Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland.
Faculty of Medicine, University of Zurich, Zurich, Switzerland.
J Clin Apher. 2024 Jun;39(3):e22128. doi: 10.1002/jca.22128.
Due to development of chronic lung allograft dysfunction (CLAD), prognosis for patients undergoing lung transplantation (LTx) is still worse compared to other solid organ transplant recipients. Treatment options for slowing down CLAD progression are scarce with extracorporeal photopheresis (ECP) as an established rescue therapy. The aim of the study was to identify characteristics of responders and non-responders to ECP treatment, assess their survival, lung function development and by that define the subset of patients who should receive early ECP treatment.
We performed a retrospective study of all LTx patients receiving ECP treatment at the University Hospital Zurich between January 2010 and March 2020. Patients were followed-up for a maximum period of 5 years. Mortality and lung function development were assessed by CLAD stage and by CLAD subtype before initiation of ECP treatment.
Overall, 105 patients received at least one ECP following LTx. A total of 57 patients (61.3%) died within the study period with a median survival of 15 months. Mortality was 57% for patients who started ECP at CLAD1, 39% for CLAD2, 93% for CLAD3, and 90% for CLAD4 (p < 0.001). Survival and lung function development was best in young patients at early CLAD stages 1 and 2. Response to ECP treatment was worst in patients with CLAD-RAS/mixed subtype (14.3%) and patients with ECP initiation in CLAD stages 3 (7.1%) and 4 (11.1%). Survival was significantly better in a subset of patients with recurrent acute allograft dysfunction and earlier start of ECP treatment (105 vs 15 months).
In this retrospective analysis of a large group of CLAD patients treated with ECP after LTx, early initiation of ECP was associated with better long-term survival. Besides a subset of patients suffering of recurrent allograft dysfunction, especially a subset of patients defined as responders showed an improved response rate and survival, suggesting that ECP should be initiated in early CLAD stages and young patients. ECP might therefore prevent long-term disease progression even in patients with CLAD refractory to other treatment options and thus prevent or delay re-transplantation.
由于慢性肺移植物功能障碍(CLAD)的发展,肺移植(LTx)患者的预后仍然比其他实体器官移植受者差。减缓 CLAD 进展的治疗选择很少,体外光化学疗法(ECP)是一种已确立的抢救疗法。本研究的目的是确定对 ECP 治疗有反应和无反应的患者的特征,评估他们的存活率、肺功能发展,并在此基础上确定应接受早期 ECP 治疗的患者亚组。
我们对 2010 年 1 月至 2020 年 3 月在苏黎世大学医院接受 ECP 治疗的所有 LTx 患者进行了回顾性研究。患者的随访时间最长为 5 年。死亡率和肺功能发展通过 CLAD 阶段和 ECP 治疗前的 CLAD 亚型进行评估。
总体而言,105 例患者在 LTx 后至少接受了一次 ECP。在研究期间,共有 57 例(61.3%)患者死亡,中位生存期为 15 个月。CLAD1 时开始 ECP 的患者死亡率为 57%,CLAD2 时为 39%,CLAD3 时为 93%,CLAD4 时为 90%(p<0.001)。在早期 CLAD 1 期和 2 期,年轻患者的生存和肺功能发展最好。CLAD-RAS/混合亚型(14.3%)和 CLAD 3 期(7.1%)和 4 期(11.1%)开始 ECP 治疗的患者对 ECP 治疗的反应最差。在复发急性同种异体功能障碍和早期开始 ECP 治疗的患者亚组中,生存明显更好(105 个月比 15 个月)。
在对接受 LTx 后接受 ECP 治疗的大量 CLAD 患者进行的回顾性分析中,早期开始 ECP 与长期生存改善相关。除了复发性同种异体功能障碍的患者亚组外,尤其是被定义为有反应的患者亚组,反应率和生存率均有所提高,提示 ECP 应在早期 CLAD 阶段和年轻患者中开始。因此,即使对于对其他治疗选择有抵抗力的 CLAD 患者,ECP 也可能预防长期疾病进展,从而预防或延迟再次移植。