Phase 2
N=35
Cabozantinib for Metastatic Triple Negative BrCa
Breast Cancer
Bottom Line
View on ClinicalTrials.gov: NCT01738438 ↗Enrolled (actual)
35
Serious AEs
40.0%
Results posted
Jul 2016
Primary outcome: Primary: Objective Response Rate — 0.09 proportion of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Cabozantinib (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Dana-Farber Cancer Institute
- Primary completion
- May 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Objective Response Rate |
0.09 | — |
| SECONDARY Progression Free Survival |
2 | — |
Summary
In this research study, we are looking at the anti-tumor effects of Cabozantinib (XL184) in metastatic breast cancer. Data suggest that MET expression and activation are important for initiation and progression of triple-negative breast cancer (TNBC). We evaluated the efficacy of cabozantinib (XL184), a novel inhibitor of multiple receptor tyrosine kinases, including MET and VEGFR2, in patients with metastatic TNBC.
Eligibility Criteria
Inclusion Criteria
- Histologically or cytologically confirmed invasive breast cancer with stage IV disease
- Primary tumor and/or metastasis must be ER-negative, PR-negative and HER2-negative
- May have received 0-3 prior chemotherapeutic regimens for metastatic breast cancer. Must be off treatment for at least 21 days prior to enrollment
- Must have discontinued all biologic therapy at least 14 days before enrollment
- May have received prior radiation therapy in the early stage or metastatic setting, but must have completed treatment at least 14 days prior to enrollment
- Must agree to use medically acceptable methods of contraception
- Confirmed availability of formalin-fixed, paraffin-embedded tumor tissue
- Able to swallow tablets
Exclusion Criteria
- Pregnant or breastfeeding
- Received another investigational agent within 14 days prior to enrollment
- Received prior c-Met inhibitor
- Known brain metastases that are untreated, symptomatic or require therapy to control symptoms
- Psychiatric illness or social situation that could limit ability to comply with study requirements
- Require concomitant treatment in therapeutic doses with anticoagulants or antiplatelet agents
- Diagnosis of another malignancy requiring systemic treatment within the last two years (except non-melanoma skin cancer or in-situ carcinoma of the cervix)
- Known to be positive for HIV
- Active infection requiring IV antibiotics at Day 1 of cycle 1
- Uncontrolled, significant intercurrent illness
- Requires chronic concomitant treatment of a strong CYP3A4 inducer
- tumor in contact with, invading or encasing major blood vessels
- Have experienced clinically significant gastrointestinal bleeding within 6 months, hemoptysis of more than 0.5 teaspoon of red blood within 3 months or other signs indicative of pulmonary hemorrhage within 3 months of enrollment
Data sourced from ClinicalTrials.gov (NCT01738438). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.