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首页> 外文期刊>Clinical lung cancer >Gefitinib as first-line treatment in elderly epidermal growth factor receptor-mutated patients with advanced lung adenocarcinoma: results of a Nagano Lung Cancer Research Group study.
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Gefitinib as first-line treatment in elderly epidermal growth factor receptor-mutated patients with advanced lung adenocarcinoma: results of a Nagano Lung Cancer Research Group study.

机译:吉非替尼作为老年表皮生长因子受体突变的晚期肺腺癌患者的一线治疗:长野县肺癌研究小组的一项研究结果。

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Efficacy of first-line gefitinib for elderly epidermal growth factor receptor mutated patients with lung adenocarcinoma is uncertain. This study was aimed to investigate efficacy of gefitinib for such population. The primary endpoint was response rate (RR) and at least 12 cases were needed. Overall RR was 59% (95% confidence interval, 33%-81%) and first-line gefitinib was effective for elderly patients. INTRODUCTION: Feasibility of gefitinib therapy in elderly patients with non-small-cell lung cancer is uncertain. This phase II study aimed to investigate the efficacy and usefulness of gefitinib therapy as a first-line treatment for elderly patients who have advanced lung adenocarcinoma with epidermal growth factor receptor (EGFR) mutations. PATIENTS AND METHODS: We enrolled chemotherapy-naive advanced lung adenocarcinoma patients aged 75 years or older. Patients were administered gefitinib (250 mg) once daily until progression or unacceptable toxicity. The primary endpoint was response rate (RR), and secondary endpoints were disease control rate (DCR; defined as complete response [CR] plus partial response [PR] plus stable disease [SD]), progression-free survival (PFS), overall survival (OS), and toxicity profile. RESULTS: Between April 2008 and November 2009, 17 lung adenocarcinoma patients were enrolled. Overall RR was 59% (95% confidence interval [CI]: 33% to 81%), with 2 patients achieving CR and 8 PR. SD was noted in 5 patients, and DCR was 88% (95% CI: 62% to 98%). Median PFS was 12.9 months (95% CI: 2.2 to 23.6 months), and median OS had not yet been reached. Major grade 3 toxicities were skin rash (12%) and increased levels of aspartate aminotransferase or alanine aminotransferase (18%). CONCLUSION: First-line treatment with gefitinib was effective and well-tolerated in elderly patients with EGFR mutations.
机译:一线吉非替尼对老年表皮生长因子受体突变的肺腺癌患者的疗效尚不确定。这项研究旨在调查吉非替尼对这类人群的疗效。主要终点是缓解率(RR),至少需要12例。总体RR为59%(95%置信区间,33%-81%),一线吉非替尼对老年患者有效。简介:吉非替尼治疗老年非小细胞肺癌患者的可行性尚不确定。这项II期研究旨在研究吉非替尼疗法作为具有表皮生长因子受体(EGFR)突变的晚期肺腺癌的老年患者的一线治疗的疗效和实用性。患者和方法:我们招募了年龄在75岁或以上的单纯化疗的晚期肺腺癌患者。每天给患者服用吉非替尼(250 mg)一次,直至进展或出现不可接受的毒性。主要终点为缓解率(RR),次要终点为疾病控制率(DCR;定义为完全缓解[CR]加上部分缓解[PR]加上稳定疾病[SD]),无进展生存期(PFS),总体存活率(OS)和毒性。结果:2008年4月至2009年11月,共有17例肺腺癌患者入组。总体RR为59%(95%置信区间[CI]:33%至81%),其中2例患者获得CR,8例PR。 5名患者出现SD,DCR为88%(95%CI:62%至98%)。 PFS中位数为12.9个月(95%CI:2.2至23.6个月),而OS尚未达到中位数。 3级主要毒性为皮疹(12%)和天冬氨酸转氨酶或丙氨酸转氨酶水平升高(18%)。结论:吉非替尼一线治疗对EGFR突变的老年患者有效且耐受性良好。

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