Clinical Trial Details
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[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT03412955 : A Pilot Study of Eribulin in Breast Cancer (BC) Patients With Brain Metastases Previously Treated With Anthracyclines and Taxanes
PhasePhase 2
AgesMin: 21 Years Max: 99 Years
Eligibility
Inclusion Criteria:

1. Female patients with histologically or cytologically confirmed carcinoma of the
breast.

2. Patients with locally advanced or metastatic disease who have received an
anthracycline (e.g. doxorubicin, epirubicin) and a taxane (e.g. paclitaxel,
docetaxel), either in combination or in separate regimens. It can be used in
neo-adjuvant, adjuvant or metastatic setting.

3. Patients must have measurable brain metastases (minimum size of 10mm in long axis)
which is asymptomatic and does not required any treatment or had failed to respond or
progress after either radiation treatment or stereotactic radiosurgery.

4. Patients who are deemed to have asymptomatic brain metastases should not be on
systemic corticosteroid at enrolment. Patients who have brain metastases that have
failed previous radiation therapy or stereotactic radiosurgery are allowed to be on
systemic corticosteroid at enrolment. Baseline dose of corticosteroid should be
documented.

5. Patients with known HER2 positive tumors may additionally have been treated with
trastuzumab and/or pertuzumab or trastuzumab emtasine in centers where this treatment
is available.

6. Patients with known estrogen and/or progesterone receptor-expressing tumors may have
additionally been treated with hormonal therapy

7. Resolution of all previous chemotherapy or radiation-related toxicities to Grade 1
severity or lower, except for stable sensory neuropathy =Grade 2 and alopecia

8. Age above 21 years

9. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1 or 2

10. Life expectancy of more than 3 months

11. Adequate renal function as evidenced by serum creatinine < 1.5 mg/dL or calculated
creatinine clearance > 50 mL/minute (min) per the Cockcroft and Gault formula

12. Adequate bone marrow function as evidenced by absolute neutrophil count (ANC) above
1.5 x 109/L, hemoglobin above 10.0 g/dL, and platelet count above 100 x 109/L.

13. Adequate liver function as evidenced by bilirubin less than 1.5 times the upper limits
of normal (ULN) and alkaline phosphatase, alanine transaminase (ALT), and aspartate
transaminase (AST) less than 3 x ULN (in the case of liver metastases less than 5 x
ULN), or in case of bone metastases, liver specific alkaline phosphatase less than 3 x
ULN

14. Patient's willing and able to comply with the study protocol for the duration of the
study

15. Written informed consent prior to any study-specific screening procedures with the
understanding that the patient may withdraw consent at any time without prejudice.
However, hormonal therapy must be discontinued one week before administration of study

Exclusion Criteria:

1. Patients who have received chemotherapy, radiation, or biological therapy within two
weeks, or hormonal therapy within one week before study treatment start, or any
investigational drug within four weeks before study treatment start.

2. Women who are pregnant or breast-feeding; women of childbearing potential with either
a positive pregnancy test at screening or no pregnancy test; women of childbearing
potential unless (1) surgically sterile or (2) using adequate measures of
contraception (considered to be two methods of contraception, one of which must be a
barrier method, e.g. condom, diaphragm or cervical cap). Perimenopausal women must be
amenorrheic for at least 12 months to be considered of non-childbearing potential.

3. Severe/uncontrolled intercurrent illness/infection.

4. Significant cardiovascular impairment (history of congestive heart failure > NYHA
grade II, unstable angina or myocardial infarction within the past six months, or
serious cardiac arrhythmia)

5. Patients with known positive HIV status

6. Patients who have had a prior malignancy, other than carcinoma in situ of the cervix,
or non-melanoma skin cancer, unless the prior malignancy was diagnosed and
definitively treated above 5 years previously with no subsequent evidence of
recurrence

7. Patients with neuropathy > Grade 2 at screening.

8. Patients with QTC > 500 msec at screening.

9. Concurrent hormonal therapy for metastatic breast cancer is not allowed. However, Her2
positive metastatic breast cancer patients who progressed on prior anti-Her2 directed
therapy may have concurrent eribulin and trastuzumab, but not trastuzumab emtasine.

10. Patient with leptomeningeal only disease, without other measurable brain metastasis,
is excluded.
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT03412955      |      Link to official Clinicaltrials.gov listing
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