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:朱跃红[1] 罗以[1] 杨农[1] 吴尉[1] 林劲冠[1] 杨挚鹰[2]
机构地区:[1]湖南省肿瘤医院,410013 [2]湖南师范大学医学院,410013
出 处:《实用癌症杂志》2009年第2期158-161,共4页The Practical Journal of Cancer
基 金:湖南省教育厅科学研究项目(07C568)
摘 要:目的探讨紫杉醇联合蒽环类药物±CTX方案与CAF方案治疗晚期乳腺癌的近期临床疗效和不良反应。方法以紫杉醇联合蒽环类药物±CTX方案为观察组,CAF方案为对照组。结果观察组有效率为72.7%(16/22),对照组为53.8%(14/26),观察组优于对照组,但无显著性差异(P>0.05)。年龄,月经状况,ER、PR,基因表达,临床分期,远处转移等因素,对近期疗效无显著影响(P>0.05)。不良反应以白细胞减少为主,观察组Ⅲ-Ⅳ度发生率为59.1%,对照组为11.5%,两组比较有显著性差异(P<0.01),其他与化疗相关的不良反应程度均较轻,可耐受。结论对于晚期乳腺癌初用化疗者,CAF组与观察组相比疗效无显著差异且不良反应较轻,临床更具优势,值得临床广泛应用。Objective To study the short-term efficacy and toxicities of combined paclitaxel plus antracycline ± CTX and CAF treatment for advanced breast cancer. Methods Patients treated with paclitaxel plus antraeycline ± CTX were included in the study group, and patients treated with the CAF were included in the control group. Results The response rate was 72.7 % (16/22) for the study group, and 53.8% (14/26) for the control group, with no significant differences ( P 〉 0. 05 ). Age, menstruation status, ER, PR, gene expression, clinical TNM stage and distant metastases had no significant correlations with the shortteim clinical efficacy (P 〉0.05). The major toxicity was leucopenia,with 59.1% and 11.5% patients having III-1V leucopenia in the study and control group, respectively. This difference was statistically significant ( P 〈 0.01 ). Other chemotherapy-related toxicities were mild and tolerable. Conclusion CAF chemotherapy has the same efficacy as the paclitaxel plus antracyeline ± CTX regime, but with less toxicities,in the treatment of patients with advanced breast cancer.
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:216.73.216.229