Williams Kirsten M
Center for Cancer and Blood Disorders, Children's National Health System, Washington, DC; and Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Blood. 2017 Jan 26;129(4):448-455. doi: 10.1182/blood-2016-08-693507. Epub 2016 Nov 16.
In past years, a diagnosis of bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic cell transplant (HCT) conferred nearly universal mortality secondary to lack of consensus for diagnostic criteria, poorly understood disease pathogenesis, and very few studies of therapeutic or supportive care interventions. Recently, however, progress has been made in these areas: revised consensus diagnostic guidelines are now available, supportive care has improved, there is greater understanding of potential mechanisms of disease, and prospective trials are being conducted. This article describes these advances and provides suggestions to optimize therapy for patients with BOS after HCT.
在过去几年里,异基因造血细胞移植(HCT)后被诊断为闭塞性细支气管炎综合征(BOS)的患者几乎普遍死亡,原因是诊断标准缺乏共识、疾病发病机制了解不足,以及关于治疗或支持性护理干预的研究极少。然而,最近在这些领域取得了进展:现已出台修订后的共识诊断指南,支持性护理有所改善,对疾病潜在机制有了更深入的了解,并且正在进行前瞻性试验。本文描述了这些进展,并为优化HCT后BOS患者的治疗提供建议。