安徽医药
安徽醫藥
안휘의약
ANHUI MEDICAL AND PHARMACEUTICAL JOURNAL
2014年
11期
2174-2177
,共4页
马祥垒%史美祺%寇莹莹%汤依群
馬祥壘%史美祺%寇瑩瑩%湯依群
마상루%사미기%구형형%탕의군
肺腺癌%埃克替尼%疗效%安全性
肺腺癌%埃剋替尼%療效%安全性
폐선암%애극체니%료효%안전성
non-small cell lung adenocarcinoma%icotinib%clinical efficacy%safety
目的:观察埃克替尼用于治疗晚期肺腺癌患者的疗效及安全性,分析影响其疗效的相关因素方法回顾性分析在江苏省肿瘤医院慈善赠药点接受埃克替尼治疗90例晚期肺腺癌患者的临床资料。结果可评价疗效的90例患者中完全缓解(CR)0例,部分缓解(PR)55例(61.1%),疾病稳定(SD)28例(31.1%),疾病进展(PD)7例(7.8%),客观缓解率(ORR)为61.1%,疾病控制率(DCR)为92.2%。90例患者中位无进展生存期(PFS)为10.5(1.3~22.3)个月。已知EGFR突变阳性的40例患者中CR 0例,PR 28例(70.0%),SD 12例(30.0%)。 ORR为70.0%,DCR为100%。结论埃克替尼治疗晚期肺腺癌具有显著的疗效和良好的安全性。
目的:觀察埃剋替尼用于治療晚期肺腺癌患者的療效及安全性,分析影響其療效的相關因素方法迴顧性分析在江囌省腫瘤醫院慈善贈藥點接受埃剋替尼治療90例晚期肺腺癌患者的臨床資料。結果可評價療效的90例患者中完全緩解(CR)0例,部分緩解(PR)55例(61.1%),疾病穩定(SD)28例(31.1%),疾病進展(PD)7例(7.8%),客觀緩解率(ORR)為61.1%,疾病控製率(DCR)為92.2%。90例患者中位無進展生存期(PFS)為10.5(1.3~22.3)箇月。已知EGFR突變暘性的40例患者中CR 0例,PR 28例(70.0%),SD 12例(30.0%)。 ORR為70.0%,DCR為100%。結論埃剋替尼治療晚期肺腺癌具有顯著的療效和良好的安全性。
목적:관찰애극체니용우치료만기폐선암환자적료효급안전성,분석영향기료효적상관인소방법회고성분석재강소성종류의원자선증약점접수애극체니치료90례만기폐선암환자적림상자료。결과가평개료효적90례환자중완전완해(CR)0례,부분완해(PR)55례(61.1%),질병은정(SD)28례(31.1%),질병진전(PD)7례(7.8%),객관완해솔(ORR)위61.1%,질병공제솔(DCR)위92.2%。90례환자중위무진전생존기(PFS)위10.5(1.3~22.3)개월。이지EGFR돌변양성적40례환자중CR 0례,PR 28례(70.0%),SD 12례(30.0%)。 ORR위70.0%,DCR위100%。결론애극체니치료만기폐선암구유현저적료효화량호적안전성。
Objective To evaluate the efficacy and toxicity of icotinib,and to analyze prognostic factors influencing curative effect in patients with advanced non-small cell lung adenocarcinoma. Methods The clinical data of 90 non-small cell lung adenocarcinoma pa-tients referred to the Jiangsu Cancer Hospital were retrospectively analyzed. Results All patients were evaluable for efficacy. Among the 90 patients,there was none with complete response(CR),55 patients with partial response (PR,61. 1%),28 patients with stable disease (SD,31. 1%) and 7 patients with progression disease (PD,7. 8%). The objective response rate (ORR) was 61. 1%,and the disease control rate (DCR) was 92. 2%. The total progressive free survival was 10. 5 (1. 3~22. 3) months. Among the 40 patients with EGFR mutations,there was none with CR,28 patients with partial response ( PR,70. 0%),12 patients with stable disease ( SD, 30. 0%). The objective response rate (ORR) was 70. 0%,and the disease control rate (DCR) was 100%. Conclusions Icotinib is effective and safe in patients with advanced non-small cell lung adenocarcinoma.