EUCTR2007-006025-27-IT
Active, not recruiting
Not Applicable
A phase II study of metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with bevacizumab and erlotinib (BEXE), plus trastuzumab in HER2/neu positive tumors (BEXET), in advanced breast cancer
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- advanced or metastatic breast cancer
- Sponsor
- ISTITUTO EUROPEO DI ONCOLOGIA
- Status
- Active, not recruiting
- Last Updated
- 13 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Pre\- or post\-menopausal women with histologically proven, locally advanced
- •(inoperable) or metastatic breast carcinoma.
- •Immunohistochemical receptor status at the last biopsy available:
- •ER and PgR absent (0% of the cells) or
- •ER or PgR Absent or
- •ER and PgR ≤ 50% of the cells
- •Measurable disease
- •Age \>18 years
- •Life expectancy of greater than 6 months.
- •Are the trial subjects under 18? no
Exclusion Criteria
- •Previous treatment with bevacizumab, EGFR inhibitors or metronomic cyclophosphamide \+ capecitabine.
- •Immunohistochemical receptor status at the last biopsy available:
- •ER and PgR≥50%
- •Presence of cerebral or leptomeningeal involvement.
Outcomes
Primary Outcomes
Not specified
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