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| ID | Type | Description | Link |
|---|---|---|---|
| HNCH-MBC12-BM04 | Other Identifier | Henan Cancer Hospital |
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This study aimed to evaluate the use of SHR-A1811 in HER2-expression Advanced Breast Cancer patients with brain metastases.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm 1 | Experimental | HER2-positive: SHR-A1811 |
|
| Arm 2 | Experimental | HER2-positive: SHR-A1811 and pyrotinib |
|
| Arm 3 | Experimental | HER2-positive: SHR-A1811 and bevacizumab |
|
| Arm 4 | Experimental | HER2-low: SHR-A1811 |
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| Arm 5 | Experimental | HER2-low: SHR-A1811 and bevacizumab |
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| Arm 6 | Experimental | HER2-low: SHR-A1811 and Adebelizumab |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SHR-A1811 | Drug | SHR-A1811: intravenous |
|
| Measure | Description | Time Frame |
|---|---|---|
| CNS-ORR by investigator | CNS-ORR was defined as percentage of participants with CNS response assessed by the investigator according to RANO-BM criteria | 2 months |
| Measure | Description | Time Frame |
|---|---|---|
| ORR by investigator using RECIST Guideline (Version 1.1) | 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 months |
| PFS |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Min Yan, Professor | Contact | +86 15713857388 | ym200678@126.com | |
| HuiMin Lv | Contact | +86 15937162120 | lvhuimin999@163.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Henan Cancer Hospital | Recruiting | Zhengzhou | Henan | China |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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| ID | Term |
|---|---|
| C000622954 | pyrotinib |
| D000068258 | Bevacizumab |
| ID | Term |
|---|---|
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
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| Pyrotinib | Drug | Pyrotinib: oral |
|
| Bevacizumab | Drug | Bevacizumab: intravenous |
|
| Adebelizumab | Drug | Adebelizumab: intravenous |
|
PFS was defined as the time from first dose to first documented disease progression (PD) or death from any cause, whichever occurred first
| up to 1.5 years |
| Adverse events | Proportion of participants experienced adverse events during the study period | up to 1.5 years |
| D017437 |
| Skin and Connective Tissue Diseases |
| D007162 |
| Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |