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Outcome and treatment of late-onset noninfectious pulmonary complications after allogeneic haematopoietic SCT.

机译:异基因造血SCT后迟发性非感染性肺并发症的结果和治疗。

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Late-onset noninfectious pulmonary complications (LONIPCs) are life threatening for allogeneic hematopoietic SCT (allo-HSCT) recipients. However, the impact of LONIPCs on survival has not been properly evaluated and little is known about treatment efficacy. We retrospectively investigated 290 allo-HSCT recipients in our institute and reviewed the clinical aspects of 44 patients who had been diagnosed with LONIPCs. LONIPCs were significantly associated with higher rates of chronic GVHD (P<0001) and nonrelapse mortality (P=0.013), and lower rates of relapse (P=0.009). As a result of these effects, OS was significantly worse in those with LONIPCs (P=0.003). This result differs from a previous report. We then assessed short-term treatment response and final outcome. These results were defined by radiological findings, subjective symptoms, oxygen requirement and survival. Use of inhaled and systemic steroids did not affect either short-term response or final outcomes. However, administration of systemic corticosteroids earlier than at 21 days (median interval of time from onset of symptoms to systemic corticosteroids administration) was associated with a better outcome (P=0.054 for short-term response, and 0.016 for final outcome). Our study indicates that LONIPCs reduce OS, and early intervention with systemic corticosteroids may be effective.
机译:迟发性非感染性肺部并发症(LONIPC)对异基因造血SCT(allo-HSCT)受体的生命造成威胁。但是,尚未正确评估LONIPC对生存的影响,对治疗功效知之甚少。我们回顾性研究了该研究所的290名allo-HSCT接受者,并回顾了诊断为LONIPC的44例患者的临床情况。 LONIPC与慢性GVHD发生率较高(P <0001)和非复发死亡率(P = 0.013)和较低的复发率(P = 0.009)显着相关。这些影响的结果是,在患有LONIPC的患者中OS显着恶化(P = 0.003)。此结果与以前的报告不同。然后,我们评估了短期治疗反应和最终结果。这些结果由放射学结果,主观症状,需氧量和生存期定义。吸入和全身性类固醇的使用不会影响短期反应或最终结局。但是,在21天(从症状发作到全身应用皮质类固醇激素的中位时间间隔)之前,较早施用全身性皮质类固醇与较好的预后相关(短期反应为P = 0.054,最终结果为0.016)。我们的研究表明,LONIPC可降低OS,并且早期用全身性皮质类固醇干预可能是有效的。

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