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Completed

NCT Number: NCT05063058

Biomarker-driven Therapy for Melanoma

Patients included will undergo biopsy and the molecular analysis will be discussed at the institutional molecular tumor board. The recommandation of the molecular tumor board will be provided to the physician in charge of the patient for final treatment desicion.

The main endpoints are the number of patients with actionable molecular alterations, the number of patients with a treatment recommendation, the number of patients receiving the recommended therapy, overall survival of the patients treated according to recommendations or not. For patients treated according to the recommendations: Response rate and progression free survival at 6 months according to RECIST criteria.

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Key information

About this study

Eligible patients have to have a histologically proven metastatic melanoma failing standard treatments. Other inclusion criteria included age ≥ 18 years; Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2; life expectancy ≥ 24weeks; adequate renal, liver, and bone marrow functions. Previous therapy with intravenous chemotherapy, immunotherapy or major surgery at least 4 weeks before inclusion was allowed. Patients were excluded if they had a history of cardiac disease or metastatic brain or meningeal tumors. The study is approved by the institutional research ethics board.

Molecular analysis is performed at the Max Planck Institute for Molecular Genetics Berlin and a comprehensive report is made available with 4-8 weeks. The molecular tumor board interprets the data and transforms them into treatment recommendations by identifying and prioritizing predictive biomarkers. The recommendations rely on the definition of evidence levels attributed to every single aberration and the interdisciplinary discussion of the aberrations with regard to patient situation, availability of drugs, and clinical trials. The recommendations are transmitted to the physician in charge of the patient for the final decision to treat or not the patient accordingly.

The main endpoints are the number of patients with actionable molecular alterations, the number of patients with a treatment recommendation, the number of patients receiving the recommended therapy, overall survival of patients treated according to recommendations or not.

For patients treated according to the recommendations: Response rate and progression free survival at 6 months according to RECIST criteria.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • histologically proven metastatic melanoma failing standard treatments
  • age ≥ 18 years
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2
  • life expectancy ≥ 24 weeks
  • adequate renal, liver, and bone marrow functions

Exclusion criteria

  • history of cardiac disease or metastatic brain or meningeal tumors

Treatment and study plan

Molecular guided therapy

Drug

Biomarker-driven therapy according to recommandations of the precision oncology tumor board including MEK Inhibitors (Trametinib 2 mg/d, Selumetinib 75 mg 2/d), MET Inhibitors (Crizotinib 250 mg 2/d, or Cabozantinib 60mg/d), RAS Inhibitor (Sorafenib 400 mg 2/d), Cell cycle Inhibitor (Palbociclib 125 mg/d) and Checkpoint Inhibitor (Nivolumab 240 mg every 2 weeks).

Primary outcomes

  1. Feasibility (actionable molecular alterations)

    Time frame: Through study completion over 5 years

    number of patients with actionable molecular alterations

  2. Feasibility (number of patients with a treatment recommendation)

    Time frame: Through study completion over 5 years

    number of patients with a treatment recommendation

  3. Feasibility (number of patients receiving the recommended therapy)

    Time frame: Through study completion over 5 years

    number of patients receiving the recommended therapy

Secondary outcomes

  1. Overall survival

    Time frame: 5 years

    Overall survival

  2. Response rate

    Time frame: 1 year

    Response rate of the patients treated according to the recommendations

  3. Progression free survival at 6 months according to RECIST criteria

    Time frame: up to 6 months

    PFS according to RECIST criteria for the patients treated according to the recommendations

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Collaborators

  • Alacris
  • Max-Planck Institut

Registry information

Official study title

Feasibility Study of Biomarker-driven Therapy Based on a Comprehensive Molecular Analysis of Tumor Tissue and Blood Collections in Melanoma

Acronym: TREAT20plus

Important dates

Study start
2016
Primary completion
2019
Study completion
2021
First posted
Sep 30, 2021
Registry last updated
Sep 30, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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