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端粒酶相关基因突变携带者肺移植后生存的决定因素:一项回顾性队列研究。

Determinants of survival after lung transplantation in telomerase-related gene mutation carriers: A retrospective cohort.

机构信息

Service de Pneumologie A, Centre de référence des maladies pulmonaires rares (site constitutif), APHP, Hôpital Bichat, Paris, France.

Université de Paris and INSERM U1152, Paris, France.

出版信息

Am J Transplant. 2022 Apr;22(4):1236-1244. doi: 10.1111/ajt.16893. Epub 2021 Dec 28.

Abstract

Carriers of germline telomerase-related gene (TRG) mutations can show poor prognosis, with an increase in common hematological complications after lung transplantation (LT) for pulmonary fibrosis. The aim of this study was to describe the outcomes after LT in recipients carrying a germline TRG mutation and to identify the predictors of survival. In a multicenter cohort of LT patients, we retrospectively reviewed those carrying pathogenic TRG variations (n = 38; TERT, n = 23, TERC, n = 9, RTEL1, n = 6) between 2009 and 2018. The median age at LT was 54 years (interquartile range [IQR] 46-59); 68% were male and 71% had idiopathic pulmonary fibrosis. During the diagnosis of pulmonary fibrosis, 28 (74%) had a hematological disease, including eight with myelodysplasia. After a median follow-up of 26 months (IQR 15-46), 38 patients received LT. The overall post-LT median survival was 3.75 years (IQR 1.8-NA). The risk of death after LT was increased for patients with myelodysplasia (HR 4.1 [95% CI 1.5-11.5]) or short telomere (HR 2.2 [1.0-5.0]) before LT. After LT, all patients had anemia, 66% had thrombocytopenia, and 39% had neutropenia. Chronic lung allograft dysfunction frequency was 29% at 4 years. The present findings support the use of LT in TRG mutation carriers without myelodysplasia. Hematological evaluation should be systematically performed before LT.

摘要

携带胚系端粒酶相关基因 (TRG) 突变的患者在接受肺纤维化肺移植 (LT) 后,可能会出现预后不良,并伴有常见的血液学并发症。本研究旨在描述携带胚系 TRG 突变的 LT 受者的结局,并确定其生存率的预测因素。在一个多中心 LT 患者队列中,我们回顾性分析了 2009 年至 2018 年间携带致病性 TRG 变异的患者(n=38;TERT,n=23,TERC,n=9,RTEL1,n=6)。LT 时的中位年龄为 54 岁(四分位距 [IQR] 46-59);68%为男性,71%为特发性肺纤维化。在肺纤维化的诊断过程中,28 例(74%)患有血液系统疾病,其中 8 例患有骨髓增生异常。在中位随访 26 个月(IQR 15-46)后,38 例患者接受了 LT。LT 后总中位生存时间为 3.75 年(IQR 1.8-N/A)。LT 前患有骨髓增生异常(HR 4.1 [95%CI 1.5-11.5])或端粒较短(HR 2.2 [1.0-5.0])的患者,LT 后死亡风险增加。LT 后所有患者均出现贫血,66%出现血小板减少,39%出现中性粒细胞减少。4 年时慢性肺移植物功能障碍的发生率为 29%。目前的研究结果支持对无骨髓增生异常的 TRG 突变携带者进行 LT。LT 前应系统进行血液学评估。

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