Peking University Cancer Hospital & Institute
Beijing, Beijing Municipality, 100142, China
NCT Number: NCT01589159
This is a single-center, open-lable, non-comparative, prospective, phase Ⅱ efficacy and safety study. Eligible patients are enrolled in a single group. The investigators propose to determine the efficacy and safety of low-dose metronomic chemotherapy with Etoposide/Capecitabine in Patients with Metastatic Breast Cancer Previously Treated with Anthracyclines and/or Taxanes.
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Notify Me18 year–80 year
Female
Interventional
Phase 2
Beijing, Beijing Municipality, 100142, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Drug:capecitabine 700mg/m2, twice daily on days 1-14.
Etoposide 30mg/m2, once daily on days 1-7.
Time frame: 24 weeks after the treatment
Clinical benefit is defined as CR, PR, SD≥24 weeks.
Tao OUYANG
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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