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作 者:毕益明[1] 付艳[1] 陈秀芳[1] 郑东星[1] 李强[1] 张素美[1] 王淑燕[1]
机构地区:[1]山东省滨州市人民医院肿瘤二科,山东滨州256610
出 处:《现代肿瘤医学》2010年第10期1970-1972,共3页Journal of Modern Oncology
摘 要:目的:观察吉西他滨联合卡培他滨治疗难治性乳腺癌的疗效和不良反应。方法:37例难治性乳腺癌患者,应用吉西他滨联合卡培他滨,持续应用至疾病进展或出现不能耐受的不良反应。并按WHO标准评价疗效及不良反应,随访生存情况。结果:在37例可评价的患者中,CR 3例,PR 12例,SD 13例,PD 9例。RR为40.54%;DCR为75.68%。中位TTP为9个月(95%CI:6.115-11.885M);中位OS为15个月(95%CI:10.663-19.337M)。主要不良反应为骨髓抑制,其次为胃肠道反应。结论:吉西他滨联合卡培他滨治疗难治性乳腺癌有较好的疗效,不良反应可以耐受。Objective:To evaluate the efficacy and side effects of gemcitabine plus capecitabine for refractory patients with metastatic breast cancer.Methods:Thirty-seven patients with metastatic breast cancer were treated by gemcitabine plus capecitabine.Response and side effect were evaluated by WHO standard.Results:Among 37 patients,3 cases achieved CR,12 PR,13 SD,9 PD.The remission rate was 40.54%,and total disease control rate was 75.68%,median time to progression was 9(95%CI:6.115-11.885)months and median overall survival time was 15(95%CI:10.663-19.337)months.The major adverse events were bone marrow suppression and gastrointestinal side effect.Conclusion:Gemcitabine plus capecitabine is an effective and well tolerate regimen for refractory patients with metastatic breast cancer.
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