检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:毕书婷[1]
机构地区:[1]南京市胸科医院呼吸科二病区,江苏南京210029
出 处:《中国现代医生》2009年第36期54-55,97,共3页China Modern Doctor
摘 要:目的对培美曲塞联合顺铂治疗晚期非小细胞肺癌(NSCLC)进行临床疗效和毒性评价。方法45例经病理组织学和/或细胞学检查确诊NSCLC,均为初治患者,其中男性28例,女性17例;年龄31~76岁,中位年龄58岁,鳞癌12例,腺癌30例,腺鳞癌3例,TNM分期:ⅢA7例,ⅢB16例,Ⅳ22例,应用培美曲塞联合顺铂治疗,即培美曲塞500mg/m2,顺铂75mg/m2,21d为一周期,至少接受2个周期化疗。按照WHO标准评价临床疗效和毒性。结果45例患者中,无完全缓解(CR)病例,部分缓解(PR)10例,稳定(SD)13例,进展(PD)22例,有效率(CR+PR)22.22%,临床获益率(CR+PR+SD)51.11%,主要毒性反应为骨髓抑制,胃肠道反应。结论培美曲塞联合顺铂治疗晚期NSCLC疗效可靠,毒性反应小,与国内外文献报道的缓解率及有效率类似。Objective To observe the clinical efficacy and adverse effects of peme/rexed combined with oxaliplatin to treat advanced non-small cell lung cancer. Methods Forty-five cases aged 31-76 years(a median age of 58 years were newly diagnosed as advanced non-small cell lung cancer by histopathological and/or cytology,28 cases were male and 17 female,and in 45 cases, 12 cases were squamous cell carcinoma, 30 were adenocarcinoma and 3 were adenosquamous carcinoma. TNM staging showed 7 cases of Ⅲ A, 16 cases of Ⅲ B and 22cases of Dr. Pemetrexed 500mg/m^2 and cisplatin 75mg/m^2 were used for at least 2 cycles of chemotherapy with 21 days as a cycle. Based on WHO criteria,the clinical efficacy and toxicity weir evaluated. Results In 45 patients, there were no cases of complete remission (CR), 10 cases of partial remission(PR)13 cases of stablility(SD)and 22 cases of progTess(PD). The effective rate( CR+PR )was 22.22% and the clinical benefit rate(CR+PR+SD) was 51.11%,and the main side effects were myelosuppression and gastrointestinal tract reaction. Conclusion The combination of pemetrexed and oxaliplatin in the treatment of advanced non-small cell lung cancer has reliable efficacy and fewer side effects, showing similar remission rate and effective rate reported in the literature at home and abroad.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.97