Epidemiological description of genetic alterations and prognosis in Mexican patients with melanoma: a retrospective cohort
NGS is a useful tool that can detect multiple mutations in the same patient. Detecting profiles with prognostic values and mutations for targeted therapy is an option for these patients, however, the usefulness of these results must be further studied in larger cohorts.
Authors
- Rodrigo R. Flores-Mariñelarena
- Iván Romarico González-Espinoza
- Mariana Chiquillo-Domínguez
- Julio César Garibay-Díaz
- Abraham Castro-Ponce
- Héctor Martínez‐Said (ORCID: https://orcid.org/0000-0002-9881-4592)
- Gabriela Juárez-Salazar
- Jerónimo Rafael Rodríguez‐Cid (ORCID: https://orcid.org/0000-0001-8518-9065)
- Katia Fabiola Ávila-Fernández (ORCID: https://orcid.org/0000-0002-4959-9128)
Institutions
- Hospital Médica Sur (MX)
- Universidad de Puebla (MX)
- Instituto Universitario Puebla (MX)
- Hospital Juárez de México (MX)
- Instituto Nacional de Cancerología (MX)
Publication Details
- Journal
- Cancer Treatment and Research Communications
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1016/j.ctarc.2025.100973
- Primary Topic
- Melanoma and MAPK Pathways
- Type
- article
- Field-Weighted Citation Impact
- 0.00