Inclusion Criteria:
- - Subjects must meet all of the following criteria to be enrolled:
- Male/Female.
- - At least 18 years of age.
- - Histologically confirmed HER2 negative breast cancer determined from the most
recent tumor sample (primary or metastatic), as per the current American Society
of Clinical Oncology and College of American Pathologists HER2 testing
guidelines.
- - For ER positive breast cancer patients: prior treatment with a CDK4/6 inhibitor
and endocrine therapy in required in the metastatic settings.
If a patient has
received a CDK4/6 inhibitor plus endocrine therapy in the adjuvant settings and
the cancer recurred while on the CDK4/6 inhibitor or within 12 months of the end
of CDK4/6 inhibitor treatment, then the patient will eligible without getting a
CDK4/6 inhibitor and endocrine therapy in the metastatic setting.
- - For triple negative breast cancer patients: no specific prior anti-cancer
treatment is required.
- - Have radiological evidence of one or more brain metastases.
- - Ability to obtain an MRI.
- - Has a radiological evidence of a measurable disease (per RECIST 1.1) outside of
the brain which is accessible to a biopsy.
- - Willing to undergo a research core biopsy of the tumor tissue.
- - Considered to be medically fit for undergoing a biopsy.
- - Subjects anticipated by the investigator to be a candidate for systemic therapy
immediately or in the future.
- - Ability to understand the investigational nature of the study and sign the
informed consent.
- - Key Criteria for Step 1 Registration:
- Abnormally active HER2 signaling as determined by the CELsignia test on the tumor
tissue.
- - New or progressive brain metastases defined as any one of the following:
- Untreated measurable lesions in patients who have received surgery and/or
stereotactic radiosurgery (SRS) to one or more other lesions.
- - Residual or progressive lesions after surgery if asymptomatic.
- - Patients who have had prior whole-brain radiotherapy (WBRT) and/or SRS and then
whose lesions have progressed by RANO-BM criteria or there are new lesions are
eligible.
Lesions treated with SRS may be eligible if there is unequivocal
evidence of progression.
- - Patients who have not previously been treated with cranial radiation (e.g., WBRT
or SRS) are eligible, but such patients must be asymptomatic and neurologically
stable from their CNS metastases.
- - Measurable brain metastases with at least one lesion > 5 mm in longest diameter
AND is/are new or progressive lesion/s as defined by criterion B.
- - No major surgery within 10 days prior to registration.
Surgeries should be
avoided any time after registration during the study treatment, but minor
procedures like dental extractions and surgeries deemed important to maintain or
improve patients' quality of life and are allowed.
- - A minimum of 14 days since the last dose of chemotherapy except for the optional
pre-Step 1 capecitabine.
If pre-step 1 optional capecitabine was administered,
then a minimum of 7 days from the last dose of Capecitabine is required before
registration. There is no limit on the number of previous chemotherapy regimens
for eligibility.
- - A minimum of 7 days since the last dose of any hormonal therapy (no limit on the
number of previous hormonal regimens for eligibility) except fulvestrant.
A
minimum of 28 days since the last dose of fulvestrant before registration.
- - A minimum of 21 days since the last dose of targeted therapy (e.g., a CDK4/6
inhibitor, PI3kinase inhibitors, etc.)
- A minimum of 7 days since the last fraction of extracranial radiation and has
recovered from any acute toxic effects of radiation therapy.
- - A minimum of 30 days since the last dose of any investigational cancer treatment
or any immunotherapy.
- - ECOG performance status of 0 -2.
- - Left ventricular ejection fraction ≥ 50% at baseline.
- - Prior treatment-related major organ toxicities recovered to ≤grade 1.
- - Adequate bone marrow, hepatic, renal, and coagulation function.
- - Post-menopausal, surgically sterile, or willing to use a reliable form of
contraception while on the study and for 180 days after discontinuing either
study treatment.
The patients that can father children are willing to use highly
effective contraception for at least 90 days following last dose of either study
treatment.
- - Ability to understand the investigational nature of the study and sign the
informed consent.
Exclusion Criteria:
- - Subjects must NOT meet any of the following criteria to be enrolled:
- Patients who have received capecitabine for the treatment of the current breast
cancer in the metastatic setting.
- - Patients who have received capecitabine only in the perioperative setting for the
primary early-stage breast cancer AND the breast cancer recurred while taking
capecitabine or within 180 days of the last dose of capecitabine therapy.
- - History of other malignancies other than the following: 1.
adequately treated
non-melanoma skin cancer, 2. curatively treated in-situ cancer of the cervix 3.
other solid tumors which have been curatively treated AND no evidence of
recurrence in the last 2 years.
- - Gastrointestinal tract disease resulting in an inability to absorb oral
medication.
- - Known hypersensitivity to the study drugs or their components.
- - Pregnant or breast-feeding.
- - Known or suspected leptomeningeal disease.
- - Known bleeding or coagulation issues, subject taking anticoagulants or having
bleeding diathesis that may significantly increase the risk of bleeding during
the biopsy.
If the subject is on anticoagulation, perioperative management of
anticoagulation should be done per institutional practice.
- - Chronic and concomitant use of strong or moderate CYP3A4 inhibitors and strong or
moderate CYP3A4 inducers.
These drugs should be stopped at least 14 days prior to
registration to Step 0.
- - Current uncontrolled medical conditions that could limit a subject's ability to
undertake study therapy.
- - Inflammatory bowel disease with diarrhea as a major component.
- - Key Criteria for Step 1:
Subjects must NOT meet any of the following criteria to be enrolled:
- Normally active HER2 signaling as determined by the CELsignia test on the tumor tissue.
- - Inconclusive HER2 signaling testing by the CELsignia test on the tumor tissue.
- - Whole-brain radiotherapy in the prior three months.
- - Resting blood pressure higher than systolic of 160 and/or diastolic of 110 mmHg or
poorly controlled hypertension, history of labile hypertension, or poor compliance
with anti-hypertensive medication.
- - Serious cardiac illness or condition including, but not limited to, clinically
significant congestive heart failure, high-risk uncontrolled arrhythmias, unstable
angina pectoris requiring medication, or clinically significant valvular heart disease.
- - History of pulmonary embolus or deep vein thrombosis diagnosed within the previous
three months.
- - Current uncontrolled medical conditions that could limit a subject's ability to
undertake study therapy.
- - Known or suspected leptomeningeal disease.
- - Inflammatory bowel disease with diarrhea as a major component.
- - Chronic and concomitant use of strong or moderate CYP3A4 inhibitors and strong or
moderate CYP3A4 inducers.
These drugs should be stopped at least 14 days prior to
registration to Step 1.
