Glasgow prognostic score and body mass index predict short-term discontinuation of the antifibrotic agents pirfenidone and nintedanib

IF 2.4 Q2 RESPIRATORY SYSTEM Respiratory investigation Pub Date : 2024-03-08 DOI:10.1016/j.resinv.2024.02.012
Kazutaka Takehara , Yasuhiko Koga , Yoshimasa Hachisu , Mitsuyoshi Utsugi , Yuri Sawada , Yasuyuki Saito , Seishi Yoshimi , Masakiyo Yatomi , Hiroaki Tsurumaki , Yuki Shin , Ikuo Wakamatsu , Norimitsu Kasahara , Koichi Yamaguchi , Kazue Umetsu , Shunichi Kouno , Junichi Nakagawa , Noriaki Sunaga , Toshitaka Maeno , Takeshi Hisada
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Abstract

Background

The antifibrotic agents pirfenidone and nintedanib have been shown to be effective in patients with idiopathic pulmonary fibrosis (IPF). However, discontinuation of antifibrotic drugs is a major clinical concern because of the lack of alternative treatment options. Therefore, we identified factors that may be useful for predicting the termination of antifibrotic agents.

Methods

We retrospectively recruited 280 IPF patients treated with antifibrotic drugs between 2009 and 2018 from seven regional core hospitals in Gunma prefecture, Japan. Results: At four months, the short-term discontinuation group exhibited a significantly worse prognosis in the pirfenidone group and a poorer prognosis in the nintedanib group compared to that in the continuation group. The discontinuation group of pirfenidone at 4 months exhibited lower albumin and higher C-reactive protein (CRP) levels in the sera compared to the group that continued treatment for more than 4 months. In multivariate analysis, the Glasgow prognostic score (GPS), well known as a predictor of cancer prognosis, which comprises serum CRP and albumin levels, predicted early discontinuation and prognosis in the pirfenidone group, whereas the body mass index (BMI) predicted early discontinuation of nintedanib. A high GPS, with both albumin <3.5 g/dL and CRP >1.0 mg/dL, was associated with a poorer prognosis in the pirfenidone group.

Conclusion

GPS and BMI were significant factors for short-term pirfenidone and nintedanib discontinuation, respectively. Initial evaluation of GPS and BMI prior to antifibrotic therapy may contribute to less interrupted IPF management, thus leading to better prognostic outcomes in patients with IPF.

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格拉斯哥预后评分和体重指数可预测抗纤维化药物吡非尼酮和宁替尼的短期停药情况
背景抗纤维化药物吡非尼酮(pirfenidone)和宁替达尼(nintedanib)已被证明对特发性肺纤维化(IPF)患者有效。然而,由于缺乏替代治疗方案,停用抗纤维化药物是临床关注的一个主要问题。因此,我们确定了可能有助于预测抗纤维化药物停药的因素。方法我们回顾性招募了 2009 年至 2018 年期间在日本群马县 7 家地区核心医院接受抗纤维化药物治疗的 280 名 IPF 患者。结果与继续用药组相比,短期停药组在4个月后的预后明显差于吡非尼酮组,而宁替尼组的预后较差。与继续治疗超过4个月的组别相比,停药4个月的吡非尼酮组血清中白蛋白水平较低,C反应蛋白(CRP)水平较高。在多变量分析中,由血清 CRP 和白蛋白水平组成的格拉斯哥预后评分(GPS)是众所周知的癌症预后预测指标,它预测了吡非尼酮组的早期停药和预后,而体重指数(BMI)则预测了宁替尼组的早期停药。结论GPS和BMI分别是导致吡非尼酮和宁替尼短期停药的重要因素。在抗纤维化治疗前对 GPS 和 BMI 进行初步评估可能有助于减少 IPF 管理的中断,从而改善 IPF 患者的预后。
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来源期刊
Respiratory investigation
Respiratory investigation RESPIRATORY SYSTEM-
CiteScore
4.90
自引率
6.50%
发文量
114
审稿时长
64 days
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