Identification of Predictive Factors for the Response to Anti-Programmed Cell Death Protein 1 (PD1) Immunotherapy in Head and Neck Squamous Cell Carcinoma

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

This project aims to organise the sampling of blood and tumor at key points of the standard of care of patients with recurrent or metastatic squamous-cell carcinoma of the head and neck (HNSCC). This will allow to identify new potential predictive biomarkers of efficacy of immunotherapy and to investigate the evolution of the tumoral microenvironment after successive systemic treatments.

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

• Patients with recurrent squamous-cell carcinoma of the head and neck not amenable to local therapy and/or with metastatic disease

• Tumor directly accessible to clinical examination (tumor of oral cavity and of oropharynx) and/or cervical lymphadenopathy accessible to echography allowing to realise biopsy under local anesthesia

• Indication to treatment by anti-PD1 immunotherapy according to French competent authority recommendations

• Performance status 0, 1 or 2

• At least one measurable lesion on RECIST V1.1 criteria

Locations
Other Locations
France
Institut de cancérologie Strasbourg Europe
RECRUITING
Strasbourg
Contact Information
Primary
Valérie SARTORI
promotion-rc@icans.eu
03 68 33 95 23
Backup
Manon VOEGELIN
promotion-rc@icans.eu
03 68 33 95 23
Time Frame
Start Date: 2023-08-25
Estimated Completion Date: 2029-08-25
Participants
Target number of participants: 60
Treatments
Recurrent and/or metastatic head and neck carcinoma
Patients with indication of anti-PD1 immunotherapy according to recommendations
Sponsors
Collaborators: Institut National de la Santé Et de la Recherche Médicale, France, Centre National de la Recherche Scientifique, France
Leads: Institut de cancérologie Strasbourg Europe

This content was sourced from clinicaltrials.gov

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