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This clinical trial aim to evaluate the efficacy and safety of Pyrotinib in combination with nab-paclitaxel in patients with HER2-positive advanced breast cancer.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| pyrotinib maleate tablets+nab-paclitaxel | Experimental | pyrotinib maleate tablets: 400mg orally once daily continunously; nab-paclitaxel: 125mg/m2 iv d1、8 of each 21 day cycle, 6cycles. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| pyrotinib maleate tablets+nab-paclitaxel | Combination Product | pyrotinib maleate tablets: 400mg orally once daily continunously nab-paclitaxel: 125mg/m2 iv d1、8 of each 21 day cycle, 6cycles. |
| Measure | Description | Time Frame |
|---|---|---|
| Progress-free survival(PFS) | Baseline to measured date of progress or death from any cause | three years |
| Measure | Description | Time Frame |
|---|---|---|
| Objective response rate (ORR) | Baseline to measured stable disease | three years |
| Clinical Benefit Rate (CBR) | The percentage of subjects with Complete Response, Partial Response, or Stable Disease at least 24 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| three years |
| Disease control rate(DCR) | Rate of the patients with disease control | three years |
| Overall survival (OS) | Baseline to measured date of death from any cause | up to death |
| Safety (number of Participants with adverse events) | Adverse events Toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. The number of Participants with adverse events will be recorded at each treatment visit. | three years |