尼达尼布治疗其他结缔组织疾病(CTDs)-间质性肺疾病(ILD)患者与系统性硬化症-ILD患者一样有效和安全:一项多中心回顾性研究。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-03-01 Epub Date: 2025-02-07 DOI:10.1007/s10067-025-07323-0
Salim Mısırcı, Ali Ekin, Burcu Yağız, Belkıs Nihan Coşkun, Fatma Başıbüyük, Ahmet Merih Birlik, İsmail Sarı, Aylin Dolu Karaca, Süleyman Serdar Koca, Gözde Yıldırım Çetin, Burak Okyar, Nurhan Atilla, Ediz Dalkılıç, Yavuz Pehlivan
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引用次数: 0

摘要

目的:本研究的目的是评估尼达尼布(NTD)治疗在现实世界结缔组织疾病相关间质性肺疾病(CTDs-ILD)患者中的有效性和安全性。方法:我们的多中心回顾性研究纳入了诊断为CTD-ILD的患者,这些患者在随访期间因PPF的发展而开始接受NTD治疗。对NTD治疗前、治疗开始后6、12、18个月患者的预测用力肺活量百分比(%pFVC)和预测弥散量百分比(%pDLCO)的结果进行评价。此外,将患者分为SSc-ILD和其他CTDs-ILD两组,比较NTD的疗效和安全性。结果:在所有患者(n = 66)中,与基线值相比,%pFVC和%pDLCO值在6、12和18个月后稳定下来。所有患者在NTD治疗的同时至少接受了一种免疫抑制治疗。NTD治疗后最常见的副作用是腹泻(n = 20,30.3%)。我们将患者分为SSc-ILD (n = 35)和其他ctds - ild (n = 31)两组,随访6个月、12个月和18个月时,两组间pFVC %变化(p值分别为0.498、0.595和0.376)和pDLCO %变化(p值分别为0.817、0.185和0.399)差异均无统计学意义。同样,在NTD治疗后的不良事件和安全性数据方面,两组之间无统计学差异(p < 0.05)。结论:综上所述,在SSc-ILD患者以及其他CTDs-ILD患者中,NTD联合免疫抑制治疗是有效且安全的。•这项多中心研究提供了nintedanib在结缔组织疾病-肺间质性疾病患者中使用的真实数据。•尼达尼布治疗在其他结缔组织疾病患者和系统性硬化症患者中同样有效和安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment with nintedanib is as effective and safe in patients with other connective tissue diseases (CTDs)-interstitial lung disease (ILD) as in patients with systemic sclerosis-ILD: A multicenter retrospective study.

Objective: The aim of this study is to assess the efficacy and safety of nintedanib (NTD) therapy in a real world population of patients with connective tissue diseases related interstitial lung disease (CTDs-ILD).

Methods: Our multicenter retrospective study included patients with a CTD-ILD diagnosis who started NTD treatment due to the development of PPF during follow-up. The results of the percentage predicted forced vital capacity (%pFVC) and percentage predicted diffusion capacity (%pDLCO) of patients before NTD treatment and 6, 12 and 18 months after the start of NTD treatment were evaluated. In addition, the patients were divided into two groups, SSc-ILD and other CTDs-ILD, and compared in terms of the efficacy and safety of the NTD.

Results: In all patients (n = 66), %pFVC and %pDLCO values stabilised after 6, 12 and 18 months compared to baseline values. All patients received at least one immunosuppressive therapy in combination with NTD treatment. The most common side effect after NTD treatment was diarrhoea (n = 20, 30.3%). When we divided the patients into two groups, SSc-ILD (n = 35) and other CTDs-ILDs (n = 31), no significant difference was found between the groups in the change in %pFVC (p values = 0.498, 0.595 and 0.376, respectively) and in the change in %pDLCO (p values = 0.817, 0.185 and 0.399, respectively) at 6, 12 and 18 months follow-up. Again, there was no statistically significant difference between the two groups in terms of adverse events and safety data after NTD treatment (p > 0.05).

Conclusion: In summary, the use of NTD in combination with immunosuppressive therapies was effective and safe in SSc-ILD patients as well as in other CTDs-ILD patients. Key Points • This multicenter study provides real-world data on the use of nintedanib in patients with connective tissue disease-interstitial lung disease. • Nintedanib treatment is as effective and safe in patients with other connective tissue disease as in patients with systemic sclerosis.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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