A Trial of Early Detection of Molecular Relapse With Circulating Tumour DNA Tracking and Treatment With Palbociclib Plus Fulvestrant Versus Standard Endocrine Therapy in Patients With ER Positive HER2 Negative Breast Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorRoyal Marsden NHS Foundation Trust

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

1,100 Participants
are divided into 2 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