NCT05734950

Brief Summary

This study is investigating the biological characteristics of early oestrogen receptor (ER) positive, human epidermal growth factor receptor 2 (HER2) negative breast cancer (BC) in older woman (aged \> 70 years) who were treated with adjuvant endocrine treatment (ET). It will use surgical tissue previously collected as part of routine care from patients aged 70 years or older at diagnosis with ER positive, HER2 negative stage I-III BC treated The Royal Marsden NHS Foundation Trust (RMH). The overarching aim of this study is to define the biological characteristics of early BC in older women in terms of tumour microenvironment (TME), molecular and genomic features. This analysis will include assessment of tumour infiltrating lymphocytes (TILs), and gene expression profiling with NanoString using the Breast Cancer 360 (BC360TM) assay measuring ribonucleic acid (RNA) expression signatures of genes involved in proliferation, endothelial, angiogenesis, cytotoxicity, stroma, inflammatory chemokines, and apoptosis. This analysis will examine various biological pathways, aiming to inform suitability for certain treatments including cyclin-dependent kinase inhibitors (CDKi), chemotherapy, immunotherapy, or targeted treatments such as phosphoinositide 3-kinases (PI3K) inhibitors, or deoxyribonucleic acid (DNA) damage response.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2022

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 21, 2022

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

February 8, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

February 21, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2023

Completed
Last Updated

February 21, 2023

Status Verified

February 1, 2023

Enrollment Period

1.1 years

First QC Date

February 8, 2023

Last Update Submit

February 8, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Distribution of TILs percentage

    assessed via immunohistochemistry

    August 2023

Secondary Outcomes (2)

  • Gene expression profile patterns across the cohort.

    August 2023

  • Relationship between PAM50, Ki67 (<10% low, ≥ 10% high), PD-L1, modified AIR-CIS

    August 2023

Other Outcomes (1)

  • Association of the molecular features with TTR (Defined as the time from diagnosis (initial biopsy) to local, regional, or distant tumour recurrence or death from breast cancer without prior notification of relapse.).

    August 2023

Interventions

Non-interventional, translational study

Eligibility Criteria

Age71 Years+
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This is a non-interventional, translational study, using surgical tissue (collected as part of routine care) from older women (aged \> 70 years at the time of diagnosis) with early (stage I-III), ER positive, HER2 negative BC who were treated curatively with primary surgery. Patients would not have had any prior treatment with (neo-) adjuvant chemotherapy but received an aromatase-inhibitor in the adjuvant setting.

You may qualify if:

  • Post-menopausal women aged \>70 years at the time of diagnosis of invasive breast cancer.
  • ER positive (Allred score \>5/8), HER2 negative early invasive BC.
  • Stage I-III BC.
  • Surgical tissue available.
  • No pre-surgical systemic therapy (i.e., no pre-operative ET or chemotherapy).
  • Planned adjuvant ET with an aromatase-inhibitor.
  • No adjuvant chemotherapy.
  • Surgery was performed between 1st January 2014 and 31st December 2016.

You may not qualify if:

  • Pre- or perimenopausal.
  • ER negative or HER2-positive BC.
  • Multifocal cancer where not all of foci ER positive HER2 negative
  • Bilateral breast cancer.
  • Stage IV breast cancer.
  • Benign histology or DCIS.
  • Pre-surgical treatment.
  • Prior chemotherapy for BC.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Royal Marsden NHS Foundation Trust

Sutton, SM2 5PT, United Kingdom

Location

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 8, 2023

First Posted

February 21, 2023

Study Start

July 21, 2022

Primary Completion

August 31, 2023

Study Completion

August 31, 2023

Last Updated

February 21, 2023

Record last verified: 2023-02

Data Sharing

IPD Sharing
Will not share

Locations