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机构地区:[1]皖南医学院第一附属医院,安徽芜湖241000
出 处:《肿瘤学杂志》2016年第3期176-179,共4页Journal of Chinese Oncology
摘 要:[目的]探讨盐酸埃克替尼治疗晚期非小细胞肺癌(NSCLC)的临床疗效及不良反应。[方法 ]回顾性分析45例经病理学确诊的晚期NSCLC患者临床资料及埃克替尼治疗的临床疗效和不良反应。所有患者均口服盐酸埃克替尼片,125mg/次,3次/d,直至病情进展或出现不能耐受的不良反应。[结果]45例患者治疗1个周期后,完全缓解(CR)0例,部分缓解(PR)20例(44.4%),疾病稳定(SD)15例(33.3%),疾病进展(PD)10例(22.2%),客观有效率(ORR)为44.4%(20/45),疾病控制率(DCR)为77.8%(35/45),中位无进展生存期(m PFS)为6.3个月(95%CI:3.6~9.0),中位总生存期(m OS)为15.2个月(95%CI:11.3~19.0)。治疗相关不良反应主要为皮疹4例(8.9%),腹泻及胃部不适2例(4.4%),肝功能损害2例(4.4%)。盐酸埃克替尼治疗的疗效与吸烟史有关(P〈0.05)。[结论]盐酸埃克替尼治疗晚期NSCLC疗效肯定,具有毒性低、安全性高、耐受性好的特点,作为新的表皮生长因子受体—酪氨酸激酶抑制剂,为晚期NSCLC患者的治疗提供了新选择。[Purpose] To investigate the efficacy and toxicities of icotinib hydrochloride in the treatment of patients with advanced non-small cell lung cancer(NSCLC). [Methods] The clinical data,efficacy and toxicities of icotinib hydrochloride in the treatment of 45 cases with advanced NSCl C were analyzed retrospectively.Patients were treated with icotinib hydrochloride(125mg,3times a day) untill disease progression or intolerance with toxicities. [Results] After one period of treatment,zero cases showed compelet response(CR);20 cases(44.4%)showed partial response(PR);15 cases(33.3%) achieved stable disease(SD);and 10 cases(22.2%)had progressive disease(PD).The objective response rate(ORR) was 44.4%(20/45),and disease control rate(DCR) was77.8%(35/45).The media progression free survival(m PFS) was 6.3 months,and the media overall survival(m OS) was 15.2 months. The major toxicities were skin rash(4 cases,8.9%),diarrhea and stomach upset(2 cases,4.4%).Two patients had liver damage(4.4%).The efficacy of icotinib hydrochloride was associated with the smoking history(P0.05).[Conclusion] Icotinib hydrochioride is effective in the treatment for advanced NSCLC,with low toxicity,good safety and tolerability.As a new epidermal growth Factor receptor-tyrosine kinase inhibitor(EGFR-TKI),it provides a new choice for patients with advanced NSCLC.
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