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Updated: Oct 31, 2025

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
Published on: June 7, 2019
First line treatment of BRAF mutated advanced melanoma: Does one size fit all?
Federica Giugliano1, Edoardo Crimini1, Paolo Tarantino1
1European Institute of Oncology, IRCCS, 20141 Milan, Italy; Department of Oncology and Hematology (DIPO), University of Milan, 20122 Milan, Italy.
Abstract:
In the last decade, immunotherapy and target therapy have revolutionized the prognosis of patients with BRAF-V600 mutation-positive metastatic melanoma. To date, three different combinations of BRAF/MEK inhibitors have been approved for this population, showing comparable efficacy and unique toxicity profiles. Several immune-checkpoint inhibitors, including pembrolizumab, nivolumab and the combination of nivolumab plus ipilimumab, are also available options for untreated metastatic melanoma patients. A novel approach has emerged by combining immune-checkpoint inhibitors and targeted agents, based on preclinical hints of synergy, prompting clinical results from large randomized trials. Specifically, the triplet of atezolizumab, vemurafenib and cobimetinib has been recently approved by FDA for patients with untreated BRAF-mutant metastatic melanoma. With a wide variety of available treatment options in this setting, it is paramount to establish criteria to select the most effective and safe frontline tailored approaches, for each patient. Results from ongoing studies are awaited, to maximise the benefits in survival outcomes and quality of life for patients, balancing adverse events and clinical benefit. The purpose of this review is to summarize the current landscape of standard and experimental treatment strategies for the first line treatment of patients with BRAF-mutated advanced melanoma and discuss the best patient-centered tailored strategies in the first-line setting.
Insights
Advanced melanoma treatment has evolved with immunotherapy and targeted therapies. Combining these approaches, like the BRAF/MEK inhibitor triplet, offers new options for BRAF-mutant metastatic melanoma patients.
Area of Science:
- Oncology
- Medical Science
Background:
- Immunotherapy and targeted therapy have transformed metastatic melanoma treatment.
- BRAF/MEK inhibitors and immune-checkpoint inhibitors are established options.
- Combination therapies show promise for BRAF-V600 mutation-positive melanoma.
Purpose of the Study:
- To review current first-line treatment strategies for BRAF-mutated advanced melanoma.
- To discuss patient-centered tailored approaches.
- To summarize standard and experimental therapies.
Main Methods:
- Review of recent clinical trials and FDA-approved treatments.
- Analysis of efficacy, toxicity, and combination strategies.
- Discussion of patient selection criteria for frontline therapy.
Main Results:
- Multiple BRAF/MEK inhibitor combinations and immune-checkpoint inhibitors are available.
- Atezolizumab, vemurafenib, and cobimetinib triplet is FDA-approved for untreated patients.
- Combining targeted agents and immunotherapy demonstrates synergistic potential.
Conclusions:
- Selecting optimal frontline therapy for BRAF-mutated melanoma requires careful consideration of efficacy, toxicity, and patient-specific factors.
- Ongoing research aims to maximize survival benefits and quality of life.
- Tailored treatment strategies are crucial for improving outcomes in advanced melanoma.
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