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埃克替尼治疗30例晚期非小细胞肺癌的近期疗效及安全性分析 被引量:7

The clinical efficacy and tolerability of Icotinib in 30 advanced NSCLC patients
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摘要 目的:探讨埃克替尼治疗30例NSCLC患者的近期疗效及安全性。方法:对30例患者进行随访,治疗方法为每次125mg,每日3次,口服埃克替尼药物,收集用药后2个月及4个月疗效评价及不良反应。结果:2个月疗效评价PR17例,SD7例,PD6例,客观有效率56.7%,疾病控制率80%;4个月PR15例,SD5例,PD11例,客观有效率51.7%,疾病控制率68.9%;不良反应主要是皮疹及腹泻,仅皮疹有3例Ⅲ~Ⅳ度。结论:埃克替尼治疗晚期NSCLC具有较好的近期疗效及安全性。 Objective: Evaluate the clinical efficacy and tolerability of Icotinib in thirty advanced NSCLC patients.Methods: Thirty NSCLC patients were treated with Icotinib 125mg three times a day until disease progression or unacceptable toxicity.Results: By two months,the objective response rate(ORR)was 56.7% and disease control rate(DCR)was 80%,including partial response(PR) of 17 cases,stable disease(SD) of 7 cases and progressive disease(PD) of 6 cases.By four months,the ORR was 51.7% and DCR was 68.9%,including PR of 15 cases,SD of 5 cases and PD of 11 cases.Adverse reaction is mainly rash and diarrhea.Conclusion: Icotinib have better curative effect and insignificant adverse reaction in the treatment of NSCLC.
出处 《药品评价》 CAS 2012年第30期24-27,共4页 Drug Evaluation
关键词 非小细胞肺癌 靶向治疗 EGFRTKI 埃克替尼 近期疗效 不良反应 NSCLC Targeted therapy EGFR-TKI Icotinib Short-term effect Adverse reaction
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