Does combined pulmonary fibrosis and emphysema syndrome affect response to antifibrotic therapy and survival? A single-center retrospective cohort study.

Nazli Huma Teke, Meltem Agca, Ayla Turkar, Tülin Sevim, Eylem Tuncay, Sinem Gungor, Elif Yıldırım, Fatma Ozbaki, Baran Gundogus, Sibel Arınc, Huriye Berk Takır, Ipek Ozmen
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Abstract

Objective: Combined pulmonary fibrosis and emphysema (CPFE) is a clinicoradiological syndrome characterized by upper lobe emphysema and lower lobe fibrosis, most commonly associated with idiopathic pulmonary fibrosis (IPF). This study compared the clinical characteristics, functional parameters, and mortality of patients with CPFE and IPF who received antifibrotic therapy.

Methods: Between October 2015 and August 2022, patients with IPF treated with antifibrotics for at least 6 months were retrospectively evaluated and divided into two groups: CPFE (emphysema present) and IPF (emphysema absent). Demographic data, antifibrotic therapy, functional parameters before and after treatment (FEV1%, FVC%, DLco %), clinical outcomes (hospital admissions, mortality) were compared.

Results: Of the 204 patients with IPF, 90 (44%) had CPFE. CPFE patients were more often male, had greater smoking history, higher pack-years, and more lung cancer than IPF patients (p < 0.001 for all). Post-treatment FEV1% and FVC% did not significantly differ between the groups, whereas DLco% declined significantly in both (p < 0.001 and p = 0.002). DLco% decreased more in IPF than CPFE, but the difference was not statistically significant [-3 (-11-3) vs. -0.43 (-1.1-0.2), p = 0.36]. The hospital admission rates were similar. Independent risk factors for mortality included CPFE diagnosis (HR: 1.73, 95% CI: 1.06-2.83, p = 0.029), low FVC% (HR: 0.970, 95% CI: 0.96-0.98, p < 0.001), and device use (long-term oxygen therapy [LTOT]  or home non-invasive mechanical ventilation [NIMV]) (HR: 2.48, 95% CI: 1.50-4.09, p < 0.001). Mean survival was shorter in patients with emphysema than in those without emphysema (5.08 vs. 5.68 years, p = 0.08).

Conclusions: Despite a decline in DLco%, changes remained below the futility threshold. Clinical outcomes and mortality were comparable. CPFE diagnosis, low FVC%, and LTOT/NIMV use independently predicted higher mortality.

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合并肺纤维化和肺气肿综合征是否影响抗纤维化治疗的反应和生存?单中心回顾性队列研究。
目的:合并肺纤维化和肺气肿(CPFE)是一种以上肺叶肺气肿和下肺叶纤维化为特征的临床放射学综合征,最常与特发性肺纤维化(IPF)相关。本研究比较了接受抗纤维化治疗的CPFE和IPF患者的临床特征、功能参数和死亡率。方法:回顾性评估2015年10月至2022年8月期间,接受抗纤维化药物治疗至少6个月的IPF患者,并将其分为两组:CPFE(存在肺气肿)和IPF(无肺气肿)。比较人口学资料、抗纤维化治疗、治疗前后功能参数(FEV1%、FVC%、DLco %)、临床结局(住院、死亡率)。结果:在204例IPF患者中,90例(44%)发生CPFE。与IPF患者相比,CPFE患者多为男性,有更多的吸烟史,更高的包年,更多的肺癌(p < 0.001)。治疗后FEV1%和FVC%组间差异无统计学意义,DLco%组间差异有统计学意义(p < 0.001和p = 0.002)。IPF组DLco%下降幅度大于CPFE组,但差异无统计学意义[-3(-11-3)比-0.43 (-1.1-0.2),p = 0.36]。住院率相似。死亡率的独立危险因素包括CPFE诊断(HR: 1.73, 95% CI: 1.06-2.83, p = 0.029)、低FVC% (HR: 0.970, 95% CI: 0.96-0.98, p < 0.001)和设备使用(长期氧疗[LTOT]或家庭无创机械通气[NIMV]) (HR: 2.48, 95% CI: 1.50-4.09, p < 0.001)。有肺气肿患者的平均生存期短于无肺气肿患者(5.08年对5.68年,p = 0.08)。结论:尽管DLco%下降,但变化仍低于无效阈值。临床结果和死亡率具有可比性。CPFE诊断、低FVC%和LTOT/NIMV使用独立预测较高的死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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