Monitoring luminAl Breast Cancer Through the Evaluation of Mutational and epiGeNEtic alteraTIons of Circulating ESR1 DNA
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hormone Receptor Positive Breast Carcinoma
- Sponsor
- Centro di Riferimento Oncologico - Aviano
- Enrollment
- 164
- Locations
- 7
- Primary Endpoint
- Liquid-biopsy in monitoring treatment response in luminal breast cancer
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
The purpose of the study is to determine the diagnostic role of ctDNA when used to monitor metastatic breast cancer (MBC) during first-line endocrine therapy.
Detailed Description
Patients with hormone receptor-positive MBC are eligible for endocrine therapy (ET) as first line treatment which is based on strategies aimed to either block signaling pathways depending on the estrogen receptor (ESR1) or using ESR1 antagonists. Only a few accepted predictive factors are associated with treatment benefit for MBC (i.e., hormone receptor status and HER2 status). Furthermore, a standardized assessment evaluation for MBC is still lacking. Because of these unmet needs, ET is continued until disease progression, or if toxicity requiring discontinuation occurs. Resistance is frequent in the treatment of early BC and unavoidable in MBC. Recently, mutations in ESR1 have been described in MBC that had been previously exposed to aromatase inhibitors (AIs) and are rarely detectable in primary BC. Besides that, resistance phenomena have been also linked to ESR1 cisregulatory elements (CRE, i.e. enhancers and promoters) hypermethylation, both related to ESR1 silencing. According to the literature, the aim of the study is to detect tumor response with liquid biopsy technique compared to conventional clinical pratice algorithms.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Histologically proven diagnosis of adenocarcinoma of the breast with evidence of metastatic disease.
- •ER positive tumor ≥ 1%
- •HER2 negative breast cancer by FISH or IHC (IHC 0,1+, 2+ and/or FISH HER2: CEP17 ratio \< 2.0)
- •Females, 18 years of age or older
- •Candidate to first-line endocrine therapy (LH-RH analogue for premenopausal women is allowed)
- •Signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all the pertinent aspects of the trial prior to enrollment.
- •Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other trial procedures.
Exclusion Criteria
- •Diagnosis of any secondary malignancy within the last 3 years, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix.
- •Prior endocrine therapy for metastatic disease
Outcomes
Primary Outcomes
Liquid-biopsy in monitoring treatment response in luminal breast cancer
Time Frame: 3 years
The primary objective of this study is to evaluate whether liquid-biopsy technique is able to detect treatment response in luminal breast cancer through the quantification of ESR1 ctDNA mutations
Secondary Outcomes
- Overall Survival (OS)(3 years)
- Treatment resistance mechanisms(3 years)
- Time to Progression (TTP)(3 years)
- ctDNA/miRNA based follow-up(3 years)
- Negative predictive value(3 years)
- Accuracy(6 months)
- Overall Response Rate (ORR)(3 years)
- Positive predictive value(3 years)
- Lead time (for PFS)(3 years)
- Number of futile diagnostic imaging(3 years)
- Specificity(From baseline until disease progression)
- Progression Free Survival (PFS)(3 years)