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Clinical Trials in France / NCT06809491
Active, not recruiting Observational

One-year Recurrence-free Survival of Melanoma Patients Eligible for a Sentinel Lymph Node Biopsy

NCT06809491 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-01-23
Last updated
2025-02-05

Condition(s) studied

Melanoma, SkinAdjuvant Treatment

Study summary

Melanoma is one of the most aggressive solid cancers, although mortality can be reduced with early treatment. Immunotherapy has transformed the prognosis of this pathology.

The sentinel lymph node technique is used to classify the severity of melanoma. It is proposed for melanomas with a Breslow thickness of 0.8 mm to 1 mm, and recommended for melanomas greater than 1 mm or with ulceration, whatever the Breslow index.

This technique is particularly useful for assessing pathology by detecting the presence of lymph node metastases. Patients with lymph node involvement (micro or macro) are eligible for adjuvant treatment.

The new recommendations suggest adjuvant immunotherapy for stages IIB and IIC (without lymph node involvement assessed by the sentinel lymph node technique). This procedure is widely used at the CHRU de NANCY.

The aim of this study is to demonstrate the value of the sentinel lymph node in assessing the risk of melanoma recurrence at one year (or more).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Major patient with a melanoma with a Breslow index greater than 0.8mm or ulcerated melanoma, non-metastatic at diagnosis, Exclusion Criteria: * Metastatic patient * Minor patient * Melanoma with a Breslow index of less than 0.8mm and not ulcerated * Patient objecting to data collection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHRU Nancy Vandœuvre-lès-Nancy Grand Est

More Central Hospital, Nancy, France trials in France

Other trials for the same condition

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 NCT06809491 on ClinicalTrials.gov ↗ ← All trials in France