Clinical trial

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

Name
HNCH-MBC12
Description
This study aimed to evaluate the use of SHR-A1811 in HER2-expression Advanced Breast Cancer patients with brain metastases.
Trial arms
Trial start
2023-03-31
Estimated PCD
2025-10-30
Trial end
2026-04-30
Status
Recruiting
Phase
Early phase I
Treatment
SHR-A1811
SHR-A1811: intravenous
Arms:
Arm 1, Arm 2, Arm 3, Arm 4
Pyrotinib
Pyrotinib: oral
Arms:
Arm 2
Bevacizumab
Bevacizumab: intravenous
Arms:
Arm 3
Size
100
Primary endpoint
CNS-ORR by investigator
2 months
Eligibility criteria
Inclusion Criteria: 1. Females ≥18 yrs old; 2. Pathologically confirmed HER2-positive or HER2-low advanced breast cancer; 3. At least one measurable intracranial lesion according to RANO-BM criteria, which had not received local treatment; 4. Without prior cranial radiation and had no indication for immediate local treatment or refuse to local treatment; 5. 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. 6. Prior HER2-target treatment, endocrine therapy and chemotherapy was allowed; 7. Life expectancy is not less than 6 months. 8. Adequate function of major organs. Exclusion Criteria: 1. Leptomeningeal involvement; 2. CNS complications requiring emergency neurosurgical intervention (e.g. excision, shunt tube placement);or uncontrolled symptomatic brain metastases; 3. 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; 4. 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; 5. No concurrent antitumor therapy for metastatic cancer other than the study treatment; 6. Antitumor radiotherapy, chemotherapy, surgery, targeted therapy, or immunotherapy within 2 weeks or endocrine therapy within 1 week prior to enrolment; 7. Participated in other drug clinical trials within 4 weeks before admission; 8. History of clinically significant lung disease; 9. 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. 10. 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.). 11. Any other conditions that researchers believe that patients are unsuitable for this study.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 100, 'type': 'ESTIMATED'}}
Updated at
2023-10-19

1 organization

2 products

1 drug

1 abstract

1 indication

Indication
Breast Cancer
Product
Pyrotinib
Abstract
Efficacy and safety of HER2-ADC SHR-A1811 in HER2-positive breast cancer with brain metastases.
Org: Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital,