Skin cancer, notably melanoma, poses a significant global health burden, with rising incidence and mortality rates. While
therapeutic advancements have improved outcomes, metastatic melanoma remains challenging to treat. This study aims to
systematically review systemic treatment options for advanced melanoma, focusing on efficacy and safety in the first-line
setting. Through a comprehensive search and meta-analysis of randomized controlled trials conducted from 2013 to 2023,
11 studies encompassing 2816 participants were analyzed. Treatment options included BRAF inhibitors (vemurafenib,
dabrafenib), MEK inhibitors (trametinib, cobimetinib), and immune checkpoint inhibitors (ipilimumab). Combined therapy with vemurafenib, cobimetinib, and ipilimumab demonstrated superior overall survival (OS) and progression-free
survival (PFS) compared to monotherapy, with a significant odds ratio (OR) of 6.95 (95% CI: 4.25–9.64, p0.00001)
for OS and 2.49 (95% CI: 1.42–3.56, p0.00001) for PFS. Additionally, dabrafenib and trametinib combination therapy
showed improved outcomes with favorable tolerability, including a significant reduction in adverse event (AE) risk, with
an OR of 2.20 (95% CI: 1.72–2.81). Furthermore, our analysis highlighted vemurafenib-associated dermatological toxicities, emphasizing the need for effective management strategies. The study underscores the evolving treatment landscape in
melanoma management, with a potential shift towards immune checkpoint inhibitors in the adjuvant setting, particularly
for BRAF-mutated disease. However, limitations in meta-analysis methodologies and the need for long-term investigations
into treatment implications on survival and quality of life underscore the importance of continued research.
Authors
• Anan S. Jarab
Walid A. Al-Qerem
Lina M. Khdour
Yousef A. Mimi
Maher R. Khdour
Pages From
735
Pages To
735
ISSN
03403696
Journal Name
Archives of Dermatological Research
Volume
316
Issue
10
Keywords
Melanoma · Chemotherapy · Immunotherapy · Immune checkpoint inhibitor · Cytokines
Project
Pharmacetical
Abstract