首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Gefitinib in combination with gemcitabine and carboplatin in never smokers with non-small cell lung carcinoma: a retrospective analysis.
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Gefitinib in combination with gemcitabine and carboplatin in never smokers with non-small cell lung carcinoma: a retrospective analysis.

机译:吉非替尼联合吉西他滨和卡铂治疗非吸烟者非小细胞肺癌的回顾性分析。

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INTRODUCTION: Randomized placebo-controlled phase III trials failed to show a survival benefit with the addition of gefitinib to platinum-based combination chemotherapy as first-line therapy in unselected patients with advanced non-small cell lung cancer (NSCLC). We conducted a retrospective analysis of the outcome in never smokers with advanced NSCLC who received gemcitabine-carboplatin-gefitinib (GCI) as first-line therapy and compared these patients with a historical control group who received gemcitabine-carboplatin (GC) alone in our center. METHODS: Never-smoker patients with chemonaive stage IIIB or IV NSCLC were treated with GCI. These patients were compared with a historical control group of never smokers who had been treated with GC alone as the first-line therapy. RESULTS: A total of 80 patients were reviewed: 51 patients were treated with GCI and 29 with GC. Most patients were women, and adenocarcinoma was the most common histologic subtype. The response rate for patients in the GCI group was 62.7% (95% confidence interval [CI] = 48.08-75.87), which was higher than that of the GC group, 27.6% (95% CI = 12.73-47.24). The GCI group showed a significant improvement in progression-free survival compared with the GC group (hazard ratio of 0.19, 95% CI = 0.105-0.351, p < 0.001). The median overall survival for the patients on GCI was 20.5 months compared 14.1 months (p = 0.05) for patients on GC. CONCLUSION: The addition of gefitinib to first-line chemotherapy improved progression-free survival and overall survival when used as a first-line therapy in never smokers with advanced NSCLC in this retrospective study. A prospective randomized phase III study is needed to confirm this finding.
机译:简介:随机安慰剂对照的III期临床试验未显示出吉非替尼在铂类联合化疗中作为未选择的晚期非小细胞肺癌(NSCLC)患者的一线治疗的生存获益。我们对从未接受过吉西他滨-卡铂-吉非替尼(GCI)一线治疗的晚期NSCLC吸烟者的结局进行回顾性分析,并将这些患者与我们中心仅接受吉西他滨-卡铂(GC)的历史对照组进行了比较。方法:对不吸烟的ⅢB期或IV期NSCLC患者进行GCI治疗。将这些患者与从未接受过吸烟的历史对照组进行了比较,他们仅接受过GC作为一线治疗。结果:共检查了80例患者:51例接受GCI治疗,29例接受GC治疗。大多数患者是女性,腺癌是最常见的组织学亚型。 GCI组患者的缓解率为62.7%(95%置信区间[CI] = 48.08-75.87),高于GC组的27.6%(95%CI = 12.73-47.24)。与GC组相比,GCI组的无进展生存期有显着改善(危险比为0.19,95%CI = 0.105-0.351,p <0.001)。 GCI患者的中位总生存期为20.5个月,而GC患者为14.1个月(p = 0.05)。结论:在这项回顾性研究中,吉非替尼作为一线治疗在从未吸烟的晚期NSCLC患者中作为一线治疗时,在一线化疗中加入吉非替尼可改善无进展生存期和总生存期。需要进行前瞻性随机III期研究以证实这一发现。

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