Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Division of Pediatric Hematology/Oncology, Dpeartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
Transplant Cell Ther. 2021 Aug;27(8):632-641. doi: 10.1016/j.jtct.2021.03.029. Epub 2021 Apr 6.
Chronic graft-versus-host disease (GVHD) commonly occurs after allogeneic hematopoietic cell transplantation (HCT) despite standard prophylactic immune suppression. Intensified universal prophylaxis approaches are effective but risk possible overtreatment and may interfere with the graft-versus-malignancy immune response. Here we summarize conceptual and practical considerations regarding preemptive therapy of chronic GVHD, namely interventions applied after HCT based on evidence that the risk of developing chronic GVHD is higher than previously appreciated. This risk may be anticipated by clinical factors or risk assignment biomarkers or may be indicated by early signs and symptoms of chronic GVHD that do not fully meet National Institutes of Health diagnostic criteria. However, truly preemptive, individualized, and targeted chronic GVHD therapies currently do not exist. In this report, we (1) review current knowledge regarding clinical risk factors for chronic GVHD, (2) review what is known about chronic GVHD risk assignment biomarkers, (3) examine how chronic GVHD pathogenesis intersects with available targeted therapeutic agents, and (4) summarize considerations for preemptive therapy for chronic GVHD, emphasizing trial development, including trial design and statistical considerations. We conclude that robust risk assignment models that accurately predict chronic GVHD after HCT and early-phase preemptive therapy trials represent the most urgent priorities for advancing this novel area of research.
慢性移植物抗宿主病(GVHD)在异基因造血细胞移植(HCT)后很常见,尽管采用了标准的预防免疫抑制。强化的通用预防方法是有效的,但存在过度治疗的风险,并且可能会干扰移植物抗恶性肿瘤的免疫反应。在这里,我们总结了关于慢性 GVHD 抢先治疗的概念和实际考虑因素,即基于以下证据在 HCT 后应用的干预措施:发生慢性 GVHD 的风险高于先前的认识。这种风险可以通过临床因素或风险分配生物标志物来预测,也可以通过尚未完全符合美国国立卫生研究院诊断标准的慢性 GVHD 的早期迹象和症状来提示。然而,目前确实不存在真正的、个体化的、有针对性的慢性 GVHD 治疗方法。在本报告中,我们(1)回顾了关于慢性 GVHD 的临床危险因素的现有知识,(2)回顾了关于慢性 GVHD 风险分配生物标志物的了解,(3)研究了慢性 GVHD 的发病机制如何与现有靶向治疗药物交叉,以及(4)总结了慢性 GVHD 抢先治疗的考虑因素,重点介绍了试验开发,包括试验设计和统计考虑。我们得出的结论是,准确预测 HCT 后慢性 GVHD 的强大风险分配模型和早期抢先治疗试验代表了推进这一新兴研究领域的最紧迫优先事项。