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曲妥珠单抗德鲁昔单抗在中国HER2阳性和HER2低表达晚期乳腺癌患者中的疗效和安全性:一项多中心、观察性、真实世界研究。

Efficacy and safety of trastuzumab deruxtecan in Chinese patients with HER2-positive and HER2-low advanced breast cancer: a multicenter, observational, real-world study.

作者信息

Sang Die, Su Yanfang, Zhang Yurong, Guan Yanfeng, Fan Shanmin, Zhang Jintao, Zheng Lijun, Wang Yanling, Guo Ying, Lei Zixuan, Li Man, Yuan Peng

机构信息

Department of Oncology, The Second Hospital of Dalian Medical University, Dalian, China.

Department of Medical Oncology, Beijing Chaoyang District Sanhuan Cancer Hospital, Beijing, China.

出版信息

Ther Adv Med Oncol. 2025 Feb 28;17:17588359251318853. doi: 10.1177/17588359251318853. eCollection 2025.

Abstract

OBJECTIVE

Limited real-world efficacy and safety data exist regarding the use of trastuzumab deruxtecan (T-DXd) in the Chinese population with human epidermal growth factor receptor (HER2)-positive and HER2-low advanced breast cancer (BC). This multicenter, observational, real-world study aimed to evaluate the efficacy and safety of T-DXd for the treatment of Chinese patients with HER2-positive and HER2-low advanced BC.

METHODS

The medical records of 61 patients were collected from The Second Hospital of Dalian Medical University, Beijing Chaoyang District Sanhuan Cancer Hospital, Beijing Jingxin Hospital, and Cancer Hospital of the Chinese Academy of Medical Sciences. The primary endpoint of the study was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), time to response (TTR), and safety. PFS and OS were analyzed using the Kaplan-Meier method and log-rank test.

RESULTS

The primary endpoint, PFS was 10.51 months (95% confidence interval (CI), 3.02-NE) in the HER2-low group and 10.18 months (95% CI, 3.88-NE) in the HER2-positive group. Regarding the secondary endpoints in the HER2-low and HER2-positive groups, OS data were immature, ORR rates were 37.93% and 62.50%, DCR rates were 79.31% and 87.50%, and the median TTR rates were 1.28 and 1.31 months, respectively. In the subgroup analysis, front-line treatment with T-DXd was associated with increased beneficial effects. The primary adverse events (AEs) related to T-DXd treatment were gastrointestinal reactions and bone marrow suppression, which were predominantly grades 1-2, with no severe grade 4/5 AEs reported, only one patient developed infectious pneumonia.

CONCLUSION

This study was the first multicenter, real-world study of T-DXd for advanced BC in China. The findings demonstrated that T-DXd may be an effective antitumor treatment with controllable adverse reactions in patients with advanced BC irrespective of HER2 expression levels.

摘要

目的

关于曲妥珠单抗德鲁替康(T-DXd)在中国表皮生长因子受体(HER2)阳性和HER2低表达的晚期乳腺癌(BC)患者中的应用,现有的真实世界疗效和安全性数据有限。这项多中心、观察性的真实世界研究旨在评估T-DXd治疗中国HER2阳性和HER2低表达晚期BC患者的疗效和安全性。

方法

收集大连医科大学附属第二医院、北京朝阳区三环肿瘤医院、北京京新医院和中国医学科学院肿瘤医院61例患者的病历。该研究的主要终点是无进展生存期(PFS),次要终点是总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)、缓解时间(TTR)和安全性。采用Kaplan-Meier法和对数秩检验分析PFS和OS。

结果

HER2低表达组的主要终点PFS为10.51个月(95%置信区间(CI),3.02-未达到),HER2阳性组为10.18个月(95%CI,3.88-未达到)。关于HER2低表达和HER2阳性组的次要终点,OS数据不成熟,ORR率分别为37.93%和62.50%,DCR率分别为79.31%和87.50%,中位TTR率分别为1.28和1.31个月。在亚组分析中,T-DXd一线治疗与疗效增加相关。与T-DXd治疗相关的主要不良事件(AE)是胃肠道反应和骨髓抑制,主要为1-2级,未报告严重的4/5级AE,仅1例患者发生感染性肺炎。

结论

本研究是中国首个关于T-DXd治疗晚期BC的多中心真实世界研究。研究结果表明,无论HER2表达水平如何,T-DXd对于晚期BC患者可能是一种有效的抗肿瘤治疗方法,且不良反应可控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/11873904/70a04a0b822e/10.1177_17588359251318853-fig1.jpg

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