中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2013年
22期
1378-1381
,共4页
张琼%杨哲%戴洪海%王瑜%韩俊庆
張瓊%楊哲%戴洪海%王瑜%韓俊慶
장경%양철%대홍해%왕유%한준경
肺腺癌%培美曲塞%化疗%表皮生长因子受体
肺腺癌%培美麯塞%化療%錶皮生長因子受體
폐선암%배미곡새%화료%표피생장인자수체
pulmonary adenocarcinoma%pemetrexed%chemotherapy%epidermal growth factor receptor
目的:研究晚期肺腺癌EGFR突变状态对培美曲塞疗效的影响。方法:收集经病理学确诊且有可评价病灶的晚期肺腺癌患者40例,所有病例均有表皮生长因子受体(epidermal growth factor receptor,EGFR)突变状态检测结果,均采用含培美曲塞方案化疗,以总有效率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)为研究终点进行回顾性分析,比较两组间的疗效差异。结果:EGFR野生组和突变组总有效率分别为44.4%(8/18)和31.8%(7/22)(P=0.412),疾病控制率分别为88.9%(16/18)和81.8%(18/22,P=0.673)。EGFR野生组中位PFS较突变组延长(8.9 vs.5.3个月,P=0.046)。结论:晚期肺腺癌EGFR突变状态对培美曲塞的疗效有影响。
目的:研究晚期肺腺癌EGFR突變狀態對培美麯塞療效的影響。方法:收集經病理學確診且有可評價病竈的晚期肺腺癌患者40例,所有病例均有錶皮生長因子受體(epidermal growth factor receptor,EGFR)突變狀態檢測結果,均採用含培美麯塞方案化療,以總有效率(ORR)、疾病控製率(DCR)、無進展生存期(PFS)為研究終點進行迴顧性分析,比較兩組間的療效差異。結果:EGFR野生組和突變組總有效率分彆為44.4%(8/18)和31.8%(7/22)(P=0.412),疾病控製率分彆為88.9%(16/18)和81.8%(18/22,P=0.673)。EGFR野生組中位PFS較突變組延長(8.9 vs.5.3箇月,P=0.046)。結論:晚期肺腺癌EGFR突變狀態對培美麯塞的療效有影響。
목적:연구만기폐선암EGFR돌변상태대배미곡새료효적영향。방법:수집경병이학학진차유가평개병조적만기폐선암환자40례,소유병례균유표피생장인자수체(epidermal growth factor receptor,EGFR)돌변상태검측결과,균채용함배미곡새방안화료,이총유효솔(ORR)、질병공제솔(DCR)、무진전생존기(PFS)위연구종점진행회고성분석,비교량조간적료효차이。결과:EGFR야생조화돌변조총유효솔분별위44.4%(8/18)화31.8%(7/22)(P=0.412),질병공제솔분별위88.9%(16/18)화81.8%(18/22,P=0.673)。EGFR야생조중위PFS교돌변조연장(8.9 vs.5.3개월,P=0.046)。결론:만기폐선암EGFR돌변상태대배미곡새적료효유영향。
Objective:To assess the role of EGFR mutations on pemetrexed response in patients with advanced lung adenocarcino-ma. Method: Forty pulmonary adenocarcinoma patients with evaluable lesions were retrospectively screened .They had been treated with pemetrexed-included chemotherapy and had EGFR gene test results. The evaluation endpoints were overall response rate,disease control rate and progression free survival. Result:No significant statistical difference was seen in overall response rate(ORR) (44.4%VS 31.8%, respectively) and disease control rate(DCR) (88.9%VS 81.8%, respectively ) between EGFR wild group and EGFR muta-tion group, but patients in EGFR wild group had longer progression free survival(PFS) ( 8.9 months VS 5.3 months;P=0.046). Conclu-sion:EGFR mutation status can influence the efficacy of pemetrexed.