ClinicalTrials.Veeva

Menu

Heterogeneity of Oral Squamous Cell Carcinoma Analysis by Single Cell RNA Sequencing (HOASIS)

L

Léon Bérard Center

Status

Not yet enrolling

Conditions

Oral Squamous Cell Carcinomas

Treatments

Procedure: Biospecimen
Procedure: Blood sampling

Study type

Interventional

Funder types

Other

Identifiers

NCT06861036
ET22-338 HOASIS

Details and patient eligibility

About

The goal of this project is to characterise the heterogeneity of all cell populations (tumour cells, stromal and immune microenvironment) present in the tumor and their normal (and leucoplasic) counterparts by scRNAseq in OSCC patients.

Full description

Epidermoid carcinomas of upper aerodigestive tract are the 8th most common cancers in the world. Worldwide, this represents more than 500.000 cases per year and 20.000 cases per year in France (statistics 2018-2020). Among these cancers, oral squamous cell carcinoma (OSCC) are the most common location, leading to significant morbidity and mortality.

OSCC treatment is based on surgery and/or radiotherapy and/or chemotherapy. Immune Check point Inhibitors (ICIs) targeting PD-1 have been approved for recurrent and metastasic OSCC. However, only 15-20% of these patients are treated thanks to this anti-PD-1. Thus, there is a real need to improve the efficacy of ICIs in the treatment of HNSCC. The scRNAseq is a method which allows to study the tumoral heterogeneity, the microenvironment and the dynamic and regulation mecanisms in cells cancer. This technology could improve patient stratification, identify pronostic biomarkers, constitute an important tool in the therapeutical take care and lead to understand tumoral evolution and develop new prevention strategies.

The aim of the study is to characterise the heterogeneity of all cell populations (tumour cells, stromal and immune microenvironment) present in the tumor and their normal (and leucoplasic) counterparts by scRNAseq in OSCC patients.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • I1. Male or female at least 18 years old.
  • I2. Patient with OSCC and undergoing surgery at the Centre Léon Bérard.
  • I3. Patient who has agreed to participate in this research and sign consent.
  • I4. Patient affiliated to a medical insurance.

Exclusion criteria

  • NI1. Pregnant or nursing woman.
  • NI2. Contraindication to general anesthesia.
  • NI3. Suspicion of rare tumor of particular histology other than squamous cell carcinoma (Sarcoma...).
  • NI4. Patient under curatorial or guardianship or placed under the protection of justice.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Clinical-biological cohort
Other group
Description:
A clinical-biological cohort of 50 patients with OSCC. Blood sample and biospecimen at the time of a standard surgery.
Treatment:
Procedure: Blood sampling
Procedure: Biospecimen

Trial contacts and locations

1

Loading...

Central trial contact

Philippe Zrounba, M.D.; Karène Mahtouk, Ph.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems