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作 者:武要洪[1] 孙传政[1] 李晓江[1] 邓莅霏[2] 李科[1] 费继敏[1] 王虎[1]
机构地区:[1]云南省肿瘤医院,云南昆明650118 [2]江西省肿瘤医院头颈科,江西南昌330029
出 处:《现代肿瘤医学》2011年第6期1109-1112,共4页Journal of Modern Oncology
基 金:云南省应用基础研究计划面上项目(编号:2007C149M);云南省教育厅科学研究基金项目(编号:07Y40515)
摘 要:目的:探讨Iressa治疗复发或转移性头颈鳞状细胞癌的疗效和安全性。方法:对接受过二线化疗方案(至少一个化疗方案包括铂类)失败的复发或转移性头颈鳞状细胞癌患者,给予Iressa每日250mg口服,持续到患者出现不可接受的不良反应或疾病进展。结果:15例患者入组,Iressa 250mg日/口服治疗能够很好耐受,只出现1级和2级不良反应,但全组无1例患者获得部分反应或全消,中位疾病进展时间为4个月,中位总生存时间为16个月。结论:Iressa能够很好耐受,但是该组患者有效率很低,它在头颈鳞状细胞癌的使用除临床研究外不推荐使用。Objective:To study the safety and initial efficacy of Iressa in patients with recurrent and metastatic head and neck squamous cell carcinomas(HNSCC) pretreated with platinum-based chemotherapy.Methods: Patients with recurrent and metastatic HNSCC who had treatment failure with at least 2 lines of chemotherapy including platinum were given Iressa at a fixed dose of 250mg daily.Treatment was continued until the patient experienced unacceptable side effects or disease progression.Results: Fifteen patients were enrolled.Treatment was well tolerated,and only grades 1 to 2 adverse events were observed.None of the patients achieved partial or complete response.Median time-to-progression was 4 months,and median overall survival was 16 months.Conclusion: Iressa was well tolerated,but the response rate was poor in this heavily pretreated study population,and its use in HNSCC is not recommended outside the context of clinical trial.
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