A comparative study of the cutaneous side effects between BRAF monotherapy and BRAF/MEK inhibitor combination therapy in patients with advanced melanoma: a single-centre experience
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Updated: Feb 19, 2026

A Melanoma Patient-Derived Xenograft Model
Published on: May 20, 2019
Irene Russo1, Ludovica Zorzetto1, Anna Chiara Frigo2
1Unit of Dermatology, University of Padua, Via Gallucci 4, 35128 Padova, Italy.
Abstract:
Patients with advanced melanoma have a poor prognosis. Since the discovery of BRAF mutations in cutaneous melanoma, new pharmacological agents have been developed to inhibit this target. Although the survival of patients with advanced melanoma has improved with BRAF inhibitors, the emergence of drug resistance and the high incidence of cutaneous side effects represent important limitations. The aim of our study was to compare the incidence of cutaneous side effects between BRAF inhibitor monotherapy and BRAF and MEK inhibitor combination therapy in our cohort of patients. This study was a longitudinal prospective observational study. The study population comprised 83 patients with advanced cutaneous melanoma presenting with BRAF V600 mutation. The inclusion criteria included: age above 18 years, metastatic cutaneous melanoma or melanoma with high risk of metastasis, the presence of BRAF V600 mutation, and treatment with BRAF inhibitors or a combination of BRAF and MEK inhibitors. The majority of patients developed skin toxicity during treatment. The most common cutaneous side effects were localized hyperkeratosis and verrucous keratosis. Other cutaneous side effects observed were photosensitivity, squamous cell carcinoma, and keratoacanthoma. Our results indicate that cutaneous side effects are generally observed during BRAF inhibitor monotherapy and are significantly different from those observed in patients treated with combination therapy.
Insights
BRAF inhibitors improve advanced melanoma survival but cause skin side effects. Combination therapy shows different cutaneous toxicity compared to BRAF inhibitor monotherapy.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Advanced melanoma historically has a poor prognosis.
- BRAF mutations are key targets for new melanoma therapies.
- BRAF inhibitors improve survival but present limitations like drug resistance and skin toxicity.
Purpose of the Study:
- To compare the incidence and types of cutaneous side effects between BRAF inhibitor monotherapy and BRAF/MEK inhibitor combination therapy.
- To analyze skin toxicity profiles in patients with BRAF V600-mutated advanced cutaneous melanoma.
Main Methods:
- Longitudinal prospective observational study.
- Inclusion of 83 patients with advanced cutaneous melanoma and BRAF V600 mutation.
- Treatment groups: BRAF inhibitor monotherapy vs. BRAF and MEK inhibitor combination therapy.
Main Results:
- Most patients experienced skin toxicity during treatment.
- Common side effects included localized hyperkeratosis and verrucous keratosis.
- Other toxicities: photosensitivity, squamous cell carcinoma, and keratoacanthoma.
- Cutaneous side effects differed significantly between monotherapy and combination therapy groups.
Conclusions:
- Cutaneous side effects are common in advanced melanoma patients treated with BRAF inhibitors.
- The pattern of skin toxicity varies between BRAF inhibitor monotherapy and combination therapy.
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