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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Paul Strauss

About this trial

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 criteria

Qualifiers

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

Disqualifiers

Head and neck squamous cell carcinoma accessible to a local treatment

Cancer of nasopharynx, sinus or nasal cavity

Other histology than epidermoid

Patients with contraindication for anti-PD1 immunotherapy

Trial design

Treatments tested in this trial

  • Immunotherapy

Treatment groups

60 Participants
are divided into 1 treatment group

Sponsors and collaborators

Centre Paul Strauss

Lead sponsor

Centre National de la Recherche Scientifique, France

Collaborator

Institut National de la Santé Et de la Recherche Médicale, France

Collaborator