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| Name | Class |
|---|---|
| Eli Lilly and Company | INDUSTRY |
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The primary purpose of our study is to evaluate whether gemcitabine as a single agent is superior to observation in improving progression-free survival (PFS) in patients with metastatic breast cancer (MBC) who achieved disease control with an initial six cycles of PG as their first-line treatment
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Gemcitabine, Experimental | Gemcitabine 1250 mg/m2, IV on day 1 of 21 day cycle,with a follow up for every 12 weeks until disease progression or the date of first documented death from any cause | ||
| Observational | Observation for every 12 weeks until disease progression or the date of first documented death from any cause |
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| Measure | Description | Time Frame |
|---|---|---|
| PFS | From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 3 years | From randomization to disease progression |
| PFS(progression free survival) | time from the date of randomization until the date of disease progression,assessed up to 3 years | |
| PFS(progression free survival) | PFS was defined as the time from the date of randomization until the date of disease progression at any site including distant metastasis or second primary tumors or death,assessed up to 3 years | the time from the date of randomization until the date of disease progression,assessed up to 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| OS(overall survival) | the time from date of randomization until the date of first documented death from any cause,assessed up to 3 years | the time from date of randomization until the date of first documented death from any cause,assessed up to 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| QoL(quality of life) | the time from enrollment to disease progression or the date of first documented death,whichever comes first,to observe the quality of life in participants,assessed up to 3 years | the time from enrollment to disease progression or the date of first documented death,assessed up to 3 years |
Inclusion Criteria:
Exclusion Criteria:
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Patients with MBC exhibited disease control (complete response + partial response + stable disease) with first-line PG and were randomly assigned to maintenance chemotherapy or observation.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Li Nanlin, Ph.D | Contact | +86-137-0911-3279 | nanlin-74@163.com | |
| Chen Cong, Master | Contact | +86-136-4929-4730 | congcongfeiyang@126.com |
| Name | Affiliation | Role |
|---|---|---|
| Li Nanlin, Ph.D | Air Force Military Medical University, China | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Xijing Hospital , Fourth Military Medical University | Recruiting | Xi'an | Shaanxi | 710032 | China |
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| ID | Term |
|---|---|
| D012008 | Recurrence |
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009371 | Neoplasms by Site |
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2 ml blood sample is needed before enrollment.
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |