MACSSI (MAstectomie Cellules Souches Surveillance Immunitaire) (MACSSI)

January 24, 2024 updated by: Centre Leon Berard

Evaluation of Stem and Immune Cells in the Early Stage Breast Cancer Without Genetic Risk

Monocentric, observational and prospective study in adult women having an early-stage breast cancer without genetic risk.

The main objective is to characterize quantitatively and qualitatively, after solitary confinement, the resident breast stem cells and the immune system cells infiltrated in the mammary gland in women:

  • With a moderate risk of breast cancer progression (women with an early "Luminal A" tumor) = Group A.
  • With a high risk of breast cancer progression (women with an early "Luminal B" or basal tumor) = Group B.

Study Overview

Detailed Description

Breast cancer is one of the most frequent and the second cause of mortality for women in the world. Breast is a complex organ which has several changes (puberty, pregnancy and menopause). These modifications are controlled by numerous signals as those transmitted by the oestrogens. They are possible through the presence of stem cells in the mammary gland which are able to reply to these signals and can be the target of alterations leading to cancer cells occurence. Breast tumors are composed of complex entities of different kinds of cancer and normal cells which constitute the tumor micro-environment including the immune system cells. This micro-environment transmits a lot of signals to cancer cells and particularly stem cells which can contribute to their survival, the tumor progression and interfere with the treatments efficacy.

The detection of the major deregulation of BMP2 synthesis by mammary micro-environment cells may be a reliable and early biomarker of carcinogens exposure and an indicator of a high risk of developing a luminal type breast cancer.

The immune micro-environment, which has an impact on solid cancer patients' survival, should be taken into consideration for new therapeutic strategies.

Some infiltrating tumour immune cells, as macrophages (TAM) or regulating T and B cells, have shown their key role in tumour escape and metastases apparition. It is relevant to associate the evaluation of immune infiltrate to the breast stem cells in early stage tumours since the literature suggests a functional interaction of these two cellular compartments, particularly in the glioblastoma and the prostate cancer. It seems that mammary stem cells are a major element in the comprehension of breast carcinogenesis but also in the possibilities of repairing the mammary tissue controlling the mammary carcinogenesis.

It is fundamental to clarify the role of stem cells and immunity. Our hypothesis is that breast stem cells are altered in women having a high risk of cancer progression. They would be responsible for a reduced activity of cellular repair and/or contribute to tumour development.

MACSSI project consists in isolating, quantifying and characterizing the breast stem cells and the isolated immune cells of samples obtained for the prophylactic mastectomy in women presenting different tumour progression risks.

The results will be compared to normal samples already collected in women who had a breast reduction.

Study Type

Observational

Enrollment (Estimated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Adult women having an early-stage breast cancer without genetic risk requiring a breast surgery

Description

Inclusion Criteria:

  • Age ≥ 18 years
  • Patient requiring a breast surgery (total mastectomy) of an early stage tumour classified as :

    • Luminal A (Arm A) : Patients with a moderate risk of breast cancer progression or,
    • Luminal B or Basal (Arm B) : Patients with a high risk of breast cancer progression
  • Systemic treatment not initiated
  • Breast cup size ≥ C
  • Informed and signed consent.

Exclusion Criteria:

  • Neo-adjuvant chemotherapy or hormonotherapy
  • History of breast irradiation
  • Pregnant or breastfeeding woman
  • Patient under tutorship or curatorship
  • Patient who underwent a lumpectomy with a level-2 oncoplastic surgery (ex: breast reduction with an inverted-T remodeling)
  • Any other prior anti-tumor treatment
  • Other medical pathology which may interfere with the biologic evaluation, especially chronic auto-immune diseases.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To characterise quantitatively and qualitatively, after solitary confinement, the resident breast stem cells and the immune system cells infiltrated in the mammary gland according to the risk of breast cancer progression (group A and B)
Time Frame: Within one month after inclusion (date of surgery)
Rate of stem and immune cells and phenotype analysis
Within one month after inclusion (date of surgery)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional characterization, after solitary confinement, of stem cells and immune system cells from groups A and B
Time Frame: Within one month after inclusion (date of surgery)
Functional test: mammosphere
Within one month after inclusion (date of surgery)
Functional characterization, after solitary confinement, of stem cells and immune system cells from groups A and B
Time Frame: Within one month after inclusion (date of surgery)
Functional test: TDLU
Within one month after inclusion (date of surgery)
Functional characterization, after solitary confinement, of stem cells and immune system cells from groups A and B
Time Frame: Within one month after inclusion (date of surgery)
Functional test: E-CFC - FACS
Within one month after inclusion (date of surgery)
Determination of the stem cells role in the cellular regulation and repair activity
Time Frame: Within one month after inclusion (date of surgery)
Functional tests
Within one month after inclusion (date of surgery)
Determination of the efficacy of the immune systems cells found in the samples in the early stage of breast tumorigenesis
Time Frame: Within one month after inclusion (date of surgery)
FACS
Within one month after inclusion (date of surgery)
Evaluation of the role of breast stem and immune cells in the early stage development of a breast cancer: risk or protective factor ?
Time Frame: Within one month after inclusion (date of surgery)
Functional tests: mammosphere, TDLU, E-CFC - FACS
Within one month after inclusion (date of surgery)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: DELAY Emmanuel, MD, Centre léon bérard

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 22, 2021

Primary Completion (Estimated)

February 22, 2024

Study Completion (Estimated)

November 15, 2024

Study Registration Dates

First Submitted

September 25, 2018

First Submitted That Met QC Criteria

March 8, 2019

First Posted (Actual)

March 12, 2019

Study Record Updates

Last Update Posted (Actual)

January 25, 2024

Last Update Submitted That Met QC Criteria

January 24, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • MACSSI (ET18-150)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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