Division of Pediatric Hematology/Oncology, Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
Clin Transplant. 2011 Mar-Apr;25(2):E168-76. doi: 10.1111/j.1399-0012.2010.01357.x. Epub 2010 Nov 16.
Late onset non-infectious pulmonary complications (LONIPCs) are major causes of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). We evaluated the incidence and the outcomes of LONIPCs in children who underwent allo-HSCT.
Data for 143 children who underwent allo-HSCT at Asan Medical Center between April 2002 and April 2009 were reviewed, and the 127 who survived more than three months were enrolled.
Eleven (8.7%) developed LONIPCs at a median eight months (range 3-14 months) after allo-HSCT, presenting with cough and dyspnea. Six had bronchiolitis obliterans and five had idiopathic pneumonia syndrome. FVC declined more significantly in LONIPC than in non-LONIPC patients three months after HSCT. A significant risk factor for the development of LONIPCs was chronic graft-versus-host disease (GVHD) (p = 0.002). At a median follow-up of 36 months, the three-yr overall survival rate in LONIPC patients was significantly lower than that of non-LONIPC patients (37.4% vs. 72.7%, p = 0.02). The major cause of death was respiratory failure.
Along with chronic GVHD, deterioration of pulmonary function at three months after HSCT may help in the early identification of patients at risk of subsequent LONIPCs. Considering the poor prognosis of LONIPC, strategies should be aimed at their prevention.
异基因造血干细胞移植(allo-HSCT)后,迟发性非感染性肺部并发症(LONIPCs)是发病率和死亡率的主要原因。我们评估了接受 allo-HSCT 的儿童 LONIPCs 的发生率和结局。
回顾了 2002 年 4 月至 2009 年 4 月在 Asan 医疗中心接受 allo-HSCT 的 143 例儿童的数据,纳入了 127 例存活时间超过 3 个月的患者。
11 例(8.7%)在 allo-HSCT 后中位 8 个月(3-14 个月)出现 LONIPCs,表现为咳嗽和呼吸困难。6 例为闭塞性细支气管炎,5 例为特发性肺炎综合征。HSCT 后 3 个月,LONIPC 患者的 FVC 下降更为明显。慢性移植物抗宿主病(GVHD)是 LONIPC 发生的显著危险因素(p=0.002)。中位随访 36 个月后,LONIPC 患者的 3 年总生存率明显低于非 LONIPC 患者(37.4%vs.72.7%,p=0.02)。死亡的主要原因是呼吸衰竭。
除慢性 GVHD 外,HSCT 后 3 个月肺功能恶化可能有助于早期识别有发生后续 LONIPC 风险的患者。鉴于 LONIPC 的预后较差,应采取策略预防其发生。