临床外科杂志 ›› 2023, Vol. 31 ›› Issue (11): 1061-1064.doi: 10.3969/j.issn.1005-6483.2023.11.016

• 论著 • 上一篇    下一篇

拉帕替尼联合曲妥珠单抗治疗人表皮生长因子受体2阳性乳腺癌病人的疗效及生存预后分析

  

  1. 130012  长春,吉林省肿瘤医院肿瘤内一科
  • 收稿日期:2022-10-09 修回日期:2022-10-09 接受日期:2022-10-09 出版日期:2023-11-20 发布日期:2023-11-20
  • 通讯作者: 牛凯,Email:niukai20221020@163.com

Efficacy of lapatinib combined with trastuzumab on patients with HER2-positive breast cancer and analysis of survival prognosis

  1. Department of Oncology,Jilin Cancer Hospital,Changchun 130012,China
  • Received:2022-10-09 Revised:2022-10-09 Accepted:2022-10-09 Online:2023-11-20 Published:2023-11-20

摘要: 目的 探究拉帕替尼联合曲妥珠单抗治疗人表皮生长因子受体2(HER2)阳性乳腺癌病人的疗效及对生存预后的影响。方法 2016年4月~2018年6月行新辅助化疗治疗的HER2阳性乳腺癌病人86例,采用随机数字表法将其分为观察组(拉帕替尼联合曲妥珠单抗治疗)及对照组(曲妥珠单抗治疗),每组各43例。比较两组治疗疗效,记录病人治疗前后血管内皮生长因子、炎性因子及凋亡因子水平变化;所有病人均随访3年或随访至其死亡,比较两组病人累积生存率,统计治疗期间不良事件发生情况。结果 观察组、对照组客观缓解率、疾病控制率分别为72.09%、86.07% 和58.14%、74.42%,两组比较差异无统计学意义(P>0.05);观察组治疗后血管内皮生长因子A、血管内皮生长因子B、血管内皮生长因子C及肿瘤坏死因子α、白细胞介素(IL-1β、IL-6、IL-8水平低于对照组,治疗后诱骗受体3及环氧化酶-2表达量低于对照组,两组比较差异有统计学意义(P<0.05);观察组、对照组3年生存率分别为46.51%(20/43)、30.23%(13/43),中位生存时间为34.5个月、26.7个月,两组比较差异无统计学意义(P>0.05);两组不良事件发生率比较,差异无统计学意义(P>0.05)。结论 拉帕替尼联合曲妥珠单抗治疗HER2阳性乳腺癌病人,可降低血管内皮因子及炎症因子水平,抑制凋亡因子释放,但对3年生存率影响不大。

关键词: 拉帕替尼, 曲妥珠单抗, 人表皮生长因子受体2, 乳腺癌, 生存

Abstract: Objective To explore the efficacy of lapatinib combined with trastuzumab in the treatment of patients with human epidermal growth factor receptor-2 (HER2)-positive breast cancer and its effects on survival prognosis.Methods 86 patients with HER2-positive breast cancer who were treated with neoadjuvant chemotherapy from April 2016 to June 2018 were selected as the research subjects,and they were divided into observation group (lapatinib combined with trastuzumab treatment) and control group (trastuzumab treatment) by means of the random number table method,with 43 cases in each group.The therapeutic efficacy of the two groups was compared,and the changes in levels of vascular endothelial growth factor,inflammatory factors and apoptotic factors were recorded before and after treatment.All patients were followed up for 3 years or until their death,and the cumulative survival rate was compared between the two groups,and the occurrence of adverse events during treatment were counted.Results There were no significant differences in objective response rate (ORR) and disease control rate (DCR) between observation group and control group (72.09% vs 58.14%,86.07% vs 74.42%,P>0.05).After treatment,the levels of vascular endothelial growth factor A (VEGFA),vascular endothelial growth factor B (VEGFB),vascular endothelial growth factor C (VEGFC),tumor necrosis factor-α (TNFα),interleukin-1β (IL-1β),interleukin-6 (IL-6) and interleukin-8 (IL-8) in observation group were lower than those in control group,and the expression levels of decoy receptor 3 (DcR3) and cyclooxygenase-2 (COX-2) after treatment were also lower than those in control group (P<0.05).The 3 year survival rates in observation group and control group were 46.51% (20/43) and 30.23% (13/43),and the median survival times were 34.5 months and 26.7 months (P>0.05).There were no significant differences between the two groups in terms of incidence rates of adverse events (P>0.05).Conclusion Lapatinib combined with trastuzumab in the treatment of patients with HER2-positive breast cancer can reduce the levels of vascular endothelial factors and inflammatory factors and inhibit the releases of apoptotic factors,but has little effect on the 3-year survival rate of patients.

Key words: lapatinib, trastuzumab, human epidermal growth factor receptor-2 positive, breast cancer, survival

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