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因赛妥珠单抗联合西罗莫司及化疗用于治疗曲妥珠单抗治疗后PI3K/Akt/mTOR通路异常激活的HER2阳性转移性乳腺癌患者。

Inetetamab combined with sirolimus and chemotherapy for the treatment of HER2-positive metastatic breast cancer patients with abnormal activation of the PI3K/Akt/mTOR pathway after trastuzumab treatment.

作者信息

Li Qiao, Lv Dan, Sun Xiaoying, Wang Mengyuan, Cai Li, Liu Feng, Li Chenghui, Zhao Jiuda, Sun Jing, Shi Yehui, Ma Fei

机构信息

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.

Department of Medical Oncology Cancer Hospital of Huanxing Chaoyang District Beijing China.

出版信息

Cancer Innov. 2024 Sep 19;3(5):e145. doi: 10.1002/cai2.145. eCollection 2024 Oct.

Abstract

BACKGROUND

We explored the efficacy and safety of inetetamab combined with sirolimus and chemotherapy for the treatment of human epidermal factor receptor 2 (HER2)-positive metastatic breast cancer patients with abnormal activation of the PI3K/Akt/mTOR (PAM) pathway after trastuzumab treatment.

METHODS

For this prospective multicenter clinical study, HER2-positive metastatic breast cancer patients with PAM pathway mutations confirmed by histology or peripheral blood genetic testing were enrolled from July 2021 to September 2022. Patients were randomly assigned to a trial or control group. The patients in the trial group received inetetamab combined with sirolimus and chemotherapy, while the control group patients received pyrotinib and chemotherapy. The RECIST v1.1 standard was used to evaluate efficacy. Descriptive statistics were used to summarize the clinicopathological features, and the Kaplan-Meier method was used to generate survival curves. The log-rank test was used to compare progression-free survival (PFS) between the two groups.

RESULTS

A total of 59 HER2-positive metastatic breast cancer patients with abnormal activation of the PAM pathway were included, of which 37 received inetetamab combined with sirolimus and chemotherapy treatment and 22 received pyrotinib and chemotherapy treatment. The median PFS was 4.64 months in the inetetamab group and 5.69 months in the pyrotinib group, with no statistically significant difference ( = 0.507). The objective response rates were 27.3% for the inetetamab group and 29.4% for the pyrotinib group. The safety assessment indicated that the adverse event (AE) incidences were 86.1% (31/36) in the inetetamab group and 78.9 (15/19) in the pyrotinib group, with 9 (25%) and four (21.1%) Grade 3/4 AEs in the inetetamab and pyrotinib groups, respectively.

CONCLUSIONS

For metastatic HER2-positive breast cancer patients with abnormal PAM pathway activation and previous trastuzumab treatment, the combination of inetetamab with sirolimus and chemotherapy is equivalent to the combination of pyrotinib and chemotherapy. Therefore, this regimen could be a treatment option for PAM pathway-activated metastatic HER2-positive breast cancer patients.

摘要

背景

我们探讨了英特他单抗联合西罗莫司及化疗治疗曲妥珠单抗治疗后PI3K/Akt/mTOR(PAM)通路异常激活的人表皮生长因子受体2(HER2)阳性转移性乳腺癌患者的疗效和安全性。

方法

在这项前瞻性多中心临床研究中,2021年7月至2022年9月纳入经组织学或外周血基因检测确诊为PAM通路突变的HER2阳性转移性乳腺癌患者。患者被随机分配至试验组或对照组。试验组患者接受英特他单抗联合西罗莫司及化疗,而对照组患者接受吡咯替尼及化疗。采用RECIST v1.1标准评估疗效。描述性统计用于总结临床病理特征,Kaplan-Meier法用于生成生存曲线。采用对数秩检验比较两组的无进展生存期(PFS)。

结果

共纳入59例PAM通路异常激活的HER2阳性转移性乳腺癌患者,其中37例接受英特他单抗联合西罗莫司及化疗,22例接受吡咯替尼及化疗。英特他单抗组的中位PFS为4.64个月,吡咯替尼组为5.69个月,差异无统计学意义(=0.507)。英特他单抗组的客观缓解率为27.3%,吡咯替尼组为29.4%。安全性评估表明,英特他单抗组不良事件(AE)发生率为86.1%(31/36),吡咯替尼组为78.9%(15/19),英特他单抗组和吡咯替尼组3/4级AE分别有9例(25%)和4例(21.1%)。

结论

对于既往接受过曲妥珠单抗治疗且PAM通路激活异常的转移性HER2阳性乳腺癌患者,英特他单抗联合西罗莫司及化疗等同于吡咯替尼联合化疗。因此,该方案可作为PAM通路激活的转移性HER2阳性乳腺癌患者的一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f88b/11411696/5da41633feee/CAI2-3-e145-g001.jpg

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