INSTIGO: Evaluation of a Plasma Protein Profile as a Predictive Biomarker for Metastatic Relapse in Triple Negative Breast Cancer Patients

Sponsor
Centre Jean Perrin (Other)
Overall Status
Recruiting
CT.gov ID
NCT04438681
Collaborator
(none)
90
1
107.4
0.8

Study Details

Study Description

Brief Summary

The INSTIGO study aims to assess a plasma protein profile at different stages of patient follow-up as a predictive factor of metastatic recurrence in triple negative breast cancer. It also aims to look at other potential biomarkers of metastatic relapse such as Tumor-infiltrating Lymphocytes, circulating tumor DNA, figurative elements in blood, or a tumor RNA signature.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The investigators propose to carry out a study that measures the concentrations of a set of plasma proteins in order to assess their ability to predict metastatic relapse of triple negative breast cancer. A plasma protein profile could be an interesting biomarker since it is easily accessible and quantifiable.

    The investigators also propose to search relation between metastatic relapse in TNBC and other biomarkers or potential biomarkers such as Tumor-infiltrating Lymphocytes (TILs), figurative blood components and circulating tumour DNA (ctDNA).

    Finally, they also want to validate a TNBC RNA signature, established at Jean PERRIN Center, by analyzing the RNA expression of 8 genes.

    Before treatment begins, the patient will take an initial blood sample. A second blood sample will be taken on the day of the first surgery or the day of the surgery post chemotherapy. A third blood sample will be done on the day of the beginning of the radiotherapy. A 4th and a 5th blood sample will be done at 6 months and 1 year respectively after the end of the radiotherapy. A part of these blood samples will be used for the quantification of circulating proteins, for the determination of the blood's figurative elements and for the quantification of circulating tumour DNA.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    90 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    INSTIGO Trial: Evaluation of a Plasma Protein Profile as a Predictive Biomarker for Metastatic Relapse in Triple Negative Breast Cancer Patients
    Actual Study Start Date :
    Nov 27, 2020
    Anticipated Primary Completion Date :
    Nov 9, 2023
    Anticipated Study Completion Date :
    Nov 9, 2029

    Outcome Measures

    Primary Outcome Measures

    1. Identification at diagnosis of a plasma protein profile predictive of metastatic relapse in patients with triple-negative breast cancer (TNBC) [8 years]

      - Plasma concentrations of a set of proteins at diagnosis (measured in g/L)

    2. Identification at diagnosis of a plasma protein profile predictive of metastatic relapse in patients with triple-negative breast cancer (TNBC) [8 years]

      - Time to metastatic relapse

    Secondary Outcome Measures

    1. Identification of a plasma protein profile predictive of metastatic relapse in patients with TNBC : on the day of primary surgery or post-chemotherapy surgery, the day the radiotherapy begins, at 6 months after radiotherapy and one year post-radiotherapy [8 years]

      - Plasma concentrations of a set of proteins (measured in g/L)

    2. Identification of a plasma protein profile predictive of metastatic relapse in patients with TNBC : on the day of primary surgery or post-chemotherapy surgery, the day the radiotherapy begins, at 6 months after radiotherapy and one year post-radiotherapy [8 years]

      - Time to metastatic relapse

    3. Identification of a characteristic plasma protein profile at the time of metastatic relapse [8 years]

      - Plasma concentrations of a set of proteins (measured in g/L)

    4. Evaluation of the relationship between the rate of tumour lymphocyte infiltration at diagnosis and metastatic relapse. [8 years]

      - Tumor lymphocyte infiltration rate before treatment

    5. Evaluation of the relationship between ctDNA plasma levels and metastatic disease relapse [8 years]

      - Measurement of plasma ctDNA level

    6. Evaluation of the relationship between ctDNA plasma levels and metastatic disease relapse [8 years]

      - Time to metastatic relapse

    7. Evaluation of the relationship between Platelet-to-lymphocyte Ratio (PLR) and Neutrophil-to-lymphocyte Ratio (NLR) and metastatic relapse [8 years]

      - The values of NLR and PLR at diagnosis (no Unit)

    8. Evaluation of a metastatic relapse prognostic RNA signature for triple negative breast tumors [8 years]

      - RNA expression of 6 genes of interest

    9. Identification at diagnosis of a plasma protein profile predictive of response to neoadjuvant chemotherapy [3 years and 6 months]

      - Plasma concentrations of a set of proteins at diagnosis

    10. Identification at diagnosis of a plasma protein profile predictive of response to neoadjuvant chemotherapy [3 years and 6 months]

      - Histological response according to the Sataloff classification

    11. Evaluation of the relationship between the rate of tumour lymphocyte infiltration at diagnosis and the response to a neoadjuvant chemotherapy . [3 years and 6 months]

      - Tumor lymphocyte infiltration rate before treatment

    12. Evaluation of the relationship between Platelet-to-lymphocyte Ratio (PLR) and Neutrophil-to-lymphocyte Ratio (NLR) and the response to a neoadjuvant chemotherapy [3 years and 6 months]

      The values of NLR and PLR at diagnosis The values of NLR and PLR after neoadjuvant chemotherapy

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Female

    • Age > 18 years

    • Diagnosed with primitive, non-metastatic, histologically proved, triple negative breast cancer

    • Patient able to understand the French language

    • Patient affiliated to social security

    • Obtaining signed written consent

    Exclusion Criteria:
    • Persons deprived of their freedom or under guardianship or incapable of giving consent

    • Refusal to participate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centre Jean PERRIN Clermont-Ferrand France 63011

    Sponsors and Collaborators

    • Centre Jean Perrin

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centre Jean Perrin
    ClinicalTrials.gov Identifier:
    NCT04438681
    Other Study ID Numbers:
    • 2020-A01423-36
    First Posted:
    Jun 19, 2020
    Last Update Posted:
    Jan 13, 2022
    Last Verified:
    Jan 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 13, 2022