Multicenter Tissue Registry in Melanoma

Study Purpose

The prospective multicenter translational study Tissue Registry in Melanoma (ADOREG/TRIM; CA209-578) aimed to validate the Tumor Mutational Burden (TMB) and the PD-L1 expression (PD-L1) from a pre-therapeutically obtained tumor tissue sample as a predictor of a subsequent systemic therapy in a large real-world cohort of metastatic melanoma patients.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Observational [Patient Registry]
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Patients with histologically confirmed melanoma stage III or
  • IV. 2.
Clinically eligible for systemic cancer therapy (immune checkpoint inhibitors, targeted agents). 3. Tumor tissue biopsy already existing (metastasis tissue as recent as possible, but older tissue material or primary tumor tissue also possible). 4. Patient has given written informed consent for the current study as well as for his data to be entered into the ADOREG online database system. 5. Patient is ≥18 years old.

Exclusion Criteria:

-

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT05750511
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Dermatologic Cooperative Oncology Group
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Dirk Schadendorf, MD
Principal Investigator Affiliation Dermatologic Cooperative Oncology Group
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries Germany
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Metastatic Melanoma
Additional Details

The aim of the present study is to identify and validate molecular and clinical biomarkers of therapy outcome in metastatic melanoma. Clinical and molecular parameters of melanoma patients and their tumors will be collected in an online-based registry (ADOREG), and thereafter correlated with the outcome of subsequent systemic therapies in terms of progression-free survival, overall survival, and treatment response. Systemic therapies will include all types of currently used regimens (kinase inhibitors, immune checkpoint inhibitors, chemotherapy). FFPE tissue samples will comprise different time points (primary tumors versus metastases) as well as tumor sites (lymph node versus organ metastases) to identify potential differences in the predictive value of these materials. The anticipated results from these analyses are of essential importance for future patient selection for individualized therapy strategies.

Arms & Interventions

Arms

: metastatic melanoma

1,000 subjects with metastatic melanoma stage III or IV suitable for systemic treatment from centers of the German Dermatologic Cooperative Oncology Group (DeCOG)

Interventions

Diagnostic Test: - molecular tissue analysis

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Tuebingen, Baden-Württemberg, Germany

Status

Recruiting

Address

Dept. of Dermatology, University Hospital Tuebingen

Tuebingen, Baden-Württemberg, D-72076

Site Contact

Andrea Forschner, MD

[email protected]

+49-7071-2980872

Buxtehude, Niedersachsen, Germany

Status

Recruiting

Address

Department of Dermatology, ElbeKliniken - Klinikum Buxtehude

Buxtehude, Niedersachsen, 21614

Site Contact

Peter Mohr, MD

[email protected]

+49 4161 7030

Homburg/Saar, Saarland, Germany

Status

Recruiting

Address

Department of Dermatology, The Saarland University Hospital

Homburg/Saar, Saarland, 66424

Site Contact

Claudia Pfoehler, MD

[email protected]

+49 6841 3801

Lübeck, Schleswig-Holstein, Germany

Status

Recruiting

Address

Dept. of Dermatology, University of Schleswig-Holstein, Campus Lübeck

Lübeck, Schleswig-Holstein, D-23538

Site Contact

Patrick Terheyden, MD

[email protected]

+49-451-5002517

Erfurt, Thuringia, Germany

Status

Recruiting

Address

Dept. of Dermatology, Helios Clinic Erfurt

Erfurt, Thuringia, 99012

Site Contact

Rudolf herbst, MD

[email protected]

+49-361-7814300

Augsburg, Germany

Status

Recruiting

Address

Department of Dermatology, University Hospital

Augsburg, ,

Site Contact

Julia Welzel

[email protected]

+49 201 723 85364

Dresden, Germany

Status

Recruiting

Address

Department of Dermatology, University Hospital

Dresden, ,

Site Contact

Friedegund Meier

[email protected]

+49 201 723 85364

Essen, Germany

Status

Recruiting

Address

Department of dermatology, University Hospital

Essen, ,

Site Contact

Selma Ugurel

[email protected]

+49 201 723 85364

Hannover, Germany

Status

Recruiting

Address

Medizinische Hochschule,dermatologische Klinik und Poliklinik

Hannover, , 30449

Site Contact

Inke Grimmelmann, MD

[email protected]

0049(0)511 92 460

Department of Dermatology, Ludwigshafen, Germany

Status

Recruiting

Address

Department of Dermatology

Ludwigshafen, ,

Site Contact

Edgar Dippel

[email protected]

+49 201 723 85364

Skin Cancer Unit, University Hospital, Mannheim, Germany

Status

Recruiting

Address

Skin Cancer Unit, University Hospital

Mannheim, ,

Site Contact

Jochen Utikal

[email protected]

+49 201 723 85364

Minden, Germany

Status

Recruiting

Address

Department of Dermatology, University Hospital

Minden, ,

Site Contact

Ralf Gutzmer

[email protected]

+49 201 723 85364

Department of Dermatology, Oberhausen, Germany

Status

Recruiting

Address

Department of Dermatology

Oberhausen, ,

Site Contact

Alexander Kreuter

[email protected]

+49 201 723 85364

Department of Dermatology, Quedlinburg, Germany

Status

Recruiting

Address

Department of Dermatology

Quedlinburg, ,

Site Contact

Jens Ulrich

[email protected]

+49 201 723 85364

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