SHR-A1811 Monotherapy or Sequential THPy as Neoadjuvant Therapy for Stage II-III HER2-Positive Breast Cancer
2026年8月24日 更新者:First Affiliated Hospital of Zhejiang University
A Prospective, Multicenter, Exploratory Clinical Study Evaluating the Efficacy and Safety of SHR-A1811 Monotherapy or Sequential THPy as Neoadjuvant Therapy in Stage II-III HER2-positive Breast Cancer
This is a prospective, open-label, phase II, multicenter exploratory clinical study.
Eligible female patients aged 18-75 years with stage II-III HER2-positive breast cancer will receive 4 cycles of SHR-A1811 (4.8 mg/kg, intravenous infusion every 3 weeks).
After 4 cycles, tumor response will be assessed per RECIST 1.1 criteria.
Patients with a ≥50% reduction in tumor burden will continue with another 4 cycles of SHR-A1811 followed by definitive surgery.
Patients with <50% reduction will receive 4 cycles of the THPy regimen (docetaxel + trastuzumab + pyrotinib) before surgery.
Circulating tumor DNA (ctDNA) will be assessed for minimal residual disease (MRD) at baseline, after 4 cycles of treatment, and postoperatively.
The primary endpoint is total pathological complete response (tpCR), assessed by an independent review committee (IRC).
This study aims to evaluate the efficacy, safety, and feasibility of imaging- and MRD-guided neoadjuvant therapy in HER2-positive breast cancer.
研究概览
研究类型
介入性
注册 (估计的)
80
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
- 姓名:Peifen Fu
- 电话号码:0571-87236852
- 邮箱:Fupeifen@hotmail.com
学习地点
-
-
Zhejiang
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Hangzhou、Zhejiang、中国、310003
- The First Affiliated Hospital, Zhejiang University School of Medicine
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首席研究员:
- Peifen Fu
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接触:
- Minya Yao
- 电话号码:13634111760
- 邮箱:yminya@163.com
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首席研究员:
- Minya Yao
-
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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 aged ≥18 years and ≤75 years.
- Histopathologically confirmed invasive breast cancer with no prior systemic anti-tumor therapy for breast cancer.
- Histopathologically confirmed HER2-positive status in accordance with the 2018 ASCO-CAP HER2 testing guideline criteria: immunohistochemistry (IHC) score of 3+, or IHC 2+ with positive in situ hybridization (ISH) test (ISH amplification ratio ≥2.0); hormone receptor status must be available.
- Stage II-III breast cancer per the 8th edition AJCC Breast Cancer Staging System.
- At least one measurable target lesion according to RECIST Version 1.1.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Adequate function of major organs as defined below (no blood transfusion, granulocyte-stimulating factors or thrombopoietic agents administered within 2 weeks prior to screening):
- Hematology: absolute neutrophil count (ANC) >1.5×10⁹/L; platelet count (PLT) >75×10⁹/L; hemoglobin (Hb) >90 g/L.
- Serum biochemistry: total bilirubin (TBIL) <1.5×upper limit of normal (ULN); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <1.5×ULN; alkaline phosphatase <2.5×ULN; blood urea nitrogen (BUN)/urea and creatinine (Cr) <1.5×ULN.
- Echocardiogram: left ventricular ejection fraction (LVEF) ≥55%.
- 12-lead electrocardiogram: Fridericia-corrected QT interval (QTcF) <470 msec.
- For premenopausal women of childbearing potential: serum or urine pregnancy test must be negative within 7 days before treatment initiation; not breastfeeding. All participants must use effective barrier contraception throughout treatment and for 6 months after completion of study treatment.
- Voluntarily provide written informed consent, demonstrate good compliance and willingness to complete scheduled visits and study-related procedures.
Exclusion Criteria:
- Stage IV breast cancer.
- Inflammatory breast cancer.
- Prior anti-tumor therapy or radiotherapy for any malignancy, or concurrent other malignant tumors, except cured carcinoma in situ of cervix, basal cell carcinoma or squamous cell carcinoma.
- Concurrent receipt of anti-tumor therapy in another clinical trial, including but not limited to chemotherapy, endocrine therapy, biotherapy, bone-modifying agent therapy or immune checkpoint inhibitor therapy.
- Major surgery unrelated to breast cancer performed within 4 weeks prior to the first dose of study drug, or participants who have not fully recovered from such surgery.
Severe cardiac disorders, including but not limited to:
- Confirmed history of heart failure or systolic dysfunction (LVEF <50%).
- High-risk uncontrolled arrhythmias, such as atrial tachycardia with resting heart rate >100 bpm, significant ventricular arrhythmia (e.g., ventricular tachycardia), or advanced atrioventricular block (Mobitz type II second-degree or third-degree atrioventricular block).
- Angina requiring anti-anginal medication.
- Electrocardiogram evidence of transmural myocardial infarction.
- Poorly controlled hypertension (systolic blood pressure >180 mmHg and/or diastolic blood pressure >100 mmHg) despite medical treatment.
- Uncontrolled active infection requiring treatment; history of immunodeficiency including positive HIV test, other acquired or congenital immunodeficiency disorders, or history of organ transplantation.
- Known hypersensitivity to any components of study drugs specified in this protocol.
- Pregnant or breastfeeding women; women of childbearing potential with positive baseline pregnancy test; women of childbearing potential unwilling to use effective contraception throughout the study and for 6 months after the last study drug administration.
- Known or suspected interstitial lung disease; moderate to severe pulmonary diseases that may interfere with detection or management of drug-related pulmonary toxicity and severely impair respiratory function within 3 months before 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; any autoimmune, connective tissue or inflammatory diseases involving the lung such as rheumatoid arthritis, Sjogren's syndrome, sarcoidosis; or prior history of pneumonectomy.
- Severe concomitant illnesses or other comorbidities that would interfere with planned treatment, or any other conditions rendering the participant unsuitable for participation in the study as judged by the investigator.
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:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:SHR-A1811 with Response-Guided Therapy
All participants receive an initial 4 cycles of SHR-A1811 (4.8 mg/kg, intravenous infusion every 3 weeks).
After 4 cycles, tumor response is assessed per RECIST 1.1 criteria.
Participants with ≥50% tumor regression continue with another 4 cycles of SHR-A1811, followed by definitive surgery.
Participants with <50% regression switch to 4 cycles of the THPy regimen (docetaxel + trastuzumab + pyrotinib) before surgery.
This is a single-arm, non-randomized, open-label, response-guided treatment strategy.
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SHR-A1811, 4.8 mg/kg, intravenous infusion once every 3 weeks.
All patients receive initial 4 cycles; responders continue additional 4 cycles before surgery.
Combined regimen of docetaxel, trastuzumab, and pyrotinib.
Administered for 4 cycles to patients with insufficient tumor response after the initial 4 cycles of SHR-A1811 prior to definitive surgery.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Rate of total pathological complete response (tpCR)
大体时间:At the time of definitive surgery (approximately 24 weeks after enrollment)
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At the time of definitive surgery (approximately 24 weeks after enrollment)
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Rate of breast pathological complete response (bpCR)
大体时间:At the time of definitive surgery (approximately 24 weeks after enrollment)
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At the time of definitive surgery (approximately 24 weeks after enrollment)
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Objective Response Rate (ORR)
大体时间:After 2 cycles of study treatment (approximately 6 weeks after enrollment)
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After 2 cycles of study treatment (approximately 6 weeks after enrollment)
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其他结果措施
结果测量 |
大体时间 |
|---|---|
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Incidence and severity of Adverse Events (AEs)
大体时间:From first study drug administration up to 30 days after the last dose of study treatment
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From first study drug administration up to 30 days after the last dose of study treatment
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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9月1日
初级完成 (估计的)
2029年4月1日
研究完成 (估计的)
2030年10月1日
研究注册日期
首次提交
2026年8月24日
首先提交符合 QC 标准的
2026年8月24日
首次发布 (实际的)
2026年8月26日
研究记录更新
最后更新发布 (实际的)
2026年8月26日
上次提交的符合 QC 标准的更新
2026年8月24日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他研究编号
- 26-OBU-ZJ-BC-II-020
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
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.