About this trial
Detection of molecular relapse with circulating tumour DNA analysis can identify which patients with ER positive breast cancer are relapsing on adjuvant endocrine therapy. This trial will aim to demonstrate that palbociclib and fulvestrant, can defer or prevent relapse in patients with ctDNA detected molecular relapse.
The TRAK-ER trial will have two phases, a ctDNA surveillance phase and a randomised therapy trial in patients with positive ctDNA.
The TRAK-ER trial will establish a ctDNA screening programme for patients with ER positive breast cancer receiving adjuvant endocrine therapy with at least a further three years of standard adjuvant endocrine therapy planned. Patients recruited into the TRAK-ER study will have high-risk clinical features to identify patients at higher risk of future relapse.
ctDNA assays will be used to identify which people are at very high risk of relapse (i.e. those with a positive ctDNA result), and randomise this high risk population between standard endocrine therapy versus palbociclib plus fulvestrant for up to two years.
Eligibility criteria
Qualifiers
Written informed consent to participate in the trial and to donation of tissue and blood samples
Male or female patients aged 18 years or older
ECOG performance status 0, 1 or 2 (see https://ecog-acrin.org/resources/ecog-performance-status)
Histologically proven primary ER+ (Allred score 6/8 or greater, or stain in ≥10% of cancer cells) and HER2- (immunohistochemistry 0/1+ and/or negative by in situ hybridization) breast cancer as determined by local laboratory
Disqualifiers
Any concurrent or planned treatment for the current diagnosis of breast cancer other than adjuvant endocrine therapy or a bisphosphonate.
Patients with prior exposure to a CDK 4/6 inhibitor as part of standard of care may enrol only after at least 12 months from completing CDK4/6 therapy.
Prior exposure to therapeutic dose of fulvestrant is not permitted. One subtherapeutic dose of fulvestrant is permitted.
Prior diagnosis of cancer including prior diagnosis of breast cancer in the previous 5 years, other than for non-melanoma carcinoma of the skin or cervical carcinoma in situ
Trial design
Treatments tested in this trial
- Palbociclib 125Mg Tab
- Fulvestrant injection
- Tamoxifen
- Letrozole
- Exemestane
- Anastrozole
Treatment groups
Sponsors and collaborators
Royal Marsden NHS Foundation Trust
Lead sponsor
Pfizer
Collaborator
AstraZeneca
Collaborator
Institute of Cancer Research, United Kingdom
Collaborator
UNICANCER
Collaborator
Gustave Roussy, Cancer Campus, Grand Paris
Collaborator
Invitae Corporation
Collaborator