变和/或器官功能障碍相关,这些情况可能进展为小儿多器官功能障碍综合征(pMODS)并需要重症监护干预。特定学科的评分系统可用于描述个体器官功能障碍,但它们用于前瞻性监测轻度功能障碍的HCT患者的程度尚不清楚。此外,可使用单独的评分系统来定义死亡风险,并为需要重症监护支持的患者提供预后信息。我们对接受HCT并出现器官功能障碍、内皮病变和/或进展为pMODS的儿童的流行病学、危险因素、发病率、死亡率、所需监测、最佳预防策略和适当管理的了解不足。特定学科的登记处和临床研究描述了接受HCT的儿童,包括那些需要重症监护支持的儿童的预后改善情况;然而,需要纵向研究/前瞻性登记处以获取有和没有器官功能障碍、内皮病变和pMODS的HCT患者中的常见数据元素,以促进跨学科合作并最佳地描述风险概况、定义筛查和预防方案并减轻毒性。