Phase 3
N=431
A Study Evaluating Talazoparib (BMN 673), a PARP Inhibitor, in Advanced and/or Metastatic Breast Cancer Patients With BRCA Mutation (EMBRACA Study)
Breast Neoplasms · BRCA 1 Gene Mutation · BRCA 2 Gene Mutation
Bottom Line
View on ClinicalTrials.gov: NCT01945775 ↗Enrolled (actual)
431
Serious AEs
34.5%
Results posted
Oct 2018
Primary outcome: Primary: Progression-Free Survival (PFS): Independent Radiological Facility (IRF) Assessment — 8.6; 5.6 months — p=<0.0001
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- talazoparib (Drug); Physician's-Choice (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Pfizer
- Primary completion
- Sep 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Progression-Free Survival (PFS): Independent Radiological Facility (IRF) Assessment |
8.6; 5.6 | <0.0001 sig |
| SECONDARY Percentage of Participants With Objective Response: Investigator Assessment |
62.6; 27.2 | <0.0001 sig |
| SECONDARY Overall Survival (OS) |
19.3; 19.5 | 0.1693 |
| SECONDARY Trough Plasma Talazoparib Concentrations |
3370; 3570; 3400 | — |
| SECONDARY Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) |
282; 123; 103; 39 | — |
| SECONDARY Number of Participants With Grade 3 or 4 Post-baseline Toxicities in Laboratory Parameters: Hematology |
115; 8; 43; 31; 54; 11 | — |
| SECONDARY Number of Participants With Grade 3 or 4 Post-baseline Toxicities in Laboratory Parameters: Chemistry |
5; 3; 6; 2; 7; 4 | — |
| SECONDARY Number of Participants With Potentially Clinically Significant Changes From Baseline in Vital Signs |
3; 2; 8; 2; 0; 0 | — |
| SECONDARY Number of Participants Taking At-least One Concomitant Medication |
281; 126 | — |
Summary
The purpose of this open-label, 2:1 randomized phase III trial is to compare the safety and efficacy of talazoparib (also known as BMN 673) versus protocol-specific physician's choice in patients who have locally advanced and/or metastatic breast cancer with germline BRCA mutations.
Eligibility Criteria
Inclusion Criteria
- Histologically or cytologically confirmed carcinoma of the breast
- Locally advanced breast cancer that is not amenable to curative radiation or surgical cure and/or metastatic disease appropriate for systemic single cytotoxic chemotherapy
- Documentation of a deleterious, suspected deleterious, or pathogenic germline BRCA1 or BRCA2 mutation from Myriad Genetics or other laboratory approved by the Sponsor
- No more than 3 prior chemotherapy-inclusive regimens for locally advanced and/or metastatic disease (no limit on prior hormonal therapies or targeted anticancer therapies such as mechanistic target of rapamycin (mTOR) or CDK4/6 inhibitors, immune-oncology agents, tyrosine kinase inhibitors, or monoclonal antibodies against CTL4 or VEGF)
- Prior treatment with a taxane and/or anthracycline in the neoadjuvant, adjuvant, locally advanced, or metastatic setting unless medically contraindicated
- Have measurable or non-measurable, evaluable disease by the revised response evaluation criteria in solid tumors (RECIST) v.1.1
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
Exclusion Criteria
- First-line locally advanced and/or metastatic breast cancer with no prior adjuvant chemotherapy unless the Investigator determines that one of the 4 cytotoxic chemotherapy agents in the control arm would otherwise be offered to the subject
- Prior treatment with a PARP inhibitor (not including iniparib)
- Not a candidate for treatment with at least 1 of the treatments of protocol-specific physician's choice (ie, capecitabine, eribulin, gemcitabine, vinorelbine)
- Subjects who had objective disease progression while receiving platinum chemotherapy administered for locally advanced or metastatic disease; subjects who received low-dose platinum therapy administered in combination with radiation therapy are not excluded
- Subjects who have received platinum in the adjuvant or neoadjuvant setting are eligible; however, subjects may not have relapsed within 6 months of the last dose of prior platinum therapy
- Cytotoxic chemotherapy within 14 days before randomization
- Radiation or anti-hormonal therapy or other targeted anticancer therapy within 14 days before randomization
- HER2 positive breast cancer
- Active inflammatory breast cancer
- CNS metastases
- Exception: Adequately treated brain metastases documented by baseline CT or MRI scan that has not progressed since previous scans and that does not require corticosteroids (except prednisone ≤ 5 mg/day or equivalent) for management of CNS symptoms. A repeat CT or MRI following the identification of CNS metastases (obtained at least 2 weeks after definitive therapy) must document adequately treated brain metastases.
- Subjects with leptomeningeal carcinomatosis are not permitted
- Prior malignancy except for any of the following:
- Prior BRCA-associated cancer as long as there is no current evidence of the cancer
- Carcinoma in situ or non-melanoma skin cancer
- A cancer diagnosed and definitively treated ≥ 5 years before randomization with no subsequent evidence of recurrence
- Known to be human immunodeficiency virus positive
- Known active hepatitis C virus, or known active hepatitis B virus
- Known hypersensitivity to any of the components of talazoparib
Data sourced from ClinicalTrials.gov (NCT01945775). 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.