Metastatic Breast Cancer, Triple Negative Breast Cancer
Conditions
Keywords
Locally recurrent breast cancer
Brief summary
Patients with metastatic or locally recurrent triple negative breast cancer (TNBC) who are scheduled for medically indicated surgical biopsy or resection of disease will be identified. Fresh/frozen tissue will be collected and will undergo comprehensive molecular evaluation with NextGen sequencing. TGEN's clonal genomics analyses will be applied in the analysis to identify and prioritize the mutated targets. Therapeutic options, based on the genetic profile of each patient's tumor, will be discussed and an appropriate molecularly-selected agent will be recommended by the Study Investigator(s) (SI) and treating oncologist as treatment for the patient. This is an open-label, pilot trial. Patients with metastatic or locally recurrent TNBC who are scheduled for medically indicated surgical biopsy or resection will be enrolled and therapeutic options, based on the genetic profile of each patient's tumor, will be discussed with the patient. Time-to-progression (TTP) for these patients following the selected therapy is the primary objective and will be compared to the TTP(s) for their most recent prior therapy. A 30% increase in TTP with the molecularly-targeted agent compared with the TTP on the immediate prior therapy will be considered as evidence of clinical benefit from the selected therapy. The secondary endpoints are best response to the molecularly-selected therapy, overall survival (OS) and genetic mutation evaluation in metastatic (or locally recurrent) TNBC. The study is designed to demonstrate that the collection and analysis of these tumor samples is feasible.
Interventions
None listed
Sponsors
Translational Drug Development
Life Technologies, Inc.
US Oncology Research
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Has metastatic or locally recurrent triple negative breast cancer and is scheduled for medically indicated surgical biopsy or resection of disease * Will have measurable or evaluable (nonmeasurable) disease per RECIST v 1.1 (see Section 10) present after surgical biopsy/resection. Note: following surgical resection, if the tumor sample is found to be inadequate for comprehensive molecular analysis, the patient will be deemed ineligible and will be replaced. * Has received at least 1 prior chemotherapeutic regimen for their metastatic or locally recurrent TNBC prior to initiating the molecularly-selected therapy. There is no limit on the prior therapy for TNBC. Note: We strongly recommend holding of on intervening therapy if possible from the time of biopsy to the completion of sequencing so as not to change the cancer under the selective pressure of treatment, so that the sequencing results are reflective of the current cancer. * Is at least 18 years of age * Has an expected survival of at least 6 months, as estimated by the treating oncologist * Has planned surgical resection (indicated for the medical care of the patient) that will yield a minimum fresh/frozen tumor sample of 1 cm x 1 cm x 1 cm (\ 300 mg) that will be available for molecular profiling analysis. * Is agreeable to having a blood sample (10-20 mL) drawn and analyzed to compare their normal genetic profile to that of their tumor sample * Has signed the most recent Patient Informed Consent Form * Has signed a Patient Authorization Form
Exclusion criteria
* Has breast cancer other than metastatic or locally recurrent TNBC. Note: surgical resection of the recurrent TNBC will render the patient as no evidence of disease (NED). NED patients are ineligible and will be replaced. * Has a history of heart disease, other conditions that would prevent treatment with a standard chemotherapeutic agent * Has evidence of central nervous system (CNS) involvement that is progressing or that requires radiation, resection or steroid therapy * Has a serious uncontrolled intercurrent medical or psychiatric illness, including serious infection * Is a pregnant or nursing woman * Is unable to comply with requirements of study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Time-to-progression (TTP) | Throughout study, for up to 3 years | Time-to-progression (TTP) for these patients following the selected therapy is the primary objective and will be compared to the TTP(s) for their most recent prior therapy. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Best response | To molecularly selected therapy, for up to 3 years | Best response to therapy selected based on genomic analysis will be determined. Response will be evaluated in this study using the international criteria published by the Response Evaluation Criteria in Solid Tumors (RECIST) Committee v1.1. |
| Overall survival | Throughout the study, for up to 3 years | Survival will be measured, from the selected treatment start date to the date of death or the last date the patient was known to be alive. |
| Genetic mutation evaluation | After surgical resection | Genomic analysis of whole blood and resected tumor will be done |
Countries
United States
Outcome results
None listed