首页|伊尼妥单抗治疗晚期乳腺癌的真实世界研究

伊尼妥单抗治疗晚期乳腺癌的真实世界研究

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目的 观察真实世界中伊尼妥单抗治疗晚期乳腺癌的疗效和安全性.方法 回顾性分析 2020 年 8 月至2022 年 8 月就诊于襄阳市中心医院并接受伊尼妥单抗治疗的 63 例晚期乳腺癌患者的临床资料.生存分析采用Kaplan-Meier法绘制生存曲线并进行Log-rank检验,采用Cox比例风险回归模型分析影响预后的危险因素,采用非参数检验Kruskal-Wallis分析不同亚组间治疗疗效的差异.结果 63 例患者的客观缓解率(ORR)为 47.6%(30/63),疾病控制率(DCR)为 66.7%(42/63).伊尼妥单抗一线至二线治疗患者的ORR、DCR分别为 85.0%、90.0%,三线至七线治疗患者的ORR、DCR分别为30.2%、55.8%,两组比较差异有统计学意义(P<0.05).既往使用过曲妥珠单抗和酪氨酸激酶抑制剂(TKI)药物的患者ORR、DCR分别为 31.0%、54.8%,既往未使用过曲妥珠单抗和TKI药物的患者ORR、DCR分别为 81.0%、90.5%,两组比较差异有统计学意义(P<0.05).全体患者的中位无进展生存期(PFS)为 5 个月.单因素分析显示,伊尼妥单抗治疗线数、转移部位数、既往曲妥珠单抗和TKI药物使用情况及近期疗效均与患者预后有关(P<0.05).多因素Cox回归分析显示,近期疗效是影响患者预后的独立因素(P<0.05).3~4 级不良反应的发生率为 9.5%(6/63),其中血小板减少 1 例、贫血 1 例、肾功能不全2 例、腹泻 2 例.结论 伊尼妥单抗治疗晚期乳腺癌疗效确切,不良反应可控,具有较好的临床应用价值.
A real-world study on the efficacy and safety of inetetamab in the treatment of advanced breast cancer
Objective To observe the efficacy and safety of inetetamab in the treatment of advanced breast cancer in the real-world.Methods A retrospective analysis was performed on 63 patients with advanced breast cancer admitted to Xiangyang Central Hospital from August 2020 to August 2022.Survival curve was plotted by Kaplan-Meier method and performed with Log-rank test.Cox proportional risk model was used to analyze the risk factors affecting the prognosis,and non-parametric test Kruskal-Wallis was used to analyze the difference in treatment efficacy among different subgroups.Results The objective response rate(ORR)of 63 patients was 47.6%(30/63),and the disease control rate(DCR)was 66.7%(42/63).The ORR and DCR of the patients treated with first-line and second-line inetetamab were 85.0%and 90.0%,and those treated with third-line to seventh-line inetetamab were 30.2%and 55.8%,respectively,and the difference between the two groups was statistically significant(P<0.05).The ORR and DCR of patients who had previously used trastuzumab and tyrosine kinase inhibitor(TKI)were 31.0%and 54.8%,respectively,and those who had not used trastuzumab and TKI before were 81.0%and 90.5%,respectively,and the difference between the two groups was statistically significant(P<0.05).The median progression-free survival(PFS)for all patients was 5 months.Univariate analysis showed that the number of treatment lines,number of metastatic sites,previous use of trastuzumab and TKI drugs,and efficacy were all related to prognosis(P<0.05).Multivariate analysis showed that efficacy evaluation was an independent prognostic factor(P<0.05).The incidence of grade 3-4 adverse reactions was 9.5%(6/63),including 1 case of thrombocytopenia,1 case of anemia,2 cases of renal insufficiency,and 2 cases of diarrhea.Conclusion The efficacy of inetetamab in the treatment of advanced breast cancer is definite,and the adverse reactions are controllable,which has good clinical application value.

Breast neoplasmsInetetamabEfficacySafety

关格格、刘晖杰、孙秋实、王越华、陈德杰

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441021 湖北襄阳 湖北文理学院附属医院 襄阳市中心医院肿瘤科

441021 湖北文理学院附属医院 襄阳市中心医院普外科

乳腺肿瘤 伊尼妥单抗 疗效 安全性

中国抗癌协会HER-2靶点中国科研基金

CORP-239-S8

2024

临床肿瘤学杂志
解放军第八一医院

临床肿瘤学杂志

CSTPCD
影响因子:1.583
ISSN:1009-0460
年,卷(期):2024.29(2)
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