中国转移性乳腺癌患者T-DXd治疗的真实多中心研究

IF 7.6 1区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Biyun Wang , Yumeng Li , Yannan Zhao , Die Sang , Peng Yuan , Yanxia Zhao , Zheng Lv , Ning Xie , Nanling Li , Juanjuan Li , Fang Wang
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引用次数: 0

摘要

trastuzumab deruxtecan (T-DXd)是中国批准用于her2阳性或her2低转移性乳腺癌(MBC)患者的抗体-药物偶联物(ADC)。在中国几乎找不到真实的证据。本研究旨在探讨T-DXd在中国MBC患者中的实际有效性和安全性。方法本研究回顾性纳入了2019年12月至2024年3月在中国9家机构接受T-DXd治疗的309例MBC患者。T-DXd在21天周期的第1天以5.4 mg/kg的剂量静脉注射。使用Kaplan-Meier方法估计真实世界无进展生存期(rwPFS)和总生存期(OS)。实际不良事件(ae)按照CTCAE 4.0分级。该研究已在ClinicalTrials.gov注册(NCT05594082)。结果本组共纳入309例MBC患者,其中HER2阳性168例,HER2阴性141例(HER2-low 133例,HER2 0 8例),HER2阳性和HER2阴性患者中位年龄分别为53.5岁和55.0岁,ECOG评分中,内脏转移者为283.9%和84.4%,脑转移者为32.7%和23.4%,ECOG评分分别为14.3%和17.7%。两组接受T-DXd治疗的MBC患者的中位治疗线数(LOT)均为4。截止日期为2024年7月30日,her2阳性MBC患者的中位rwPFS和OS分别为12.1[95%可信区间(CI): 8.5-14.7]和22.7个月(95% CI: 16.6-28.8)。LOT 1-2组的rwPFS中位数为23.3个月,LOT 3-5组为12.2个月,LOT≥6组为8.2个月(P=0.001)。在her2阴性MBC患者中,中位rwPFS和OS分别为7.7 (95% CI: 6.6-8.8)和15.7个月(95% CI: 11.4-20.0)。HR+和HR-患者的中位rwPFS分别为7.7和8.1个月(P=0.870)。在her2阴性患者中,LOT 1-4组的rwPFS为9.5个月,而LOT≥6组的rwPFS为6.4个月(P=0.026)。在her2阳性(P=0.032)和阴性(P=0.039)的患者中,既往adc暴露的患者的T-DXd rwPFS均显著缩短。脑转移不影响T-DXd的疗效。任意级别ae发生率为69.3%,重度(3级及以上)ae发生率为13.9%;未观察到致死性不良反应。间质性肺疾病(ILD)发生23例(7.4%),其中15例(4.9%)为1级,4例(1.3%)为2级,4例(1.3%)为3级。80.7%的ILD患者,包括所有1级和1级2级,在对症治疗和仔细评估后再次接受T-DXd治疗。在迄今为止最大的中国MBC患者T-DXd数据集中,在重度预处理的her2阳性和her2阴性MBC患者中,T-DXd的rwPFS都令人鼓舞。在LOT较少且没有ADC暴露的MBC患者中观察到更长的rwPFS。同时,T-DXd在未充分研究的现实世界患者中显示出可控的毒性特征。经过有效的对症治疗和综合评估ILD的严重程度和恢复后,T-DXd的再挑战是可行的。本研究由北京市科技创新医学发展基金(KC2022-ZZ-0091-4)资助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world multicenter study of T-DXd treatment in Chinese patients with metastatic breast cancer

Background

Trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate (ADC) approved in China for HER2-positive or HER2-low metastatic breast cancer (MBC) patients. Little real-world evidence is available in China. This study aimed to investigate the real-world effectiveness and safety of T-DXd in Chinese MBC patients.

Methods

This study retrospectively enrolled 309 MBC patients treated with T-DXd across 9 institutions nationwide in China between December 2019 and March 2024. T-DXd was administered intravenously at a dose of 5.4 mg/kg on day 1 of a 21-day cycle. Real-world progression-free survival (rwPFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Real-world adverse events (AEs) were graded according to CTCAE 4.0. The study was registered at ClinicalTrials.gov (NCT05594082).

Findings

A total of 309 MBC patients were included, with 168 HER2-positive and 141 HER2-negative patients (133 of HER2-low and 8 of HER2 0). Among HER2-positive and HER2-negative patients, median age was 53.5 and 55.0 years, 14.3% and 17.7% ECOG scores of 2, 83.9% and 84.4% patients with visceral metastases, 32.7% and 23.4% patients with brain metastasis, respectively. The median number of lines of therapy (LOT) for MBC patients receiving T-DXd was 4 for both groups. At the cutoff date of 30 July 2024, in patients with HER2-positive MBC, median rwPFS and OS was 12.1 [95% confidence interval (CI): 8.5-14.7] and 22.7 months (95% CI: 16.6-28.8). The longer rwPFS, median 23.3 months, was observed in LOT 1-2, than 12.2 months in LOT 3-5 and 8.2 months in LOT≥6 (P=0.001). In patients with HER2-negative MBC, median rwPFS and OS was 7.7 (95% CI: 6.6-8.8) and 15.7 months (95% CI: 11.4-20.0). The median rwPFS for HR+ and HR- patients was 7.7 and 8.1 months, respectively (P=0.870). Longer rwPFS of 9.5 months was observed in LOT 1-4 compared to 6.4 months in LOT≥6 among HER2-negative patients (P=0.026). Patients with prior ADCs exposure showed significantly shorter rwPFS of T-DXd in both HER2-positive (P=0.032) and negative patients (P=0.039). Brain metastasis did not impact the effectiveness of T-DXd. Incidence of AEs of any grade was 69.3% and severe (grade 3 or above) AEs was 13.9%; no fatal AEs were observed. Interstitial lung disease (ILD) occurred in 23 patients (7.4%), with 15 (4.9%) of grade 1, 4 (1.3%) of grade 2, and 4 (1.3%) of grade 3. 80.7% of ILD patients, including all with grade 1 and one with grade 2, underwent a rechallenge with T-DXd after symptomatic treatments and careful evaluations.

Interpretation

In this largest dataset of T-DXd for Chinese patients with MBC to date, encouraging rwPFS of T-DXd was seen in heavily pretreated HER2-positive and HER2-negative MBC patients. Longer rwPFS was observed in MBC patients with fewer LOT and no prior ADC exposure. Meanwhile, T-DXd showed a manageable toxicity profile in understudied real-world patients. Rechallenge of T-DXd is feasible following effective symptomatic treatments and comprehensive assessments of ILD severity and recovery.

Funding

This work was supported by grants from Beijing Science and Technology Innovation Medical Development Foundation (KC2022-ZZ-0091-4).
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来源期刊
The Lancet Regional Health: Western Pacific
The Lancet Regional Health: Western Pacific Medicine-Pediatrics, Perinatology and Child Health
CiteScore
8.80
自引率
2.80%
发文量
305
审稿时长
11 weeks
期刊介绍: The Lancet Regional Health – Western Pacific, a gold open access journal, is an integral part of The Lancet's global initiative advocating for healthcare quality and access worldwide. It aims to advance clinical practice and health policy in the Western Pacific region, contributing to enhanced health outcomes. The journal publishes high-quality original research shedding light on clinical practice and health policy in the region. It also includes reviews, commentaries, and opinion pieces covering diverse regional health topics, such as infectious diseases, non-communicable diseases, child and adolescent health, maternal and reproductive health, aging health, mental health, the health workforce and systems, and health policy.
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