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Efficacy and Safety of Trastuzumab Rezetecan or Trastuzumab Deruxtecan in Advanced Breast Cancer

A Comparison of the Efficacy and Safety of Trastuzumab Rezetecan(SHR-A1811) Versus Trastuzumab Deruxtecan(DS-8201) in Patients With HER2-Positive Metastatic Breast Cancer Previously Treated With Trastuzumab

This study is a prospective, open-label, multicenter, randomized, parallel Phase II clinical trial. This study aims to investigate the efficacy and safety of trastuzumab rezetecan or trastuzumab deruxtecan in HER2 positive advanced/metastastic breast cancer

研究概览

研究类型

介入性

注册 (估计的)

100

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

  • 姓名:herui Yao, PhD, MD
  • 电话号码:+86 13500018020
  • 邮箱:yaoherui@163.com

学习地点

    • Guangdong
      • Guangzhou、Guangdong、中国
        • Sun Yat-sen Memorial Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Female patients aged ≥18 and ≤75 years.
  • Histologically or cytologically confirmed HER2-positive (IHC 3+ and/or ISH positive) unresectable or metastatic breast cancer.
  • Prior treatment with trastuzumab and a taxane in the recurrent or metastatic setting. Or recurrence during or within 12 months (disease-free interval, DFI) after completing neoadjuvant/adjuvant chemotherapy and/or anti-HER2 targeted therapy.
  • Documented radiological disease progression (during or after the most recent prior therapy).
  • ECOG Performance Status of 0 or 1.
  • At least one measurable lesion according to RECIST v1.1 criteria.
  • Adequate organ function meeting the following criteria (without the use of any blood components, cytokines, or growth factors for correction within 14 days prior to the first dose):

Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L; Platelet count (PLT) ≥100 × 10⁹/L; Hemoglobin (Hb) ≥90 g/L (9.0 g/dL); Albumin ≥3.0 g/dL;Total bilirubin ≤1.5 × ULN; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × ULN (≤5.0 × ULN for patients with liver metastases); Serum creatinine ≤1.5 × ULN OR creatinine clearance ≥60 mL/min (calculated using the Cockcroft-Gault formula); QTcF interval ≤470 ms; Left ventricular ejection fraction (LVEF) ≥50% as measured by echocardiography (ECHO) or multigated acquisition scan (MUGA)

  • Female subjects of childbearing potential must have a negative pregnancy test at screening and must agree to use highly effective contraception methods from the signing of the informed consent form until 7 months after the last dose of the investigational product.
  • Willing and able to provide written informed consent, with good compliance, and willing to cooperate with follow-up visits and study-related procedures.

Exclusion Criteria:

  • Patients with known untreated spinal cord compression or active central nervous system (CNS) metastases, except for those who have been treated and have remained stable for at least 1 month and have discontinued corticosteroids for >2 weeks.
  • History of other malignancies within the past 5 years, excluding cured basal cell carcinoma of the skin and carcinoma in situ of the cervix.
  • Uncontrolled third-space fluid accumulation (e.g., massive ascites, pleural effusion, pericardial effusion) that cannot be managed by drainage or other methods.
  • Having undergone major cancer-related surgery, radiotherapy, chemotherapy, immunotherapy, molecular targeted therapy, biotherapy, or other clinical investigational therapy within 4 weeks prior to the first dose.
  • Prior treatment with an antibody-drug conjugate containing an exatecan derivative (a topoisomerase I inhibitor).
  • Use of immunosuppressants or systemic corticosteroids for immunosuppressive purposes (at doses >10 mg/day prednisone or equivalent) within 2 weeks prior to the first dose, excluding topical, nasal spray, or inhaled corticosteroids.
  • Presence of any active autoimmune disease or a history of autoimmune disease that may potentially recur.
  • History of immunodeficiency, including a positive HIV test, other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
  • Patients with known or suspected interstitial lung disease (ILD); or presence of other moderate-to-severe pulmonary diseases that may significantly impair respiratory function or interfere with the detection or management of drug-related pulmonary toxicity within 3 months prior to the first dose, including but not limited to idiopathic pulmonary fibrosis, organizing pneumonia/bronchiolitis obliterans, pulmonary embolism, severe asthma, severe chronic obstructive pulmonary disease (COPD), obstructive/restrictive lung disease, etc.; and any autoimmune, connective tissue, or inflammatory disorders involving the lungs, such as rheumatoid arthritis, Sjögren's syndrome, sarcoidosis, etc.; or history of pneumonectomy. Patients who experienced ≥Grade 3 ILD during prior treatment with immune checkpoint inhibitors are excluded.
  • Presence of active hepatitis B (HBsAg positive and HBV DNA ≥500 IU/mL), hepatitis C (anti-HCV positive and HCV RNA above the upper limit of normal), or liver cirrhosis; or severe infections requiring systemic antibiotic, antiviral, or antifungal therapy.
  • Toxicities from prior anti-tumor therapy that have not recovered to ≤ Grade 1 (according to NCI-CTCAE v6.0).
  • Known hypersensitivity to any of the study drugs or their excipients.
  • Any other severe physical or mental illness or abnormal laboratory finding that, in the investigator's judgment, may increase the risk associated with study participation, interfere with the study results, or make the patient unsuitable for participation in this study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:SHR-A1811
SHR-A1811 4.8mg/kg iv q3w
其他名称:
  • SHR-A1811
  • T-DXH
  • Trastuzumab rezetecan
有源比较器:T-DXd
T-DXd 5.4mg/kg iv q3w
其他名称:
  • T-DXd
  • DS-8201
  • 曲妥珠单抗deruxtecan

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Progression Free Survival(PFS)
大体时间:From the date of randomization to the earliest date of the first objective documentation of radiographic disease progression or death due to any cause, up to approximately 3 years
Time from the date of randomization until the date of first documented radiological disease progression (PD) or death from any cause, whichever occurs first. If a subject did not experience PD or death by the data cutoff date, or had received other anti-tumor therapy, censoring occurred at the date of the last efficacy assessment prior to the cutoff date or the start date of other anti-tumor therapy, whichever was earlier.
From the date of randomization to the earliest date of the first objective documentation of radiographic disease progression or death due to any cause, up to approximately 3 years

次要结果测量

结果测量
措施说明
大体时间
治疗期间出现的不良事件(TEAEs)和治疗期间出现的严重不良事件(TESAEs)
大体时间:从首次服用研究药物(第1天)起至约3年
从首次服用研究药物(第1天)起至约3年
Objective response rate (ORR)
大体时间:From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
The percentage of subjects in the analysis set whose best overall response (BOR) was a complete response (CR) or partial response (PR) from the start of the study treatment until the subject discontinued the study due to disease progression. It is recommended to use the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) to evaluate the objective tumor response. Subjects must have measurable tumor lesions at baseline, and the assessment of efficacy is recommended to be categorized according to RECIST 1.1 criteria into complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD).
From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
Disease control rate(DCR)
大体时间:From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
The percentage of subjects in the analysis set whose best overall response (BOR) was complete response (CR), partial response (PR), or stable disease (SD) from the start of the study treatment regimen until the subject discontinued the study due to disease progression. It is recommended to use the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) to assess the objective tumor response. Subjects must have measurable tumor lesions at baseline, and the efficacy assessment is recommended to be categorized according to RECIST 1.1 criteria as complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD).
From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
Duration of Response(DOR)
大体时间:From the date of the first documented objective response (CR or PR) to the first documented disease progression or death, whichever occurs first, up to approximately 3 years
defined as the time from the date of first documented response (complete response, CR, or partial response, PR, whichever occurs first) to the date of disease progression or death, whichever occurs earlier. Response is assessed using the Response Evaluation Criteria in Solid Tumors (RECIST 1.1).
From the date of the first documented objective response (CR or PR) to the first documented disease progression or death, whichever occurs first, up to approximately 3 years
Overall survival (OS)
大体时间:From the date of randomization up to the date of death due to any cause, up to approximately 3 years
Defined as the time from the date of enrollment to the date of death from any cause. For subjects who were alive at the last follow-up, their OS data are censored at the date of the last follow-up. For subjects who were lost to follow-up, their OS data are censored at the date of the last documented evidence of survival prior to being lost. Censored OS is defined as the time from enrollment to censoring.
From the date of randomization up to the date of death due to any cause, up to approximately 3 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月1日

初级完成 (估计的)

2031年6月1日

研究完成 (估计的)

2031年12月1日

研究注册日期

首次提交

2026年6月1日

首先提交符合 QC 标准的

2026年6月1日

首次发布 (实际的)

2026年6月5日

研究记录更新

最后更新发布 (实际的)

2026年6月5日

上次提交的符合 QC 标准的更新

2026年6月1日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • MA-BC-II-137

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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