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Recruiting Observational

Follow-up of a French National Cohort of Patients With Cutaneous Squamous Cell Carcinoma Requiring Systemic Treatment.

NCT07606508 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-07-09
Last updated
2026-05-26

Condition(s) studied

Cutaneous Squamous Cell Carcinoma (CSCC)

Investigational drug(s) / intervention(s)

Systemic treatment

Systemic treatment: Adjuvant Treatment Neoadjuvant Treatment Curative Treatment

Study summary

In the context where advanced cutaneous squamous cell carcinoma (cSCC) is currently a public health issue due to its increasing incidence and where its management is rapidly evolving, it is essential to characterize and monitor changes in therapeutic strategies for patients requiring systemic treatment with adjuvant/neoadjuvant or curative setting.

The overall objective of this study is to describe the long-term, real-life management of patients with cSCC requiring systemic therapy, including their clinical characteristics as well as treatment effectiveness and safety. To achieve this aim, the project is based on the establishment of a French national database of patients with cSCC receiving systemic therapy. This is a non-interventional multicenter study involving approximately 30 centers from the French Cutaneous Oncology Group (GCC), including a retrospective phase (from January 2020 for initiation of first-line systemic therapy) followed by a prospective phase.

Time perspective is Retrospective and Prospective

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with a diagnosis of primary cutaneous squamous cell carcinoma initiating first-line systemic therapy, whether administered with curative, adjuvant, or neoadjuvant intent. * Male or female patients. * Age ≥18 years. * No documented objection to participation in the study. Exclusion Criteria: * Patients who refuse to participate in the study or who object to the collection or processing of their personal data. * Initiation of systemic therapy prior to 2020. * Patients not requiring systemic therapy. * More than one line of systemic therapy at the time of inclusion. * Patients under legal guardianship or curatorship. * Individuals deprived of liberty. * lack of health insurance coverage.

Primary outcome measure(s)

  • Frequency and duration of treatments according to the line therapy and treatment intent (curative, adjuvant, or neoadjuvant), and their evolution over time. — Long term follow-up, Average of 5 years, Duration of the project not defined

Trial sites (29)

FacilityCityRegionStatus
CHU Dijon Bourgogne Amiens France Not Yet Recruiting
Centre Hospitalier Régional d'Orléans Annecy France Recruiting
CHRU Besançon Besançon France Recruiting
Centre Hospitalier de Blois Blois France Recruiting
Hôpital Avicenne Bobigny France Recruiting
Hôpital Saint André, Bordeaux France Recruiting
Hôpital Ambroise Paré Boulogne-Billancourt France Recruiting
CHU de Caen Caen France Not Yet Recruiting
CHRU de Tours Chambray-lès-Tours France Recruiting
CHU Estaing Clermont-Ferrand France Recruiting
CHU Henri Mondor Créteil France Recruiting
CHU Dijon Bourgogne Dijon France Recruiting
Centre Hospitalier Le Mans Le Mans France Recruiting
CHU Lille Lille France Recruiting
CHU Dijon Bourgogne Lyon France Recruiting
Hôpital de la Timone Marseille France Recruiting
CHRU Montpellier Hôpital Saint Eloi Montpellier France Recruiting
Hôpital St Eloi Montpellier France Not Yet Recruiting
CHU Nantes Nantes France Recruiting
CHU de Nice Nice France Recruiting
Centre Hospitalier Régional d'Orléans Orléans France Recruiting
Hôpital Bichat-Claude-Bernard Paris France Recruiting
Hôpital Cochin-Port Royal Paris France Not Yet Recruiting
Hôpital St Louis Paris France Recruiting
CHU Charles Nicolle Rouen France Recruiting
Institut de Cancérologie de l'Ouest Saint-Herblain France Recruiting
HIA Sainte Anne Toulon France Enrolling By Invitation
Centre Hospitalier de Valence Valence France Recruiting
CHRU de Nancy Vandœuvre-lès-Nancy France Recruiting
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 NCT07606508 on ClinicalTrials.gov ↗ ← All trials in France