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首页> 外文期刊>Journal of Clinical Oncology >Prospective study of gefitinib in epidermal growth factor receptor fluorescence in situ hybridization-positive/phospho-Akt-positive or never smoker patients with advanced non-small-cell lung cancer: the ONCOBELL trial.
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Prospective study of gefitinib in epidermal growth factor receptor fluorescence in situ hybridization-positive/phospho-Akt-positive or never smoker patients with advanced non-small-cell lung cancer: the ONCOBELL trial.

机译:吉非替尼在表皮生长因子受体荧光原位杂交阳性/磷酸化Akt阳性或从不吸烟的晚期非小细胞肺癌患者中的前瞻性研究:ONCOBELL试验。

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PURPOSE: In non-small-cell lung cancer (NSCLC), clinical and biologic predictors for epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor sensitivity have been identified in retrospective studies, and there is urgent need to validate these results in prospective trials. The ONCOBELL trial is a prospective phase II study evaluating gefitinib sensitivity in NSCLC patients who never smoked or have increased EGFR gene copy number or activation of the antiapoptotic protein Akt. PATIENTS AND METHODS: EGFR gene copy number was evaluated using fluorescence in situ hybridization (FISH), and presence of phospho-Akt was evaluated using immunohistochemistry. Additional tests included immunohistochemistry analysis of EGFR, FISH analysis of HER2, and mutation analysis of EGFR, HER2, and K-ras. RESULTS: From November 2004 to February 2006, 183 patients were screened, and 42 patients were enrolled onto the trial. We observed one complete and 19 partial responses, for an overall response rate (RR) of 47.6%(95% CI, 32.5% to 62.7%). Median duration of response was 6.1 months, median time to progression (TTP) was 6.4 months, 1-year survival rate was 64.3%, and median survival time was not reached. EGFR FISH-positive patients, compared with negative patients, had higher RR (68.0% v 9.1%, respectively; P < .001), longer TTP (7.6 v 2.7 months, respectively; P = .02), and a trend for longer survival (median survival not reached v 7.4 months, respectively; P = .3). Therapy was well tolerated, and there were no drug-related deaths. Median follow-up time was too short for significance tests of differences in survival outcomes. CONCLUSION: Gefitinib is active and well tolerated in patients with trial characteristics, and EGFR FISH analysis is an accurate predictor for such therapy.
机译:目的:在非小细胞肺癌(NSCLC)中,在回顾性研究中已经确定了表皮生长因子受体(EGFR)酪氨酸激酶抑制剂敏感性的临床和生物学预测指标,迫切需要在前瞻性试验中验证这些结果。 ONCOBELL试验是一项前瞻性II期研究,评估了从未吸烟或EGFR基因拷贝数增加或抗凋亡蛋白Akt活化的NSCLC患者中的吉非替尼敏感性。病人和方法:使用荧光原位杂交(FISH)评估EGFR基因拷贝数,并使用免疫组织化学评估磷酸化Akt的存在。其他测试包括EGFR的免疫组织化学分析,HER2的FISH分析以及EGFR,HER2和K-ras的突变分析。结果:从2004年11月到2006年2月,筛查了183例患者,其中42例患者入选了该试验。我们观察到一个完整的反应和19个部分反应,总反应率(RR)为47.6%(95%CI,32.5%至62.7%)。中位缓解时间为6.1个月,中位进展时间(TTP)为6.4个月,一年生存率为64.3%,未达到中位生存时间。与阴性患者相比,EGFR FISH阳性患者的RR较高(分别为68.0%v 9.1%; P <.001),TTP较长(分别为7.6 v 2.7个月; P = .02),并且趋势更长生存率(中位生存率分别未达到7.4个月; P = 0.3)。治疗耐受性良好,没有与药物有关的死亡。对于生存结局差异的显着性检验,中位随访时间太短。结论:吉非替尼在具有试验特征的患者中活跃且耐受性良好,EGFR FISH分析是此类疗法的准确预测指标。

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