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Clinical Trials/EUCTR2007-006025-27-IT
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

ISTITUTO EUROPEO DI ONCOLOGIA0 sitesFebruary 20, 2008

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.

Registry
who.int
Start Date
February 20, 2008
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

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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