The UK Plasma Based Molecular Profiling of Advanced Breast Cancer to Inform Therapeutic CHoices (plasmaMATCH) Trial

Inclusion Criteria

• •1. Female.
• •2. Aged ≥ 18 years old.
• •3. Histologically confirmed invasive breast carcinoma.
• •4. Metastatic or recurrent locally advanced breast cancer that is not suitable for treatment with radical or curative intent.
• •5. Demonstrated progression of disease by radiological assessment or by clinical assessment within the last 6 weeks.
• •6. Measurable disease by RECIST v1.1.
• •7. Patients must have completed at least one prior line of treatment for advanced breast cancer and/or relapse within 12 months of completing (neo)adjuvant chemotherapy. Patients with HER2 positive breast cancer must have been treated with at least two courses of HER2 targeted therapy in the advanced setting (or one course if no further courses of HER2 targeted therapy are available locally).
• •8. Patient must either be suitable for a baseline biopsy of recurrent disease or have an archival biopsy of recurrent disease available. Patients are requested to consent to a baseline biopsy but if deemed unsafe by the Investigator, an archival biopsy of recurrent disease can be used instead. If it is deemed unsafe to proceed with baseline biopsy, and no archival recurrent disease biopsy is available, the patient will not be eligible for entry into the treatment cohort.
• •9. ECOG performance status ≤ 2.
• •10. Life expectancy \>3 months in Cohorts A-D, \>16 weeks in Cohort E.
• •11. Patients must be a) surgically sterile; b) have a sterilised sole partner; c) be postmenopausal; d) must agree to practice true abstinence; or e) must agree to use effective contraception during the period of trial treatment and be willing to do so for 6 months following the end of trial treatment. Effective contraception is defined as double barrier contraception (e.g. condom plus spermicide in combination with a diaphragm, cervical cap or intrauterine device). Ovarian suppression with an LHRH agonist is not a method of contraception.
• •12. Patients of childbearing potential should have a negative serum pregnancy test within 14 days prior to initiation of trial treatment.
• •13. At least 4 weeks washout period after the end of trial treatment on a different cohort within plasmaMATCH.
• •14. Adequate haematological, renal and hepatic function as defined by cohort-specific criteria in protocol.
• •15. For patients with ER positive breast cancer in Cohorts A, B and C: EITHER postmenopausal, as defined by at least one of the following criteria: Age \>60 years; Age \<60 years and cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; and serum estradiol and follicle stimulating hormone (FSH) level within the laboratory's reference range for postmenopausal females; Documented bilateral oophorectomy; medically confirmed ovarian failure. OR Pre-/peri-menopausal (i.e. not meeting the criteria for being postmenopausal) if being treated with an LHRH agonist that was commenced at least 4 weeks prior to Cycle 1 Day 1, and continues on the LHRH agonist throughout the trial period.
• •NB. Additional eligibility criteria apply for entry into each treatment cohort.