首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Phase II trial of gefitinib alone without radiation therapy for Japanese patients with brain metastases from EGFR-mutant lung adenocarcinoma
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Phase II trial of gefitinib alone without radiation therapy for Japanese patients with brain metastases from EGFR-mutant lung adenocarcinoma

机译:单用吉非替尼不进行放射治疗的II期临床试验用于日本患有EGFR突变型肺腺癌的脑转移患者

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Background: Brain metastases (BM) are a common in patients with lung cancer. Although whole-brain radiation therapy (WBRT) is the standard therapy, it may have a risk of decline in cognitive function of patients. In this study, we evaluated the efficacy of gefitinib alone without radiation therapy for the treatment of patients with BM from lung adenocarcinoma. Materials and methods: Eligible patients had BM from lung adenocarcinoma with epidermal growth factor receptor (EGFR) mutations. Gefitinib was given at 250. mg orally once a day until tumor progression or unacceptable toxicity. Results: Forty-one patients were enrolled. The response rate was 87.8%. No patient experienced grade ≥4 toxicity. The median progression-free survival time was 14.5 months (95% CI, 10.2-18.3 months), and the median overall survival time was 21.9 months (95% CI, 18.5-30.3 months). In compared with L858R, exon 19 deletion was associated with better outcome of patients after treatment with gefitinib in both progression-free (p= 0.003) and overall survival (p= 0.025). Conclusion: Favorable response of BM to gefitinib even without irradiation was demonstrated. Exon 19 deletion was both a predictive and prognostic marker of patients with BM treated by gefitinib.
机译:背景:脑转移瘤(BM)在肺癌患者中很常见。尽管全脑放射疗法(WBRT)是标准疗法,但可能存在患者认知功能下降的风险。在这项研究中,我们评估了未经放射治疗的吉非替尼单独治疗肺腺癌BM的疗效。材料和方法:符合条件的患者患有肺腺癌,其表皮生长因子受体(EGFR)突变。吉非替尼每天口服一次250. mg,直至肿瘤进展或出现不可接受的毒性。结果:招募了41例患者。回应率为87.8%。没有患者经历≥4级毒性。中位无进展生存时间为14.5个月(95%CI,10.2-18.3个月),中位总生存时间为21.9个月(95%CI,18.5-30.3个月)。与L858R相比,吉非替尼治疗后在无进展(p = 0.003)和总生存(p = 0.025)方面,外显子19缺失与患者更好的预后相关。结论:即使没有照射,BM对吉非替尼的反应良好。外显子19缺失是吉非替尼治疗的BM患者的预测和预后标志物。

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