Phenotypic, Functional, Metabolic and Transcriptomic Profiling of Circulating Immune Cells to Uncover Response Signatures to Anti-PD1 Immunotherapy in Melanoma Patients

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Despite being standard of care, there are still many medical requirements related to immune checkpoint blocker based therapies such as identify patients susceptible to respond with the less adverse events, evaluate the clinical benefit of adjuvant treatment /risk of relapse and design new strategies for non-responder patients. Thus, this project aims at understanding the impact of anti-PD1 on the immune system through investigation of the phenotypic, functional, metabolic and transcriptomic profiles of circulating DC subsets and effectors in response to anti-PD1 therapy in melanoma patients. The primary objective of the study is to identify the biomarkers of response to anti-PD1 according to the type of patient before the start of the treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient with histologically confirmed melanoma (stage I, II, III or IV based on AJCC classification)

• Able to sign the informed collection consent for the retrospective part or to express their non-opposition to the research for the prospective part of the study

Locations
Other Locations
France
CHU Grenoble Alpes
RECRUITING
Grenoble
Contact Information
Primary
Julie Charles, MD, PhD
jcharles@chu-grenoble.fr
476769320
Backup
Stéphane Mouret, PhD
smouret1@chu-grenoble.fr
476767081
Time Frame
Start Date: 2024-01-17
Estimated Completion Date: 2031-01
Participants
Target number of participants: 707
Treatments
Cohort #A
monotherapy anti-PD1 first line
Cohort #B
monotherapy anti-PD1 second line
Cohort #C
monotherapy anti-PD1 adjuvant
Cohort #D
combotherapy anti-PD1/CTLA-4 first line
Cohort #E
untreated stage I and II melanoma patient
Related Therapeutic Areas
Sponsors
Collaborators: Etablissement Français du Sang
Leads: University Hospital, Grenoble

This content was sourced from clinicaltrials.gov