Biological Characteristics of Older Women (> 70 Years) With ER Positive, HER2 Negative Early Breast Cancer
BOLD-70
1 other identifier
observational
100
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 21, 2022
CompletedFirst Submitted
Initial submission to the registry
February 8, 2023
CompletedFirst Posted
Study publicly available on registry
February 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2023
CompletedFebruary 21, 2023
February 1, 2023
1.1 years
February 8, 2023
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
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
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