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Clinical Trials in France / NCT07579507
Starting soon Not applicable

Heterogeneity of Oral Carcinogenesis: From PrEneoplasia to Invasive Squamous Cell Carcinoma

NCT07579507 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-06
Last updated
2026-05-12

Condition(s) studied

Oral Squamous Cell CarcinomasOral Potentially Malignant Disorder

Investigational drug(s) / intervention(s)

BiospecimenBlood samplingBiospecimenBiospecimen

Biospecimen: * 1 or 2 tumoral specimen (depending on the size of the tumor). * 1 specimen of the healthy oral mucosa. * 1 OPMD specimen if applicable. The biospecimens will be collected at the time of the surgery organised for the standard routine medical care.

Blood sampling: Blood sampling (6 mL), taken from a routine biological exam.

Biospecimen: * 1 OPMD lesion specimen. * 1 specimen of the healthy oral mucosa (facultative). The biospecimens will be collected during standard routine medical care.

Biospecimen: * 1 cytobrush sample. * 1 OPMD lesion specimen. Samples must be collected in sequence (first the cytobrush, then the biopsy collected during standard routine medical care.).

Study summary

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 OPMD) counterparts by scRNAseq in OSCC patients. Additionally, the study will evaluate the effectiveness of non-invasive cytobrushes as a diagnostic tool compared to traditional biopsies.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * I1: Male or female at least 18 years old. * I2: For Cohort A: patients with OSCC who undergo surgery. For cohorts B and C: patients with OPMD. * I3: Patient who has agreed to participate in this research and sign consent. * I4: Patient affiliated to a medical insurance. * I5: Patient who have not previously received any anticancer treatment (radiotherapy, chemotherapy, or immunotherapy) Exclusion Criteria: * NI1: For cohorts B and C: Patient at high risk of bleeding, such as those receiving anticoagulant or antiplatelet therapy, those with coagulation disorders, or those with a history of severe bleeding within the two weeks prior to enrollment. * NI2: Pregnant or nursing woman. * NI3: Contraindication to general anesthesia. * NI4: Suspicion of rare tumor of particular histology other than squamous cell carcinoma (Sarcoma...). * NI5: Patient under curatorial or guardianship or placed under the protection of justice.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre Léon Bérard Lyon France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07579507 on ClinicalTrials.gov ↗ ← All trials in France