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中华养生保健 ›› 2023, Vol. 41 ›› Issue (3): 45-48.

• 临床研究 • 上一篇    下一篇

多西他赛联用不同抗肿瘤药物用于乳腺癌的不良反应分析及临床用药评价

黄晓婷1, 郭岱年2, 方翎1, 张汉增3,*   

  1. 1.汕头大学医学院附属肿瘤医院药学部,广东 汕头,515000;
    2.汕头大学医学院附属肿瘤医院临床药物试验机构,广东 汕头,515000;
    3.汕头大学医学院附属肿瘤医院静配中心,广东 汕头,515000
  • 出版日期:2023-02-01 发布日期:2023-02-06
  • 通讯作者: * 张汉增,E-mail:3238218317@qq.com。
  • 作者简介:黄晓婷(1992—),女,汉族,籍贯:广东省汕头市,本科,药师,研究方向:肿瘤药学。

Adverse Reaction Analysis and Clinical Evaluation of Docetaxel Combined with Different Antineoplastic Drugs in Breast Cancer

HUANG Xiao-ting1, GUO Dai-nian2, FANG Ling1, ZHANG Han-zeng3,*   

  1. 1. Department of Pharmacy, Affiliated Cancer Hospital of Shantou University School of Medicine, Shantou Guangdong 515000, China;
    2. Clinical Drug Trials, Affiliated Cancer Hospital of Shantou University School of Medicine, Shantou Guangdong, 515000, China;
    3. Intravenous Center, Affiliated Cancer Hospital of Shantou University School of Medicine, Shantou Guangdong, 515000, China
  • Online:2023-02-01 Published:2023-02-06

摘要: 目的 探讨多西他赛联用不同抗肿瘤药物用于乳腺癌的不良反应分析及临床用药评价。方法 采用回顾性研究选取2020年3月—2021年3月在汕头大学医学院附属肿瘤医院就诊的78例乳腺癌患者,根据治疗方案不同分为三组,TH(多西他赛+曲妥珠单抗)组24例,TE(多西他赛+表柔比星)组25例,TEC(多西他赛+表柔比星+环磷酰胺)组29例。对比三组临床疗效、不良反应、血清生化指标和1年生存率。结果 TH组疗效显著高于TE组,差异有统计学意义(P<0.05);TEC组疗效显著高于TE组,差异有统计学意义(P<0.05);TH组和TEC组疗效比较,差异无统计学意义(P>0.05)。三组不良反应均为轻度,三组不良反应比较,差异无统计学意义(P>0.05)。三组可溶性自杀相关因子(sFas)水平和1年生存率比较,差异有统计学意义(P<0.05),其中sFas水平两两组间比较,差异有统计学意义(P<0.05),TEC组1年生存率显著高于TE组,差异有统计学意义(P<0.05),其余两两组间1年生存率比较,差异无统计学意义(P>0.05)。三组促卵泡生长激素(FSH)和雌二醇(E2)比较,差异无统计学意义(P>0.05)。结论 多西他赛联合曲妥珠单抗与多西他赛联合表柔比星和环磷酰胺治疗乳腺癌效果和安全性相当,均优于多西他赛与表柔比星,且多西他赛联合表柔比星和环磷酰胺在抑制肿瘤细胞增殖方面效果最好,生存率高于多西他赛与表柔比星,临床中可根据患者情况酌情选择。

关键词: 乳腺癌, 多西他赛, 曲妥珠单抗, 表柔比星, 环磷酰胺

Abstract: Objective To investigate the adverse reaction analysis and clinical evaluation of docetaxel combined with different antineoplastic drugs in breast cancer. Methods A retrospective study was conducted to select 78 breast cancer patients from March 2020 to March 2021 in the Affiliated Cancer Hospital of Shantou University Medical College. According to different treatment schemes, they were divided into three groups: TH (Docetaxel+Trastuzumab) group with 24 cases, TE (Docetaxel+Epirubicin) group with 25 cases, and TEC (Docetaxel+Epirubicin+Cyclophosphamide) group with 29 cases. The clinical efficacy, adverse reactions, serum biochemical index and 1-year survival rate of the three groups were compared. Results The therapeutic of TH group was significantly higher than that of TE group (P<0.05); the therapeutic of TEC group was significantly higher than that of TE group (P<0.05); the difference of curative effect between TH group and TEC group was not statistically significant (P>0.05). The adverse reactions of the three groups were mild, and there was no significant difference among the three groups (P>0.05). Compared with the 1-year survival rate of the three groups, the differences were statistically significant (P<0.05), among which the differences were statistically significant (P<0.05). The 1-year survival rate of TEC group was significantly higher than that of TE group (P<0.05), but there was no statistical difference between the other two groups (P>0.05). There was no significant difference in FSH and E2 between the three groups (P>0.05). Conclusion The efficacy and safety of Docetaxel combined with Trastuzumab is similar to that of Docetaxel combined with Epirubicin and Cyclophosphamide in the treatment of breast cancer, both of which are superior to those of Docetaxel and Epirubicin. Moreover, Docetaxel combined with Epirubicin and Cyclophosphamide has the best effect in inhibiting tumor cell proliferation, and the survival rate is higher than that of Docetaxel and Epirubicin, which can be selected according to the patient's condition.

Key words: breast cancer, docetaxel, trastuzumab, epirubicin, cyclophosphamide

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