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Spots Global Cancer Trial Database for Feasibility Study on the Characterization of the Immune Profile of Young Patients After Treatment for Breast Cancer

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Trial Identification

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

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

Study ID: NCT04645849

Conditions

Breast Cancer

Interventions

Immunomonitoring

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Chu Grenoble Alpes, Grenoble, , France

Contact Details

Name: Leila Gofti-Laroche, PharmD

Affiliation: University Hospital, Grenoble

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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