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Estrogen Receptor Antagonist

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 (TRAK-ER Trial)

Phase 2
Recruiting
Led By Nicholas Turner
Research Sponsored by Royal Marsden NHS Foundation Trust
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 60 months from randomisation
Awards & highlights
No Placebo-Only Group

Summary

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.

Eligible Conditions
  • Breast cancer
  • Breast Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~60 months from randomisation
This trial's timeline: 3 weeks for screening, Varies for treatment, and 60 months from randomisation for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence of positive ctDNA result at first test (Surveillance phase)
Incidence of positive ctDNA result during surveillance (Surveillance phase)
Relapse free survival (Treatment phase)
Secondary study objectives
Distant recurrence free survival
EQ-5D-5L quality of life assessment: Anxiety/ Depression element
EQ-5D-5L quality of life assessment: Mobility element
+7 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Palbociclib and fulvestrantExperimental Treatment2 Interventions
Treatment with palbociclib plus fulvestrant will continue for a maximum of 24 months. Palbociclib will be given orally once a day on days 1-21 of each 28 day cycle. Fulvestrant 500 mg will be administered on cycle 1 days 1 and 15, cycle 2 day 1 and then every 28 days thereafter (plus or minus 3 days) as two intramuscular injections of 250mg fulvestrant at each visit.
Group II: Standard endocrine therapyActive Control4 Interventions
Standard endocrine therapy will continue for up to 24 months on trial. Standard endocrine therapies include tamoxifen, and aromatase inhibitors (letrozole, anastrazole, exemestane).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Fulvestrant injection
2023
Completed Phase 1
~50

Find a Location

Who is running the clinical trial?

Royal Marsden NHS Foundation TrustLead Sponsor
328 Previous Clinical Trials
10,150,730 Total Patients Enrolled
36 Trials studying Breast Cancer
15,610 Patients Enrolled for Breast Cancer
Institute of Cancer Research, United KingdomOTHER
164 Previous Clinical Trials
131,525 Total Patients Enrolled
25 Trials studying Breast Cancer
26,489 Patients Enrolled for Breast Cancer
AstraZenecaIndustry Sponsor
4,427 Previous Clinical Trials
289,163,352 Total Patients Enrolled
178 Trials studying Breast Cancer
1,245,208 Patients Enrolled for Breast Cancer
PfizerIndustry Sponsor
4,675 Previous Clinical Trials
28,716,082 Total Patients Enrolled
115 Trials studying Breast Cancer
41,383 Patients Enrolled for Breast Cancer
UNICANCEROTHER
233 Previous Clinical Trials
308,737 Total Patients Enrolled
35 Trials studying Breast Cancer
33,740 Patients Enrolled for Breast Cancer
Invitae CorporationIndustry Sponsor
7 Previous Clinical Trials
5,052 Total Patients Enrolled
Gustave Roussy, Cancer Campus, Grand ParisOTHER
264 Previous Clinical Trials
264,896 Total Patients Enrolled
15 Trials studying Breast Cancer
103,373 Patients Enrolled for Breast Cancer
Nicholas TurnerPrincipal InvestigatorRoyal Marsden NHS Foundation Trust
2 Previous Clinical Trials
540 Total Patients Enrolled
1 Trials studying Breast Cancer
400 Patients Enrolled for Breast Cancer
~525 spots leftby Sep 2027