風濕

結締組織病相關間質性肺病患者發生肺癌的危險因素是肺氣腫及未用免疫抑製劑

作者:Satoshi W, et al 翻譯:北醫三院魏慧(weihui2012@bjmu.edu.cn) 來源:中國風濕病公眾論壇 日期:2018-06-07
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         結締組織病相關間質性肺病患者發生肺癌的危險因素是肺氣腫及未用免疫抑製劑

關鍵字:  間質性肺病 

        摘要:背景:肺癌(LC)對特發性肺纖維化患者的生存有不利影響。然而,對於肺癌在結締組織病相關的間質性肺病(CTD-ILD)患者中的情況目前知之甚少。本研究的目的在於評估CTD-ILD患者中肺癌的患病率和危險因素,以及CTD-ILD患者的臨床特點和生存率。方法:我們對2003年至2016年的CTD-ILD患者進行了單中心回顧性研究。經病理判定患者是否罹患肺癌。觀察肺癌的患病率、危險因素、臨床特點以及對CTD-ILD患者預後的影響。結果:266例CTD-ILD患者中,24例(9.0%)有肺癌。高齡、男性、吸煙、類風濕關節炎病史、普通型間質性肺炎、肺氣腫、肺一氧化碳彌散功能(DLco)低於預測值、未接受免疫抑製治療,都是CTD-ILD患者肺癌的易患因素。多因素分析表明,肺氣腫[比值比(OR值)為8.473%;95%置信區間(CI),2.241-32.033]和不使用免疫抑製療法(OR,8.111;95%CI,2.457-26.775)是肺癌的獨立危險因素。有肺癌的CTD-ILD患者的生存率顯著低於無肺癌的患者(10年生存率:28.5% vs. 81.8%,P<0.001)。結論:CTD-ILD患者肺癌的發生與肺氣腫及不使用免疫抑製治療有關,肺癌增加了CTD-ILD患者的死亡率。

        附原文:Backgrounds: Lung cancer (LC) adversely impacts survival in patients with idiopathic pulmonary fibrosis. However, little is knownabout LC in patients with connective tissue disease-associated interstitial lung disease (CTD-ILD). The aim of this study was to evaluate the prevalence of and risk factors for LC in CTD-ILD, and the clinical characteristics and survival of CTD-ILD patients with LC.Methods: We conducted a single-center, retrospective review of patients with CTD-ILD from 2003 to 2016. Patients with pathologically diagnosed LC were identified. The prevalence, risk factors, and clinical features of LC and the impact of LC on CTD-ILD patients outcomes were observed.Results: Of 266 patients with CTD-ILD, 24 (9.0%) had LC. CTD-ILD with LC was more likely in patients who were older, male, and smokers; had rheumatoid arthritis, a usual interstitial pneumonia pattern, emphysema on chest computed tomography scan, and lower diffusing capacity of the lung carbon monoxide (DLco)% predicted; and were not receiving immunosuppressive therapy. Multivariate analysis indicated that the presence of emphysema [odds ratio (OR), 8.473%; 95% confidence interval (CI), 2.241-32.033] and nonuse of immunosuppressive therapy (OR, 8.111; 95% CI, 2.457-26.775) were independent risk factors for LC. CTD-ILD patients with LC had significantly worse survival than patients without LC (10-year survival rate: 28.5% vs. 81.8%, P<0.001).Conclusions: LC is associated with the presence of emphysema and nonuse of immunosuppressive therapy, and contributes to increased mortality in patients with CTD-ILD.

        引自:Satoshi W, Keigo S, Yoko W, et al. Lung cancer in connective tissue disease-associated interstitial lung disease: clinical features and impact on outcomes. Journal of Thoracic Disease, 2018, 10(2): 799-807. DOI: 10.21037/jtd.2017.12.134.

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