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Feasibility Study on the Characterization of the Immune Profile of Young Patients After Treatment for Breast Cancer

Feasibility Study on the Characterization of the Immune Profile of Young Patients After Treatment for Breast Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04645849
Acronym
C-PiACs
Enrollment
26
Registered
2020-11-27
Start date
2020-06-15
Completion date
2021-11-30
Last updated
2020-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Immunity recovery, post treatment

Brief summary

This study aim to determine kinetic of post treatment recovery/variation of a panel of innate and adaptative immune system cells and molecules. The results should allow to determine the optimal post treatment immunomonitoring timing and panel to be used for future studies.

Detailed description

There is a complexe interaction between tumor cells ans host immunity. Immunity system (IS) is clearly involved in cancer developement control, and it is suggested that it could participate to the response to anti cancer treatment. There is however no validated immunomonitoring strategy to allow a reliable patient's immune status along time, and particularly after treatment.There are scarce existing information on immunologic reconstitution profile recovery after treatment. This study aim to perform immunomonitoring in young patients with cancer to describe kinetic of recovery/variation of a panel of innate and adaptative immune system cells and molecules, selected by their potential relevance according to literature. The concerned population are young women (˂40 yo) with breast cancer. There will be 2 patients cohorts A or End of treatment : patients recruited at the end of treatment (study cohort) B or Diagnosis : Patients recruited at diagnosis (reference values) This study should contribute to give sufficient data to determine the pertinent timing and cells/molecules panel to evaluate immunity profiling after treatment. These results could be used for further studies.

Interventions

16 patients will be recruited at the end of treatment: an immunoprofiling analysis will be performed out of a blood sample about 1 month, 5 months and 9 months after treatment. 8 patients will be recruited at diagnosis: a immune profile analysis will be performed before the start of treatment. This will give comparative values for the immune system cells and molecules.

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* Women with Breast cancer at initial diagnosis OR at the end of treatment * Chemotherapy planned or performed in the treatment plan * Patient not opposed to participate to the present study * Affiliated to a French social security scheme.

Exclusion criteria

* metastatic breast cancer * pregnant or breastfeeding woman * Treatment with monoclonal antibodies or immunotherapy * Immunosuppressive therapy * Thymus irradiation * Chronic infection in progress * Inborn or acquired disease (other than breast cancer) impacting the immune system (SAA, Lupus…) * Subject under guardianship or deprived of liberty

Design outcomes

Primary

MeasureTime frameDescription
Identification of the relevant biological parameters of the innate / adaptive immune system15 monthsAnalysis of immune profile implies to evaluate changes of about 30 distinct immune cell (sub)types with their activation markers. These analyses are conducted at 3 time points for cohort A or End of treatment (1, 5, 9 months) and once for cohort B or Diagnosis before treatment start : -% and counts of immune cell populations (B-lymphocytes, T-lymphocytes, dendritic cells) * activation levels of cell subpopulations * Secretion of cytokines after activation * Determination of cytokines and chemokines after activation (picograms/ml) Description of the evolution of the parameters measured for cohort A or End of treatment with comparison to normal values (data from the EFS cohort and from cohort B or Diagnosis) Analysis of the reconstitution kinetic should allow us to determine wich biological parameters (immune cell (sub)types and their activation markers) will be most relevant to study immune profile reconstitution for further studies.

Secondary

MeasureTime frameDescription
Analysis feasibility15 monthsnumber of samples analysed versus planned, quality of the results
Immunity Cells and molecules kinetic analysis15 monthsThe objective is to determine the best moment for analysis of immune system reconstitution (cf outcome 1 measures) For each patient, and each immune system marker tested (cells/molecules): kinetic analysis of return to values comparable to reference values (data from the EFS = french blood establishment and the 8 patients tested before the start of treatment).

Countries

France

Contacts

Primary ContactLeila Gofti-Laroche, PharmD
LGofti-laroche@chu-grenoble.fr0033 4 76 76 68 74

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026