Pyrotinib Combined With Capecitabine and Bevacizumab for Patients With HER2 Positive Breast Cancer and Brain Metastases
- Sponsor
- Tongji Hospital
- Study ID
- NCT06152822
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Breast Cancer With Brain Metastases
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- pyrotinib+capecitabine+bevacizumab — DRUGpyrotinib: ≥160mg qd capecitabine: 1000mg/m2,bid,q1-14,q3w bevacizumab:7.5mg/kg,iv,q3w
Study Details
This study intends to conduct a small, prospective, single-center clinical study to explore and evaluate the efficacy and safety of pyrrotinib combined with capecitabine and bevacizumab in HER2-positive advanced breast cancer with brain metastases.The overall objective is to provide a new drug regimen for HER2 positive breast cancer patients with brain metastases by balancing survival benefits and patient quality of life.
Key Dates
- First listed
- Dec 1, 2023
- Start date
- Nov 30, 2023
- Status verified
- Nov 2023
- Primary completion
- Nov 30, 2024
- Completion
- Nov 30, 2025
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: treatment grouppyrotinib+capecitabine+bevacizumab
Primary Outcome Measure
Objective response rate in the CNS [ Time Frame: Up to 2 years ]
Central Contacts
- Chao tengfei02783663409