Departments of (1)Microbiology and Immunology and (2)Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
Departments of (1)Microbiology and Immunology and (2)Pediatrics, Medical University of South Carolina, Charleston, South Carolina.
Transplant Cell Ther. 2022 Oct;28(10):657-666. doi: 10.1016/j.jtct.2022.07.008. Epub 2022 Jul 11.
Hematopoietic cell transplantation (HCT) is a potentially curative treatment for many hematologic and nonhematologic disorders. Graft-versus-host-disease (GVHD) in its acute or chronic form remains the most important nonrelapse post-HCT complication. Biomarkers offer objective, unbiased information on systemic disorders, and significant attention has focused on identifying biomarkers for GVHD. Ideally, a GVHD biomarker is actionable, with the results of biomarker testing used to guide clinical management of disease and clinical trial design. Although many GVHD biomarkers have been identified, none have been properly qualified for clinical use. The National Institutes of Health (NIH) and Food and Drug Administration (FDA) have provided biomarker subtype definitions; however, confusion remains about the proper definition and application of these subtypes in the HCT field. The 2014 NIH consensus development project provided a framework for the development of biomarkers for clinical practice. This review aims to clarify the biomarker subtype definitions and reemphasize the developmental framework. Armed with this knowledge, clinicians can properly translate GVHD biomarkers for clinical use.
造血细胞移植(HCT)是许多血液系统和非血液系统疾病的潜在治愈性治疗方法。移植物抗宿主病(GVHD)无论是急性还是慢性,仍然是移植后最重要的非复发并发症。生物标志物提供了有关全身疾病的客观、无偏倚的信息,因此人们高度关注识别 GVHD 的生物标志物。理想情况下,GVHD 生物标志物是可操作的,生物标志物检测的结果可用于指导疾病的临床管理和临床试验设计。尽管已经确定了许多 GVHD 生物标志物,但没有一种被适当确认为临床应用。美国国立卫生研究院(NIH)和食品和药物管理局(FDA)已经提供了生物标志物亚型定义;然而,在 HCT 领域,这些亚型的正确定义和应用仍然存在混淆。2014 年 NIH 共识发展项目为临床实践中的生物标志物开发提供了框架。本综述旨在澄清生物标志物亚型定义,并再次强调发展框架。有了这些知识,临床医生就可以正确地将 GVHD 生物标志物转化为临床应用。