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Search / Trial NCT02828202

Follow-up of a National Cohort of Melanoma Resectable Stage II, Stage III or IV Patients or Unresectable Primary

Launched by ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS · Jul 6, 2016

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Melanoma Skin Biobank

ClinConnect Summary

This clinical trial, called MELBASE, is focused on studying advanced melanoma, which is a serious type of skin cancer. The goal is to gather important information about patients with different stages of melanoma, particularly those who can have their tumors surgically removed (resectable stage II or III) and those with more advanced or inoperable melanoma (unresectable stage III or IV). By collecting data over 10 years, researchers hope to learn more about the disease, including new ways to predict how patients will respond to treatments, the overall quality of life for patients, and the costs associated with their care.

To join the trial, patients must be at least 18 years old and have a confirmed diagnosis of melanoma that fits specific criteria. For instance, those with resectable stage II or III melanoma who haven’t received prior systemic treatments are eligible, as well as those with advanced, unresectable melanoma. Participants can expect regular evaluations and monitoring throughout the study, contributing to a better understanding of melanoma and potentially helping to improve future treatments. It's important to note that patients who have other specific conditions or types of melanoma may not qualify for this trial.

Gender

ALL

Eligibility criteria

  • 1. Cohort Patients with Resectable stage II or III
  • Inclusion Criteria:
  • Patients diagnosed with resectable stage IIA/IIB/IIC or III melanoma, confirmed by histological exam.
  • Naïve of systemic treatment for resectable stage II or III. Whose metastatic tumoral material can be collected by the Biological Resource Centers (optional criteria).
  • Aged ≥ 18 years. Consenting to participate (signed informed consent).
  • Exclusion Criteria:
  • Patients refusal. Choroid melanoma. Resectable stage 1 melanoma. Stage 4, unresectable primitive or unresectable stage 3 melanoma. Patients under guardianship and under trusteeship.
  • 2. Cohort patients with Unresectable stage III or stage IV (resectable or not) or unresectable primary:
  • Inclusion Criteria:
  • Patients diagnosed with an advanced melanoma, confirmed by histological exam. Unresectable primitive or unresectable stage III or stage IV (resectable or not) melanoma ; or patients treated by neoadjuvant treatment (exceptional) Naïve of systemic treatment for unresectable primitive or unresectable stage III or stage IV (resectable or not) melanoma, except adjuvant treatment.
  • Whose metastatic tumoral material can be collected by the Biological Resource Centers (optional criteria).
  • Aged ≥ 18 years. Consenting to participate (signed informed consent).
  • Exclusion Criteria:
  • Resectable stage 1, 2 or 3 melanoma. Patients refusal. Choroid melanoma. Patients under guardianship and under trusteeship.

About Assistance Publique Hôpitaux De Paris

Assistance Publique - Hôpitaux de Paris (AP-HP) is a leading public hospital system in France, renowned for its commitment to healthcare excellence and innovative medical research. As a prominent clinical trial sponsor, AP-HP plays a pivotal role in advancing medical knowledge and improving patient care through rigorous scientific investigations across a wide range of therapeutic areas. With a focus on collaboration and interdisciplinary approaches, AP-HP leverages its extensive network of hospitals and expert clinicians to facilitate high-quality clinical trials that adhere to the highest ethical and regulatory standards, ultimately aiming to translate research findings into tangible health benefits for diverse patient populations.

Locations

Villejuif, , France

Grenoble, , France

Nantes, , France

Lille, , France

Caen, , France

Toulouse, , France

Nice, , France

Lyon, , France

Rennes, , France

Amiens, , France

Brest, , France

Nancy, , France

Nice, , France

Montpellier, , France

Toulouse, , France

Annecy, , France

Nîmes, , France

Besançon, , France

Dijon, , France

Lyon, , France

Bobigny, , France

Bordeaux, , France

Bordeaux, , France

Boulogne Billancourt, , France

Marseille, , France

Paris, , France

Paris, , France

Paris, , France

Rennes, , France

Créteil, , France

Patients applied

0 patients applied

Trial Officials

Celeste Lebbe, MD, PhD

Study Director

AP-HP, Hopital Saint-Louis, centre d'oncodermatologie, Paris

Gaelle Quereux, MD, PhD

Study Director

Nantes University Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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