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首页> 外文期刊>Thoracic cancer. >Tumor invasion in the central airway is a risk factor for early‐onset checkpoint inhibitor pneumonitis in patients with non‐small cell lung cancer
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Tumor invasion in the central airway is a risk factor for early‐onset checkpoint inhibitor pneumonitis in patients with non‐small cell lung cancer

机译:中央气道中的肿瘤侵袭是非小细胞肺癌患者早期起始检查点抑制剂肺炎的危险因素

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Background Anti‐programmed death‐1 (PD‐1) immunotherapy can cause immune‐related pneumonitis, also known as checkpoint inhibitor pneumonitis (CIP). CIP that develops early after the initiation of anti‐PD‐1 immunotherapy is important because it is more severe than CIP that develops later. However, only a few studies have examined the risk factors for early‐onset CIP. Previous studies have reported several risk factors for CIP, including imaging findings of airway obstruction adjacent to lung tumors. However, the utility of this factor is debatable. Therefore, we investigated potential risk factors for early‐onset CIP, including tumor invasion in the central airway (TICA), in patients with non‐small cell lung cancer (NSCLC) receiving anti‐PD‐1 therapy. Methods We retrospectively analyzed the medical records and chest computed tomography scans of patients with NSCLC treated with anti‐PD‐1 antibodies at the Kanagawa Cancer Center in Japan between 1 January 2016, and 30 June 2018. The clinical characteristics and imaging findings, including TICA, were compared between patients with and without early‐onset CIP. Results Data from 181 eligible patients (114 receiving nivolumab and 67 receiving pembrolizumab) were analyzed. Early‐onset CIP occurred in 13 of 79 patients (16.5%) with TICA and 2 of 102 patients (2.0%) without TICA. In multivariate analysis, the odds ratio of early‐onset CIP for patients with TICA was 8.2 (95% confidence interval [CI]: 1.98–34.0, P = 0.0037). Conclusions TICA was strongly associated with early‐onset CIP in patients with NSCLC. Clinicians should carefully observe patients with TICA, especially within three months of anti‐PD‐1 antibody administration because of high CIP risk. Key points Significant study findings Tumor invasion in the central airway (TICA) was a predictor of early‐onset checkpoint inhibitor pneumonitis (CIP) TICA had good interobserver variability, indicating its utility in clinical practice Patients with TICA might have a higher immune status than patients without What this study adds This is the first study focusing on risk factors for CIP limited to early‐onset CIP.
机译:背景技术抗程序死亡-1(PD-1)免疫疗法可引起免疫相关的肺炎,也称为检查点抑制剂肺炎(CIP)。抗PD-1免疫疗法开始早期发展的CIP是重要的,因为它比以后发展的CIP更严重。然而,只有少数研究检测了早盘性CIP的危险因素。以前的研究报告了CIP的几个危险因素,包括肺肿瘤附近的气道阻塞的成像结果。但是,这个因素的效用是值得简言的。因此,我们调查了早上的患者的潜在危险因素,包括中央气道(TICA)的肿瘤侵袭,接受抗PD-1治疗的非小细胞肺癌(NSCLC)。方法回顾性分析了在2016年1月1日至2018年1月1日至2018年6月30日在日本的Kanagawa癌症中心治疗NSCLC治疗NSCLC患者的病历和胸部计算断层扫描。临床特征和成像结果,包括TACA ,在患者之间进行比较和没有早发CIP的患者。结果分析了181名符合条件的患者(114种接受Nivolumab和67种接受蛋白)的数据。早盘CIP在79名患者(16.5%)中发生早上的CIP(16.5%),TICA和102名患者的2名(2.0%),没有TICA。在多变量分析中,TICA患者的早期发作CIP的差距为8.2(95%置信区间[CI]:1.98-34.0,P = 0.0037)。结论TICA与NSCLC患者的早期胶束强烈相关。临床医生应仔细观察TICA的患者,特别是由于高CIP风险,尤其在抗PD-1抗体给药的三个月内。关键点显着研究发现中央气道(TICA)的肿瘤侵袭是早发睾丸抑制剂肺炎(CIP)TICA的预测因子具有良好的Interobserver可变性,表明其在临床实践中的临床实践患者的患者可能具有比患者更高的免疫状况如果本研究添加的情况,这是第一项研究,重点关注CIP限于早盘CIP的危险因素。

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