Impact of Driver Mutations on Metastasis-Free Survival in Uveal Melanoma: A Meta-Analysis

Author:

Lamas-Francis David1ORCID,Rodríguez-Fernández Carmen Antía23ORCID,de Esteban-Maciñeira Elia1ORCID,Silva-Rodríguez Paula45,Pardo María6ORCID,Bande-Rodríguez Manuel1,Blanco-Teijeiro María José1

Affiliation:

1. Department of Ophthalmology, University Hospital of Santiago de Compostela, 15706 Santiago de Compostela, Spain

2. Department of Ophthalmology, Vall d’Hebron University Hospital, 08035 Barcelona, Spain

3. FarmaChusLab Group, Health Research Institute of Santiago de Compostela (FIDIS), 15706 Santiago de Compostela, Spain

4. Fundación Pública Galega de Medicina Xenómica, 15706 Santiago de Compostela, Spain

5. Translational Ophthalmology Group, Health Research of Santiago de Compostela (IDIS), 15706 Santiago de Compostela, Spain

6. Obesidomics Group, Health Research Institute of Santiago de Compostela (IDIS), 15706 Santiago de Compostela, Spain

Abstract

The prognosis of uveal melanoma is significantly influenced by the risk of metastasis, which varies according to clinical and genetic features. Driver mutations can predict the likelihood of disease progression and survival, although the data in the literature are inconsistent. This meta-analysis aimed to evaluate the prognostic significance of driver mutations, including GNAQ, GNA11, BAP1, and SF3B1, in the advancement of uveal melanoma. A comprehensive search of databases yielded relevant studies, and data from 13 studies (848 eyes) were synthesized to assess the impact of these mutations on metastasis-free survival. The BAP1 mutation and negative immunohistochemistry were associated with a higher risk of metastasis (logHR = 1.44, 95% CI 1.05–1.83). GNAQ, GNA11, and SF3B1 mutations did not show a significant increase in risk. In summary, BAP1 has proven to reliably predict the likelihood of disease progression in uveal melanoma, while further studies are needed to establish the significance of other driver mutations.

Publisher

MDPI AG

Reference44 articles.

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