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Concurrent RAS and RAS/BRAF V600E Variants in Colorectal Cancer: More Frequent Than Expected? A Case Report.
Zelli, Veronica; Parisi, Alessandro; Patruno, Leonardo; Cannita, Katia; Ficorella, Corrado; Luzi, Carla; Compagnoni, Chiara; Zazzeroni, Francesca; Alesse, Edoardo; Tessitore, Alessandra.
Afiliación
  • Zelli V; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Parisi A; Center for Molecular Diagnostics and Advanced Therapies, University of L'Aquila, L'Aquila, Italy.
  • Patruno L; Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
  • Cannita K; Medical Oncology Unit, St. Salvatore Hospital, L'Aquila, Italy.
  • Ficorella C; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Luzi C; Medical Oncology Unit, St. Salvatore Hospital, L'Aquila, Italy.
  • Compagnoni C; Medical Oncology Unit, "Giuseppe Mazzini" Hospital, Teramo, Italy.
  • Zazzeroni F; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Alesse E; Medical Oncology Unit, St. Salvatore Hospital, L'Aquila, Italy.
  • Tessitore A; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Front Oncol ; 12: 863639, 2022.
Article en En | MEDLINE | ID: mdl-35463316
The assessment of RAS and BRAF mutational status is one of the main steps in the diagnostic and therapeutic algorithm of metastatic colorectal cancer (mCRC). Multiple mutations in the BRAF and RAS pathway are described as a rare event, with concurrent variants in KRAS and BRAF genes observed in approximately 0.05% of mCRC cases. Here, we report data from a case series affected by high-risk stage III and stage IV CRC and tested for RAS and BRAF mutation, treated at our Medical Oncology Unit. The analysis of KRAS, NRAS (codons 12, 13, 59, 61, 117, 146), and BRAF (codon 600) hotspot variants was performed in 161 CRC tumors from August 2018 to September 2021 and revealed three (1.8%) patients showing mutations in both KRAS and BRAF (V600E), including two cases with earlier CRC and one with metastatic disease. We also identified one patient (0.6%) with a mutation in both KRAS and NRAS genes and another one (0.6%) with a double KRAS mutation. Notably, the latter was characterized by aggressive behavior and poor clinical outcome. The mutational status, pathological features, and clinical history of these five CRC cases are described. Overall, this study case series adds evidence to the limited available literature concerning both the epidemiological and clinical aspects of CRC cases characterized by the presence of concurrent RAS/BRAF variants. Future multicentric studies will be required to increase the sample size and provide additional value to results observed so far in order to improve clinical management of this subgroup of CRC patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: Front Oncol Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: Front Oncol Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza