A Study to Measure the Expression of the HER2-HER3 Dimer in Tumour and Blood (Exosomes) Samples From Patients With HER2 Positive Breast Cancer Receiving HER2 Targeted Therapies

NCT04288141 | Unknown

• 1 other identifier: HERdi PREDICT
• Study Type: observational
• Target: 40
• Locations: 1 country
• Sites: 2

Brief Summary

The treatment of breast cancer is determined by its 'receptor (or signal) status'. Receptors are signals present on all cells and if abnormal can drive cancer growth. One of the signals that can drive breast cancer growth is the HER2 receptor/signal. One quarter of all breast cancers are found to have too many HER2 signals i.e. HER2-positive breast cancer. HER2 is a member of the HER-family which constitutes HER1,HER2,HER3,and HER4 signals. Currently, tests can identify breast cancers with too much HER2, from a biopsy, so a cancer doctor can prescribe anti-HER2 treatment to block these signals. These drugs have improved survival rates in HER2-positive breast cancer. Members of the HER family can also 'pair' with each other to activate signals that encourage cancer growth. For example, HER3 naturally 'pairs' with HER2. Though anti-cancer drugs have been developed to target this pairing, the current method of patient selection is not developed to detect pairing of signals in tissue biopsies. A specialist imaging technique called FLIM-FRET (FLIM- Fluorescence Lifetime Imaging Microscopy; FRET- Forster resonance energy transfer) can identify signal pairing on cancer cells from tissue, and potentially, from blood samples. This study involves having blood tests while participants receive anti-HER2 treatment. The investigators will also seek permission to take samples of cancer tissue from the biopsies that were already carried out, e.g. at diagnosis. Some participants may need an additional biopsy, which will be discussed with participants prior to consent. This study will use the specialist FLIM-FRET technique to measure the signal pairing in tumour samples and blood samples. Investigators will measure if the levels of signal pairing from blood are the same as that from tissue, which could lead to bloods tests being used to select patients for anti-HER2 treatments, instead of invasive tissue biopsies. Changes in signal pairing may also help to predict if a cancer is becoming resistant to treatment.

Conditions

HER2-positive Breast Cancer

Keywords

FLIM-FRET; HER2-HER3 dimer; Exosomes; Predictive biomarkers

Outcome Measures

Primary Outcomes (1)

• Compare HER2-HER3 dimer expression as detected by FLIM-FRET (% positive for HER2-HER3 dimer expression with FRET efficiency ≥8.56%) to HER2 over-expression (% positive for HER2 over-expression by IHC ± FISH) in patient-derived tumour samples.

  Group 1: Baseline biopsy and definitive surgical specimen. Group 2: Baseline biopsy.

Secondary Outcomes (9)

• Describe the range of FRET efficiency determined by measuring tumoural HER2-HER3 dimerisation as a continuous variable.

  Group 1: Baseline biopsy and definitive surgical specimen. Group 2: Baseline biopsy.

• Compare the HER2-HER3 dimer expression level in tumour samples to matched blood samples (exosomal expression) as detected by FLIM-FRET.

  Each cycle (C) is 21 days (D). Group 1A & Group 1B: Baseline biopsy,definitive surgical specimen and paired blood samples. Group 1A: Also in matched interim tumour and blood sample (C4 D14-21). Group 2: Baseline biopsy and blood sample

• Compare HER2 expression in blood samples (exosomes) by protein detection assays e.g. dot blots to HER2 status in matched tumour tissue as determined by IHC ± FISH.

  Each cycle (C) is 21 days (D). In group1 HER2 expression in matched participant tumour tissue and blood will be compared at baseline and immediately after completion of neoadjuvant therapy/surgery. In Group 2, to be assessed at baseline only.

• Determine the range of measurable exosomal FRET efficiency determined by measuring exosomal HER2-HER3 dimer expression.

  Each cycle (C) is 21 days (D). In group1a: Baseline, C2 D1, C5 D1, C6 D1 and C8 D21-42. In Group 1b: Baseline, C2 D1, C6 D21-42, Group 2: Baseline, C2 D1, C4/5 D1.

• Determine if patient derived tumour and blood samples (exosomes) demonstrate a change in HER2-HER3 dimer expression in response to systemic HER2-directed therapy (% positive for change in HER2-HER3 dimer expression).

  Each cycle (C) is 21 days (D). In group1a: Baseline, C2 D1, C5 D1, C6 D1 and C8 D21-42. In Group 1b: Baseline, C2 D1, C6 D21-42, Group 2: Baseline, C2 D1, C4/5 D1. In tumour at baseline, C4 D14-21 (group 1a only) & immediately after surgery(group 1 only)

Study Arms (2)

Group 1: Early HER2 positive breast cancer

Study participants in Group 1 will include patients prescribed neoadjuvant systemic therapy (including trastuzumab and pertuzumab) by their treating oncologist for a diagnosis of HER2 positive early breast cancer.

Other: Acquisition of blood samples and tumour tissue samples (biopsies)

Group 2: Metastatic HER2 positive breast cancer

Study participants in Group 2 will include patients prescribed systemic therapy (including trastuzumab and pertuzumab) by their treating oncologist for a diagnosis of HER2 positive metastatic breast cancer.

Other: Acquisition of blood samples and tumour tissue samples (biopsies)

Interventions

Acquisition of blood samples and tumour tissue samples (biopsies) OTHER

Acquisition of blood samples and tumour tissue samples (biopsies) in a sequential manner as participants proceed through HER2-directed therapy as prescribed by their oncologist.

Group 1: Early HER2 positive breast cancer; Group 2: Metastatic HER2 positive breast cancer

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Group 1: Early HER2 positive breast cancer and prescribed neoadjuvant chemotherapy including trastuzumab and pertuzumab as per physician discretion. Group 2: Metastatic HER2 positive breast cancer and prescribed chemotherapy including trastuzumab and pertuzumab as per physician discretion.

You may qualify if:

• Female or Male aged 18 years or above.
• HER2 positive breast cancer, to be established by immunohistochemistry and confirmed by fluorescence in situ hybridisation or dual in situ hybridisation in borderline cases as per standard of care guidelines.
• Confirmation of availability of sufficient tumour tissue (from diagnostic core biopsy) for biomarker analysis (Refer to study laboratory manual)
• Fit for treatment with chemotherapy in combination with HER2 targeted therapy as per investigator discretion
• Life expectancy of 12 weeks or more.
• Participant is willing and able to give informed consent for participation in the study and in the investigator's opinion, is able and willing to comply with all study requirements.
• Participant willing to undergo additional biopsies when required i.e. Group 1A and Group 2
• Willing to allow his or her general practitioner to be notified of participation in the study \[optional\].
• Group 2 specific criteria
• The pre-treatment tumour sample for biomarker analysis in group 2 will be acquired from the diagnostic biopsy acquired when participants were first diagnosed with metastatic HER2 positive breast cancer. The biopsy should have been acquired following or at the time of the diagnosis of metastatic breast cancer (i.e. cannot use tumour tissue acquired during a prior diagnosis of early/locally advanced breast cancer for this study's biomarker analysis). The biopsy may be acquired from a breast mass or a metastatic site. If a biopsy following or at the time of the diagnosis of metastatic breast cancer has not been carried out, a study specific biopsy will need to be organised.
• Only patients recommended first line treatment with a taxane, trastuzumab and pertuzumab by their physician, are eligible. Potential participants being considered for treatment with any other treatment combinations with HER2 targeted therapies will not be considered eligible.

You may not qualify if:

• Significant thrombocytopaenia or abnormal clotting screen or any other condition that would contraindicate a tissue biopsy if this were required, in the investigator's opinion.
• Participant unwilling to undergo study required tissue biopsies and blood sampling.
• Any other significant underlying condition or comorbidity which, in the opinion of the investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study or the participant's ability to participate in the study.
• Inability of participant to co-operate with study procedures as judged by the investigator.

Sponsors & Collaborators

• King's College London: lead
• Guy's and St Thomas' NHS Foundation Trust: collaborator
• Brighton and Sussex University Hospitals NHS Trust: collaborator

Study Sites (2)

Brighton and Sussex University Hospitals NHS Trust

Brighton, BN2 5BB, United Kingdom

NOT YET RECRUITING

Guy's Cancer Centre, Guy's and St Thomas' NHS Foundation Trust

London, SE1 9RT, United Kingdom

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Participant derived tumour samples, exosomes (extracted from serum samples), Peripheral blood mononuclear cells (PBMCs) and plasma

MeSH Terms

Interventions

Biopsy

Intervention Hierarchy (Ancestors)

Cytodiagnosis; Cytological Techniques; Clinical Laboratory Techniques; Diagnostic Techniques and Procedures; Diagnosis; Specimen Handling; Diagnostic Techniques, Surgical; Surgical Procedures, Operative; Investigative Techniques

Central Study Contacts

Louisa McDonald

CONTACT

0207 188 2007; Louisa.McDonald@gstt.nhs.uk

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 14, 2020
• First Posted: February 28, 2020
• Study Start: December 20, 2019
• Primary Completion: June 1, 2023
• Study Completion: June 1, 2023
• Last Updated: November 14, 2022

Record last verified: 2022-11

Data Sharing

• IPD Sharing: Will not share

Locations

GB (2)