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Successful treatment of gefitinib-induced acute interstitial pneumonitis with high-dose corticosteroid: a case report and literature review.

机译:大剂量皮质类固醇成功治疗吉非替尼诱导的急性间质性肺炎:一例病例并文献复习。

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摘要

Cytotoxic chemotherapy offers a modest benefit for patients with advanced non-small cell lung cancer (NSCLC), with response rates of 20-35% and median survival of 10-12 months. Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs), gefitinib and erlotinib are active against lung cancer. In retrospective studies, EGFR-TKI therapy among patients harboring EGFR mutations showed response rates higher than 65% and a median survival of 20-30 months. Gefitinib is well tolerated and less toxic compared to conventional cytotoxic drugs, but gefitinib-related interstitial lung disease (ILD) has been reported as a serious adverse effect. Although the mechanism remains unknown, multivariate analysis revealed male sex, history of smoking, and the coexistence of interstitial pneumonia or pre-existence of pulmonary fibrosis and poor performance status were all significant risk factors. Here, we reported a case of gefitinib pneumonitis with severe hypoxemia and impending respiratory failure who showed poor response to intermediate dose of systemic steroids but good recovery with high-dose pulse therapy.
机译:细胞毒性化疗为晚期非小细胞肺癌(NSCLC)患者提供了适度的获益,缓解率为20-35%,中位生存期为10-12个月。表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs),吉非替尼和厄洛替尼对肺癌具有活性。在回顾性研究中,携带EGFR突变的患者中的EGFR-TKI治疗显示缓解率高于65%,中位生存期为20-30个月。与常规细胞毒性药物相比,吉非替尼具有良好的耐受性和较低的毒性,但是据报道,与吉非替尼相关的间质性肺病(ILD)具有严重的不良反应。尽管其机制仍然未知,但多因素分析显示男性,吸烟史,间质性肺炎并存或肺纤维化并存以及表现不佳均是重要的危险因素。在这里,我们报道了一例严重低氧血症和即将发生呼吸衰竭的吉非替尼肺炎,对中等剂量的全身性类固醇激素反应不良,但大剂量脉冲治疗可恢复良好。

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