摘要
目的:评价埃克替尼治疗晚期复发非小细胞肺癌的近期疗效及安全性。方法:回顾性分析晚期复发非小细胞肺癌患者50例资料,所有患者均口服埃克替尼125 mg,3次/d,直到病变进展或不能耐受。结果:本组50例患者均可评价疗效,客观缓解率(ORR:CR+PR)为40%,疾病控制率(DCR:CR+PR+SD)为78%。不良反应主要为皮疹和腹泻,多为Ⅰ、Ⅱ度,未见间质性肺病及血液学毒性出现。结论:埃克替尼是治疗晚期复发非小细胞肺癌NSCLC的有效药物,耐受性良好。
Objective: To evaluate the curative effect and safety of icotinib's treatment of late recurrent non-small-cell lung cancer.Methods: Retrospective analysis was conducted on 50 cases of late recurrent non-small-cell lung cancer patients. All the patients had orally taken icotinib 125 mg 3 times a day,until the disease progressed or the patients could not bear. Results: All the 50 cases were open to the evaluation of curative effect. The objective response rate( ORR: CR + PR) was 40% and the disease control rate( DCR: CR + PR+ SD) was 78%. The main adverse reactions were rash and diarrhea,mostly degree I or II. No interstitial lung disease or hematologic toxicity occurred. Conclusion: Icotinib is an effective drug for the treatment of late recurrent non-small-cell lung cancer,with an advantage of nice durability.
出处
《淮海医药》
CAS
2016年第1期34-35,42,共3页
Journal of Huaihai Medicine
关键词
癌
非小细胞肺
埃克替尼
近期疗效
安全性
Carcinoma
non-small-cell lung
Icotinib
Short-term effect
Safety