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局部晚期乳腺癌改良根治术后多西他赛同步放化疗的放射性不良反应观察*
引用本文:陆颖,黄海欣,杨慧,陈达桂.局部晚期乳腺癌改良根治术后多西他赛同步放化疗的放射性不良反应观察*[J].中国肿瘤临床,2016,43(10):438-441.
作者姓名:陆颖  黄海欣  杨慧  陈达桂
作者单位:作者单位:广西医科大学第四附属医院肿瘤科(广西柳州市545005)
基金项目:本文课题受广西壮族自治区卫生厅自筹经费课题项目(编号z2014394)
摘    要:目的:对比观察局部晚期乳腺癌改良根治术后多西他赛同步放化疗与序贯放疗的放射性不良反应,评估多西他赛同步放化疗模式的安全性、可行性。方法:收集2009年1 月至2014年12月广西医科大学第四附属医院155 例女性乳腺癌病例,患者均行乳腺癌改良根治术,病理诊断为乳腺浸润性导管癌,TNM 分期为pT3~4pN1~3cM0 或p 任意TpN 2~3cM0。采用氟尿嘧啶+ 表柔比星+ 环磷酰胺(FEC )化疗方案后,密闭信封法随机分为同步组(多西他赛化疗时同步放疗)78例、序贯组(多西他赛化疗完成后放疗)77例,观察两组放射性不良反应及近期疗效。结果:中位随访39(16~62)个月。同步组和序贯组的放射性不良反应轻微,均无3~4 级放射性皮肤反应、症状性心肺放射损伤。1~2 级放射性皮肤反应同步组的发生率为89.7%(70/ 78)、序贯组为88.3%(68/ 77),两组比较差异无统计学意义(P > 0.05)。 3 年无复发生存率同步组为92.3%(72/ 78),序贯组为81.8%(63/ 77),两组比较差异具有统计学意义(P = 0.046)。 结论:局部晚期乳腺癌改良根治术后多西他赛同步放化疗的放射性不良反应轻微,与序贯治疗比较提高了患者的3 年无复发生存率,安全可行,可作为局部晚期乳腺癌的治疗选择。 

关 键 词:乳腺肿瘤?    乳房切除术?    改良根治性    化学疗法?    放射疗法?    辅助
收稿时间:2016-02-01

Adverse reactions of chemoradiotherapy with docetaxel after modified radical mastectomy in locally advanced breast cancer
Institution:This work was supported by the Self-financing Project from the Department of Health of Guangxi Zhuang Autonomous Region (No. z2014394)
Abstract:Objective:To compare the adverse reactions of concurrent chemoradiotherapy with docetaxel versus those of sequential and scheduled adjuvant therapy after a modified radical mastectomy in locally advanced breast cancer. Additionally, this work aims to evaluate the safety and feasibility of a synchronous therapy schedule. Methods:A total of 155 female breast cancer patients in the Fourth Affiliated Hospital of Guangxi Medical University were enrol ed from January 2009 to December 2014. Al the patients were diagnosed with infiltrating ductal carcinoma and stage pT3-4, pN1-3c M0, or pAnyTpN2-3cM0 after modified radical mastectomy. After completing the fluorouracil+epirubicin+cyclophosphamide adjuvant chemotherapy, all the patients were randomly divided into two groups by using the method of sealed envelopes. The synchronous group, which received synchronous chemoradiotherapy with docetaxel, comprised 78 cases. The sequential group, which received radiotherapy fol owing docetaxel chemotherapy, comprised 77 cases. The clinical toxic reactions and effects in both groups were assessed after all schedules. Results:A median follow-up period of 39 (16-62) months showed that the radiation side effects of the synchronous and sequential groups were mild. No patients with 3-4 grade radiation-induced skin reactions or symptoms of heart and lung radiation side effects were reported. The rate of 1-2 grade radiation-induced skin reactions was 89.7%(70/78) in the synchronous group and 88.3%(68/77) in the sequential group, but the difference was not statistically significant (P>0.05). The three-year recurrence-free survival rate was 92.3%(72/78) in the synchronous group and 81.8%(63/77) in the sequential group, and the difference was statistically significant (P=0.046). Conclusion:Synchronous chemoradiotherapy with docetaxel as adjuvant therapy exhibited mild and tolerable adverse reactions fol owing modified radical mastectomy in local y advanced breast cancer. Compared with the sequential schedule, the synchronous schedule showed a significantly increased three-year recurrence-free survival rate. Therefore, a synchronous chemo-radiotherapy schedule is safe and feasible and can be used as a treatment option for locally advanced breast cancer.
Keywords:breast neoplasms  mastectomy  modified radical  chemotherapy  radiotherapy  adjuvant
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