临床和实验医学杂志2024,Vol.23Issue(3) :270-274.DOI:10.3969/j.issn.1671-4695.2024.03.012

帕妥珠单抗联合含蒽环类化疗方案新辅助治疗HER2阳性乳腺癌的获益与安全性

Benefit and safety of new adjuvant treatment of HER2 positive breast cancer with patuzumab combined with anthracycline chemothera-py

梁朝晖 杜巧红
临床和实验医学杂志2024,Vol.23Issue(3) :270-274.DOI:10.3969/j.issn.1671-4695.2024.03.012

帕妥珠单抗联合含蒽环类化疗方案新辅助治疗HER2阳性乳腺癌的获益与安全性

Benefit and safety of new adjuvant treatment of HER2 positive breast cancer with patuzumab combined with anthracycline chemothera-py

梁朝晖 1杜巧红1
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作者信息

  • 1. 运城市中心医院放疗科 山西 运城 044000
  • 折叠

摘要

目的 探究帕妥珠单抗联合含蒽环类化疗方案新辅助治疗人表皮生长因子受体2(HER2)阳性乳腺癌的获益与安全性.方法 前瞻性选取2021年5月至2022年5月在运城市中心医院进行治疗的HER2阳性乳腺癌患者486例纳入本研究,按照随机数字表法将患者分为对照组(n=243)和研究组(n=243).对照组接受传统含蒽环类化疗方案,研究组接受帕妥珠单抗联合含蒽环类化疗方案新辅助化疗,两组化疗后均接受手术治疗.比较两组疗效,检测并记录两组治疗前后肿瘤标志物[癌胚抗原、癌抗原(CA)125、CA153]水平,并记录两组不良反应发生情况和预后情况.结果 研究组的治疗总有效率为90.12%,高于对照组(76.15%),差异有统计学意义(P<0.05).治疗后,两组患者的癌胚抗原、CA125、CA153水平均较治疗前有所下降,差异均有统计学意义(P<0.05);研究组的癌胚抗原水平为(1.89 ±0.78)pg/mL,低于对照组[(1.89±0.78)pg/mL],差异有统计学意义(P<0.05),但两组间的CA125、CA153水平比较,差异均无统计学意义(P>0.05).两组不良反应发生情况比较,差异无统计学意义(P>0.05).研究组的复发率、转移率、病死率及总预后不良率分别为4.94%、6.58%、10.70%、22.22%,均低于对照组(10.29%、13.58%、22.63%、46.50%),差异均有统计学意义(P<0.05).结论 帕妥珠单抗联合含蒽环类化疗方案新辅助治疗HER2阳性乳腺癌患者是一种有效、安全的治疗方案.其可提高治疗有效率,且不会给患者带来额外的不良反应,改善患者的预后情况.

Abstract

Objective To explore the benefit and safety of the neoadjuvant treatment of human epidermal growth factor receptor 2(HER2)positive breast cancer with patuzumab combined with anthracycline chemotherapy.Methods A total of 486 HER2 positive breast cancer patients who admitted,in Yuncheng Central Hospital from January 2021 to January 2022 were prospectively selected and divided into two groups:the con-trol group(n=243)and the study group(n=243)according to the random number table method.The control group received the traditional anthracycline containing chemotherapy scheme,and the study group received the neoadjuvant chemotherapy of patuzumab combined with anthracy-cline containing chemotherapy scheme.The therapeutic effects of two groups were compared,and the levels of tumor markers[carcinoembryonic antigen,cancer antigen(CA)125,CA153]were detected and recorded before and after treatment in two groups.Adverse reactions and prognosis were also recorded in two groups.Results The total effective rate of treatment in the research group was 90.12%,which was higher than that in the control group(76.15%),and the difference was statistically significant(P<0.05).After treatment,the levels of carcinoembryonic anti-gen,CA125,and CA153 in two groups of patients were lower than those before treatment,and the differences were statistically significant(P<0.05);the level of carcinoembryonic antigen in the study group was(1.89±0.78)pg/mL,which was lower than that in the control group[(1.89±0.78)pg/mL],and the difference was statistically significant(P<0.05).However,there were no statistically significant differences in the levels of CA125 and CA153 between the two groups(P>0.05).There was no statistically significant difference in the incidence of adverse reactions between the two groups(P>0.05).The recurrence rate,metastasis rate,mortality rate,and overall poor prognosis rate of the study group were 4.94%,6.58%,10.70%,and 22.22%,respectively,which were lower than those of the control group(10.29%,13.58%,22.63%,and 46.50%),and the differences were statistically significant(P<0.05).Conclusion Pertuzumab combined with anthracycline-containing chemotherapy is an effective and safe neoadjuvant therapy for HER2-positive breast cancer patients.It can improve the effective rate of treatment,and will not bring additional adverse reactions to patients,improve the prognosis of patients.

关键词

抗体,单克隆/蒽环类/乳腺癌/帕妥珠单抗/含蒽环类化疗方案/HER2阳性乳腺癌/安全性

Key words

Antibodies,monoclonal/Anthracyclines/Breast cancer/Patuzumab/Anthracycline containing chemotherapy regimen/HER2 positive breast cancer/Safety

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基金项目

山西省卫生健康委科研项目(2019163)

出版年

2024
临床和实验医学杂志
首都医科大学附属北京友谊医院

临床和实验医学杂志

CSTPCD
影响因子:1.504
ISSN:1671-4695
参考文献量20
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