曲妥珠单抗德鲁司替康治疗her2阳性和her2低转移性乳腺癌的疗效:一项中国真实世界回顾性队列研究

IF 3.4 4区 医学 Q2 ONCOLOGY
Breast Cancer : Targets and Therapy Pub Date : 2025-09-25 eCollection Date: 2025-01-01 DOI:10.2147/BCTT.S545308
Yuxin Yan, Yizi Jin, Mingxi Lin, Ceng Zeng, Qing Guo, Teng Zhou, Dou Dou Li, Jian Zhang
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引用次数: 0

摘要

背景:关于曲妥珠单抗德鲁西替康(T-DXd, DS8201a)在her2阳性和her2低转移性乳腺癌(MBC)患者中的有效性和安全性的真实数据有限,特别是在中国人群中。方法:回顾性分析2022 - 2025年复旦大学上海肿瘤中心接受T-DXd治疗的98例MBC患者。患者分为her2阳性组和her2低组。临床结果包括客观缓解率(ORR)、无进展生存期(PFS)、疾病控制率(DCR)和临床获益率(CBR)进行评估和比较。研究的主要终点是PFS,使用Kaplan-Meier方法估计PFS,并使用Log rank检验进行比较。结果:98例患者中位PFS为15.0个月。ORR、DCR、CBR分别为48.0%、69.4%、41.8%。her2阳性患者比her2低患者有更长的PFS(未达到vs 9.0个月)。在her2低的患者中,肝转移与较差的预后相关。脑转移患者的中位PFS为15.5个月,1年PFS率为65.3%。≥3级不良事件包括中性粒细胞减少症(20.4%)、恶心(5.1%)、贫血(4.1%)和间质性肺疾病(6.1%),导致2.0%的患者停药。结论:在这项现实世界的分析中,T-DXd在her2阳性和her2低水平的MBC中都表现出强大的临床活性,与DESTINY-Breast临床试验的结果一致。值得注意的是,我们确定了几个临床相关的预后因素,包括HER2状态、转移部位、治疗线和既往治疗。这些发现支持了T-DXd更广泛的临床应用,并为个体化治疗选择提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of Trastuzumab Deruxtecan in HER2-Positive and HER2-Low Metastatic Breast Cancer: A Real-World Retrospective Cohort Study in China.

Efficacy of Trastuzumab Deruxtecan in HER2-Positive and HER2-Low Metastatic Breast Cancer: A Real-World Retrospective Cohort Study in China.

Efficacy of Trastuzumab Deruxtecan in HER2-Positive and HER2-Low Metastatic Breast Cancer: A Real-World Retrospective Cohort Study in China.

Efficacy of Trastuzumab Deruxtecan in HER2-Positive and HER2-Low Metastatic Breast Cancer: A Real-World Retrospective Cohort Study in China.

Background: Limited real-world data are available on the effectiveness and safety of trastuzumab deruxtecan (T-DXd, DS8201a) in patients with HER2-positive and HER2-low metastatic breast cancer (MBC), particularly within the Chinese population.

Methods: Between 2022 and 2025, 98 patients with MBC treated with T-DXd were retrospectively enrolled at Fudan University Shanghai Cancer Center. Patients were categorized as HER2-positive and HER2-low cohort. Clinical outcomes including objective response rate (ORR), progression-free survival (PFS), disease control rate (DCR), and clinical benefit rate (CBR), were assessed and compared between cohorts. The primary endpoint of the study was PFS, which was estimated using the Kaplan-Meier method and compared using the Log rank test.

Results: Among the 98 patients, the median PFS was 15.0 months. The ORR, DCR, and CBR were 48.0%, 69.4%, and 41.8%, respectively. HER2-positive patients experienced longer PFS compared to HER2-low patients (not reached vs 9.0 months). Among HER2-low patients, liver metastases were associated with poorer outcomes. Patients with brain metastases achieved a median PFS of 15.5 months and a 1-year PFS rate of 65.3%. Grade ≥3 adverse events included neutropenia (20.4%), nausea (5.1%), anemia (4.1%), and interstitial lung disease in 6.1% of patients, leading to discontinuation in 2.0%.

Conclusion: In this real-world analysis, T-DXd demonstrated robust clinical activity in both HER2-positive and HER2-low MBC, consistent with the findings from the DESTINY-Breast clinical trials. Notably, we identified several clinically relevant prognostic factors, including HER2 status, metastatic site, treatment line, and prior therapies. These findings support the broader clinical application of T-DXd and offer insights into individualized treatment selection.

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来源期刊
CiteScore
4.10
自引率
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审稿时长
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