Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Cancer Sci. 2011 May;102(5):1032-7. doi: 10.1111/j.1349-7006.2011.01887.x. Epub 2011 Feb 28.
The efficacy of gefitinib for patients with non-adenocarcinoma non-small-cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutations is unclear, because only a small percentage of patients enrolled in the clinical trials to evaluate the efficacy of gefitinib for tumors harboring EGFR mutation were non-adenocarcinoma NSCLC. A pooled analysis was conducted to clarify the efficacy of gefitinib for non-adenocarcinoma NSCLC patients harboring EGFR mutations. A systematic search of the PUBMED databases was conducted to identify all clinical reports that contained advanced non-adenocarcinoma NSCLC patients harboring EGFR mutations and treated with gefitinib. The selected patients were advanced non-adenocarcinoma NSCLC patients harboring EGFR mutations who were treated with gefitinib and described in reports containing the data of the histology, status of EGFR mutations and response to gefitinib. This study selected 33 patients from 15 reports. Twenty-seven and three of the 33 patients were squamous cell carcinoma and adenosquamous cell carcinoma, respectively. One patient each had large-cell carcinoma, pleomorphic carcinoma and spindle cell carcinoma. Twenty-one patients (64%) had sensitive EGFR mutations. The response rate (RR), disease control rate (DCR) and median progression-free survival (mPFS) was 27%, 67-70% and 3.0 months, respectively. These factors were statistically significantly inferior in the non-adenocarcinoma NSCLC patients harboring EGFR mutations to adenocarcinoma patients harboring EGFR mutations selected from the same published reports (RR: 27%vs 66%, P = 0.000028; DCR: 67-70%vs 92-93%, P = 0.000014; mPFS: 3.0 vs 9.4 months, P = 0.0001, respectively). Gefitinib is less effective in non-adenocarcinoma NSCLC harboring EGFR mutations than adenocarcinoma harboring EGFR mutations.
吉非替尼治疗携表皮生长因子受体(EGFR)突变的非腺癌非小细胞肺癌(NSCLC)患者的疗效尚不清楚,因为评估吉非替尼治疗携 EGFR 突变肿瘤疗效的临床试验中只有一小部分入组患者为非腺癌 NSCLC。本研究通过汇总分析明确了携 EGFR 突变的非腺癌 NSCLC 患者应用吉非替尼的疗效。通过对 PUBMED 数据库进行系统检索,确定了所有包含 EGFR 突变的晚期非腺癌 NSCLC 患者接受吉非替尼治疗的临床报告。本研究选择了组织学、EGFR 突变状态和吉非替尼治疗反应数据均有详细报告的晚期非腺癌 NSCLC 患者,这些患者均接受了吉非替尼治疗。本研究共从 15 项研究中选择了 33 例患者,其中 33 例患者中 27 例为鳞状细胞癌,3 例为腺鳞癌,1 例为大细胞癌、多形性癌和梭形细胞癌。21 例(64%)患者存在敏感 EGFR 突变。客观缓解率(RR)、疾病控制率(DCR)和中位无进展生存期(mPFS)分别为 27%、67-70%和 3.0 个月。与从同一批发表报告中选择的 EGFR 突变腺癌患者相比,这些因素在携 EGFR 突变的非腺癌 NSCLC 患者中明显更差(RR:27%vs66%,P =0.000028;DCR:67-70%vs92-93%,P =0.000014;mPFS:3.0 vs9.4 个月,P =0.0001)。与 EGFR 突变腺癌患者相比,携 EGFR 突变的非腺癌 NSCLC 患者应用吉非替尼的疗效更差。