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Trastuzumab Deruxtecan Plus ivonescImab for Hormone Receptor-positive HER2 Negative Advanced Breast Cancer Study

2026年6月9日 更新者:Hongxia Wang、Fudan University

A Prospective, Single-arm, Single-center Phase II Clinical Study of Deruxtecan in Combination With ivonescImab in Hormone Receptor-positive HER2 Negative Advanced Breast Cancer

The UNITY study is a prospective, single-arm, single-center, Phase II clinical trial conducted by Fudan University Shanghai Cancer Center. It aims to evaluate the efficacy and safety of Trastuzumab Deruxtecan (T-DXd) combined with ivonescimab in patients with hormone receptor-positive (HR+), HER2-negative recurrent or metastatic breast cancer.

Approximately 53 patients will be enrolled. Eligible participants must have histologically confirmed advanced HR-positive breast cancer with HER2-low or HER2-ultralow expression. They must have experienced recurrence, metastasis, or disease progression after prior treatment with a CDK4/6 inhibitor (including in the adjuvant setting) and have received at most one line of systemic chemotherapy for advanced disease. The study permits the enrollment of patients with central nervous system (CNS) metastases.

The primary endpoint is the Overall Response Rate (ORR). Key secondary endpoints include Clinical Benefit Rate (CBR), Overall Survival (OS), Progression-Free Survival (PFS), safety, and patient-reported quality of life (assessed using EORTC QLQ-C30 and QLQ-BR23). Exploratory endpoints will involve the analysis of biomarkers from tumor and blood samples, as well as PAM50 molecular subtyping and its correlation with survival outcomes.

This study seeks to explore the efficacy and safety of Trastuzumab Deruxtecan in combination with ivonescimab for patients with HR-positive, HER2-negative recurrent or metastatic breast cancer, with a particular focus on the subpopulation with CNS metastases.

研究概览

地位

招聘中

条件

研究类型

介入性

注册 (估计的)

53

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:Hongxia Wang
  • 电话号码:86-138196379
  • 邮箱:whx365@126.com

研究联系人备份

  • 姓名:Ting Li
  • 电话号码:86-18121299346

学习地点

    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国、200032
        • 招聘中
        • Fudan University Shanghai Cancer Center
        • 接触:
          • Hongxia Wang, PHD
          • 电话号码:13524491606
          • 邮箱:whx365@126.com

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:

  1. Age ≥ 18 years, any gender.
  2. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  3. Histologically or cytologically confirmed Hormone Receptor-positive (HR+) and Human Epidermal Growth Factor Receptor 2 (HER2)-low or HER2-ultralow breast cancer, with evidence of locally recurrent or metastatic disease that is not amenable to curative-intent surgery or radiation therapy.

    • HR positivity is defined as Estrogen Receptor (ER) positive (≥1% positive cells) and/or Progesterone Receptor (PR) positive (≥1% positive cells).
    • HER2-low or HER2-ultralow expression is defined as HER2 (0 with staining), HER2 (1+), or HER2 (2+) by immunohistochemistry (IHC) with a negative in-situ hybridization (ISH) result.
    • Fulfillment of these criteria from any single pathological assessment is sufficient for eligibility.
  4. Life expectancy of ≥ 3 months.
  5. At least one measurable lesion according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1).
  6. History of recurrence or disease progression after prior treatment with a CDK4/6 inhibitor (including in the adjuvant setting). Patients have received a maximum of one line of chemotherapy for recurrent or metastatic disease. Recurrence or disease progression during or within 6 months after completion of neoadjuvant/adjuvant intravenous chemotherapy is counted as one line of therapy.
  7. Patients with Central Nervous System (CNS) metastases are eligible. Ventriculoperitoneal shunt to relieve intracranial pressure or use of mannitol, corticosteroids, or anticonvulsants is permitted prior to the first dose. However, the dose of such medications must be stable for at least 1 week without an increase, and neurological symptoms must be stable without worsening for at least 1 week. (Priority will be given to the enrollment of patients with CNS metastases.)
  8. Availability of an adequate tumor tissue sample for retrospective analysis of PD-L1 status.
  9. Adequate organ function, defined as follows:

    • Hematology: Absolute Neutrophil Count (ANC) ≥ 1.5 × 10⁹/L; Platelets (PLT) ≥ 75 × 10⁹/L; Hemoglobin (Hb) ≥ 90 g/L (transfusion or medical support to meet this level is permitted).
    • Hepatic and Renal Function: Total Bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤ 3 × ULN (≤ 5.0 × ULN in the presence of liver metastases); Blood Urea Nitrogen (BUN) or Serum Creatinine (Cr) ≤ 1.5 × ULN, or Creatinine Clearance ≥ 50 mL/min (calculated by Cockcroft-Gault formula).
    • Coagulation: Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN; Prothrombin Time (PT) ≤ 1.5 × ULN.
    • Cardiac: QT interval corrected by Fridericia's formula (QTcF) < 470 ms for females and < 450 ms for males on a 12-lead electrocardiogram (ECG); Left Ventricular Ejection Fraction (LVEF) ≥ 50% by echocardiogram.
  10. Voluntary participation in the study with signed informed consent, and willingness to comply with study procedures and follow-up.

Exclusion Criteria:

  1. Confirmed leptomeningeal metastases by Magnetic Resonance Imaging (MRI) or lumbar puncture.
  2. Prior treatment with anti-PD-1/PD-L1 or anti-VEGF agents, unless both of the following conditions are met: (1) The patient did not experience disease progression during treatment with the anti-PD-1/PD-L1 or anti-VEGF agent; and (2) The time from the last dose of the anti-PD-1/PD-L1 or anti-VEGF agent to the time of recurrence or disease progression is ≥ 3 months.
  3. Presence of third-space fluid accumulation (e.g., massive pleural or peritoneal effusion) that cannot be controlled by drainage or other methods.
  4. Receipt of whole-brain radiotherapy, chemotherapy, targeted biologic therapy, immunotherapy, surgery, or endocrine therapy within 2 weeks prior to the first dose of study drug. Bone-modifying agents for the treatment of bone metastases or prevention of osteoporosis are permitted.
  5. Prior treatment with trastuzumab deruxtecan or any antibody-drug conjugate (ADC) containing a topoisomerase inhibitor.
  6. Participation in another interventional drug clinical trial within 2 weeks prior to enrollment. Participation in non-interventional studies is allowed.
  7. Major surgery or significant trauma within 4 weeks prior to randomization, or anticipation of the need for major surgery during the study.
  8. Concurrent receipt of any other anti-cancer therapy.
  9. History of other malignancies within the past 5 years, except for curatively treated cervical carcinoma in situ, cutaneous basal cell carcinoma, cutaneous squamous cell carcinoma, and papillary thyroid carcinoma.
  10. History of any of the following cardiac conditions: (1) Myocardial infarction; (2) Congestive heart failure; (3) Any other cardiac condition judged by the investigator to be unsuitable for study participation.
  11. Known history of hypersensitivity to any component of the study drugs.
  12. History of immunodeficiency, including positive test for Human Immunodeficiency Virus (HIV), other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
  13. Active hepatitis (Hepatitis B defined as HBsAg positive and HBV DNA ≥ 1000 IU/mL; Hepatitis C defined as HCV antibody positive and HCV RNA > upper limit of normal).
  14. History of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required steroids, current ILD/pneumonitis, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening.
  15. Clinically significant pulmonary-specific comorbidities, including but not limited to any underlying pulmonary disease (e.g., pulmonary embolism within 3 months prior to the study, severe asthma, severe COPD, restrictive lung disease, pleural effusion, etc.).
  16. Uncontrolled infection requiring systemic antibiotic, antiviral, or antifungal therapy.
  17. Clear history of neurological or psychiatric disorders, including epilepsy or dementia.
  18. Pregnant or breastfeeding women; women of childbearing potential with a positive pregnancy test at baseline or who are unwilling to use effective contraceptive measures throughout the study period.
  19. Presence of any concomitant disease that, in the investigator's judgment, could seriously compromise patient safety or interfere with completion of the study (including, but not limited to, uncontrolled severe hypertension, uncontrolled severe diabetes, active infection, etc.).
  20. Any other condition for which the investigator considers 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: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
实验性的:手臂1
  • Trastuzumab Deruxtecan (T-DXd): Administered at a dose of 5.4 mg/kg via intravenous (IV) infusion on Day 1 of each 21-day cycle.
  • Ivonescimab: Administered at a dose of 20 mg/kg via intravenous (IV) infusion on Day 1 of each 21-day cycle.

Treatment for both agents will continue until disease progression or unacceptable toxicity.

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
ORR
大体时间:From treatment initiation until disease progression or death, assessed by RECIST v1.1., assessed up to 24 months
ORR is the percentage of evaluable patients with a confirmed investigator-assessed response of CR (complete response) or PR (partial response) per RECIST v1.1 .Time from randomization to disease progression or death, assessed by RECIST v1.1.
From treatment initiation until disease progression or death, assessed by RECIST v1.1., assessed up to 24 months

次要结果测量

结果测量
措施说明
大体时间
PFS
大体时间:From treatment initiation until disease progression or death, assessed by RECIST v1.1., whichever occurs first, assessed up to 24 months.
PFS is the time from the date of first dose until the date of objective radiographic disease progression or death (by any cause in the absence of progression).
From treatment initiation until disease progression or death, assessed by RECIST v1.1., whichever occurs first, assessed up to 24 months.
OS
大体时间:From treatment initiation until death from any cause, assessed up to 36 months.
OS is the time from the date of frst dose until the date of death by any cause.
From treatment initiation until death from any cause, assessed up to 36 months.
Clinical Benefit Rate
大体时间:From treatment initiation until disease progression or death, assessed by RECIST v1.1., whichever occurs first, assessed up to 24 months.
CBR is defined as the percentage of patients who achieve a Complete Response (CR), a Partial Response (PR), or have Stable Disease (SD) lasting for at least 24 weeks.
From treatment initiation until disease progression or death, assessed by RECIST v1.1., whichever occurs first, assessed up to 24 months.
Safety assessed by NCI-CTCAE v5.0
大体时间:From the first dose of study treatment until 30 days after the last dose of study treatment, assessed up to approximately 2 years.
Safety and tolerability will be evaluated by monitoring and recording all adverse events (AEs). The severity of AEs will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0. AEs are defined as any adverse event that starts or worsens in severity on or after the first dose of study treatment.
From the first dose of study treatment until 30 days after the last dose of study treatment, assessed up to approximately 2 years.
Quality of Life Assessed by EORTC QLQ-C30
大体时间:Screening, within 3 days before each treatment administration, at the end of treatment, and during safety follow-up, assessed up to 24 months.
The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) is a validated cancer-specific quality-of-life instrument. Scores are transformed to a 0-100 scale according to the EORTC scoring manual. Higher functional scores indicate better functioning, whereas higher symptom scores indicate greater symptom burden. Change from baseline will be evaluated.
Screening, within 3 days before each treatment administration, at the end of treatment, and during safety follow-up, assessed up to 24 months.
Breast cancer-specific quality of life assessed by EORTC QLQ-BR45
大体时间:Screening, within 3 days before each treatment administration, at the end of treatment, and during safety follow-up, assessed up to 24 months.
The EORTC QLQ-BR45 is a validated breast cancer-specific quality-of-life questionnaire consisting of functional and symptom scales. Scores are transformed to a 0-100 scale according to the EORTC scoring manual. Higher functional scores indicate better functioning, whereas higher symptom scores indicate greater symptom burden.
Screening, within 3 days before each treatment administration, at the end of treatment, and during safety follow-up, assessed up to 24 months.

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 (实际的)

2026年4月1日

初级完成 (估计的)

2027年12月30日

研究完成 (估计的)

2028年2月1日

研究注册日期

首次提交

2025年12月13日

首先提交符合 QC 标准的

2026年6月9日

首次发布 (实际的)

2026年6月15日

研究记录更新

最后更新发布 (实际的)

2026年6月15日

上次提交的符合 QC 标准的更新

2026年6月9日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

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

在美国制造并从美国出口的产品

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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