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NCT Number: NCT05769010

Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases

This study aimed to evaluate the use of SHR-A1811 in HER2-expression Advanced Breast Cancer patients with brain metastases.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Females and males ≥18 yrs old;
  • Pathologically confirmed HER2-positive or HER2-low advanced breast cancer;
  • At least one measurable intracranial lesion according to RANO-BM criteria, which had not received local treatment;
  • Without prior cranial radiation and had no indication for immediate local treatment or refuse to local treatment;
  • More than 2 weeks from last systemic treatment; patients with new brain lesions after craniocerebral surgery were admitted if no radiotherapy was performed. Patients with HER2-Low disease must not have systemic treatment for brain metastases.
  • Prior HER2-target treatment, endocrine therapy and chemotherapy was allowed;
  • Life expectancy is not less than 6 months.
  • Adequate function of major organs.

Exclusion criteria

  • Leptomeningeal involvement;
  • CNS complications requiring emergency neurosurgical intervention (e.g. excision, shunt tube placement);or uncontrolled symptomatic brain metastases;
  • Previous treatment with trastuzumab deruxtecan (DS-8201a) or any other antibody drug conjugate (ADC) which consists of an exatecan derivative that is a topoisomerase 1 inhibitor;
  • Patients who had progressed on previous HER2 tyrosine kinase inhibitor therapy were excluded from Arm 2, and those who had progressed on previous bevacizumab therapy were excluded from Arm 3 and Arm 5 ,and Arm 6 excludes patients who have progressed on prior PD-1 or PD-L1 therapy;
  • No concurrent antitumor therapy for metastatic cancer other than the study treatment;
  • Antitumor radiotherapy, chemotherapy, surgery, targeted therapy, or immunotherapy within 2 weeks or endocrine therapy within 1 week prior to enrolment;
  • Participated in other drug clinical trials within 4 weeks before admission;
  • History of clinically significant lung disease;
  • Other malignant tumors, excluding cured cervical carcinoma in situ, skin basal cell carcinoma or skin squamous cell carcinoma, have been diagnosed in the past five years.
  • According to the judgement of the researchers, there are concomitant diseases that seriously endanger the safety of patients or affect the completion of research (including, but not limited to, severe hypertension, severe diabetes, active infections, etc.).
  • Any other conditions that researchers believe that patients are unsuitable for this study.

Treatment and study plan

SHR-A1811

Drug

SHR-A1811: intravenous

Pyrotinib

Drug

Pyrotinib: oral

Bevacizumab

Drug

Bevacizumab: intravenous

Adebelizumab

Drug

Adebelizumab: intravenous

Primary outcomes

  1. CNS-ORR by investigator

    Time frame: 2 months

    CNS-ORR was defined as percentage of participants with CNS response assessed by the investigator according to RANO-BM criteria

Secondary outcomes

  1. ORR by investigator using RECIST Guideline (Version 1.1)

    Time frame: 2 months

    ORR was defined as percentage of participants with best (confirmed) overall response (BOR) of either CR or PR assessed by the investigator according to RECIST version 1.1

  2. PFS

    Time frame: up to 1.5 years

    PFS was defined as the time from first dose to first documented disease progression (PD) or death from any cause, whichever occurred first

  3. Adverse events

    Time frame: up to 1.5 years

    Proportion of participants experienced adverse events during the study period

Study contacts

Contact information is provided by the study sponsor or research team.

HuiMin Lv

CONTACT

[email protected]

+86 15937162120

Min Yan, Professor

CONTACT

[email protected]

+86 15713857388

Sponsors and collaborators

Lead sponsor

Henan Cancer Hospital

Other Gov

Registry information

Official study title

A Prospective, Open-label Explorative Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases

Important dates

Study start
2023
Primary completion
2028
Study completion
2029
First posted
Mar 15, 2023
Registry last updated
Apr 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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