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Updated: May 4, 2026

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
Treatment algorithms in stage IV melanoma
Enrique Espinosa1, Jean-Jacques Grob, Reinhard Dummer
11Service of Oncology, Hospital La Paz, Madrid, Spain; 2Department of Dermatology, Hopital Ste Marguerite, Marseille, France; 3Department of Dermatology, University Hospital of Zurich, Zurich, Switzerland; 4Department of Sarcoma and Melanoma, M. Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland; 5Department of Dermatology (CR), and General Director (AE), Institute Gustave Roussy, Villejuif Cedex, France; 6First Department of Medicine, University of Athens Medical School, Athens, Greece; 7Department of Oncology, Westmead Hospital and Melanoma Institute Australia, University of Sydney, Sydney, Australia; 8Service of Oncology, Clinica Universitaria de Navarra, Pamplona, Spain; 9Department of Dermatology, University of Kiel, Kiel, Germany; and 10Department of Dermatology, University Hospital Essen, Essen, Germany.
Molecular tumor genotyping guides advanced melanoma treatment. Targeted therapies like BRAF and KIT inhibitors, alongside immunotherapy and chemotherapy, offer personalized options for stage IV melanoma patients, improving survival outcomes.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Advanced melanoma treatment is evolving with molecular classification and new targeted therapies.
- Personalized medicine approaches are crucial for improving patient outcomes in stage IV melanoma.
Purpose of the Study:
- To develop a therapeutic algorithm for stage IV melanoma based on molecular profiling.
- To guide treatment selection for advanced melanoma patients using tumor genotyping.
Main Methods:
- Review of recent key studies on advanced melanoma therapies.
- Expert forum discussion to formulate a therapeutic strategy.
- Analysis of molecular targets like BRAF and KIT mutations.
Main Results:
- BRAF inhibitors (vemurafenib, dabrafenib) are recommended for BRAF-mutated melanoma.
- KIT inhibitors show efficacy in KIT-mutant tumors, particularly with exon 11 and 13 mutations.
- Ipilimumab and chemotherapy serve as options for specific patient groups and treatment lines.
Conclusions:
- Tumor genotyping is essential for selecting appropriate therapies in advanced melanoma.
- A multi-modal therapeutic algorithm incorporating targeted agents, immunotherapy, and chemotherapy is proposed.
- Clinical trial participation is strongly encouraged for long-term survival and potential cure.
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