Neoadjuvant Immunotherapy of Operable Metastatic Melanoma in Real Life (GCC)

Last updated: September 6, 2024
Sponsor: Centre Hospitalier Universitaire de Besancon
Overall Status: Active - Recruiting

Phase

N/A

Condition

Melanoma

Treatment

N/A

Clinical Study ID

NCT06586593
2023/758
  • Ages > 18
  • All Genders

Study Summary

This study aims to evaluate efficacy and tolerance of real life neoadjuvant immunotherapy in advanced yet operable melanoma.

The complete histological response will be assessed.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with operable metastatic melanoma (stage III or IV of American JointCommittee on Cancer [AJCC] Stages CLassification) treated with neoadjuvantimmunotherapy (anti-PD1 or anti-PD1 + anti-CTLA-4), even if surgery cancelled due todisease progression or complete response or patient's refusal to be operated.

  • Efficacy of the neoadjuvant immunotherapy histologically of radiologically assessed

Exclusion

Exclusion Criteria:

  • Uveal melanoma

Study Design

Total Participants: 77
Study Start date:
March 24, 2023
Estimated Completion Date:
January 31, 2025

Connect with a study center

  • CHU Angers

    Angers,
    France

    Site Not Available

  • CHU de Besançon

    Besançon,
    France

    Active - Recruiting

  • Hôpital Avicenne

    Bobigny,
    France

    Site Not Available

  • CH de Boulogne-sur-Mer

    Boulogne-sur-Mer,
    France

    Site Not Available

  • CHU Clermont-Ferrand

    Clermont-Ferrand,
    France

    Site Not Available

  • Centre de Lutte Contre le Cancer Léon Bérard

    Lyon,
    France

    Site Not Available

  • ICO René Gauducheau

    Saint-Herblain,
    France

    Site Not Available

  • Institut Universitaire de Cancérologie de Toulouse

    Toulouse,
    France

    Site Not Available

  • CH de Valence

    Valence,
    France

    Site Not Available

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