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首页> 外文期刊>Seminars in Hematology >Late pulmonary complications after allogeneic hematopoietic stem cell transplantation: Diagnosis, monitoring, prevention, and treatment
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Late pulmonary complications after allogeneic hematopoietic stem cell transplantation: Diagnosis, monitoring, prevention, and treatment

机译:异基因造血干细胞移植后的晚期肺部并发症:诊断,监测,预防和治疗

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Bronchiolitis obliterans syndrome (BOS) is a life-threatening complication that occurs among recipients of allogeneic lung and hematopoietic stem cell transplantation (allo-HSCT). BOS usually occurs within the first 2 years but may develop as late as 5 years after allo-HSCT. Recent prevalence estimates suggest that BOS is likely underdiagnosed in the clinical setting and that 14% of all long-term survivors with chronic graft-versus-host disease (GVHD) may develop BOS. It is difficult to diagnose and once respiratory symptoms appear, most allo-HSCT recipients show severe airflow obstruction. This may be due, at least in part, to the low sensitivity of standard spirometry in detecting small airways obstruction and lack of formal recommendations for screening for this complication. The prognosis of BOS is poor with reported 5-year survival of about 15%. A key obstacle in advancing clinical research in BOS is the lack of diagnostic and therapeutic response standards, making interpretation of survival and treatment results between studies difficult. This situation has significantly improved due to the introduction of the National Institutes of Health (NIH) criteria, which provide investigators with common definitions for studying BOS and for assessing the effects of therapeutic interventions. Future advances in the therapy of BOS may need to include development of better early intervention strategies based on identification of reliable early biological markers of the disease. It would be also important to improve understanding of the biological heterogeneity of this devastating complication after allo-HSCT.
机译:闭塞性细支气管炎综合征(BOS)是一种威胁生命的并发症,发生于同种异体肺和造血干细胞移植(allo-HSCT)的接受者之间。 BOS通常在头2年内发生,但可能会在all-HSCT之后发展到5年。最近的患病率估计表明,在临床情况下BOS可能未得到充分诊断,所有患有慢性移植物抗宿主病(GVHD)的长期幸存者中有14%可能会形成BOS。这很难诊断,一旦出现呼吸道症状,大多数异体-HSCT受体就会出现严重的气流阻塞。这可能至少部分是由于标准肺活量测定法在检测小气道阻塞中的敏感性低以及缺乏针对这种并发症进行筛查的正式建议。 BOS的预后较差,据报道其5年生存率约为15%。推进BOS临床研究的主要障碍是缺乏诊断和治疗反应标准,这使得研究之间难以解释生存和治疗结果。由于引入了美国国立卫生研究院(NIH)标准,这种情况已大大改善,该标准为研究人员提供了研究BOS和评估治疗干预效果的通用定义。 BOS治疗的未来进展可能需要包括基于对疾病可靠的早期生物学标记物的鉴定,开发更好的早期干预策略。在异基因造血干细胞移植后,进一步了解这种破坏性并发症的生物学异质性也很重要。

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