Frequency of BRAF V600E Mutation in the Mexican Population of Patients With Metastatic Melanoma


Por: Ruiz-Garcia, Erika, Matus-Santos, Juan A., Alberto Guadarrama-Orozco, Jorge, Angel Alvarez-Avitia, Miguel, Luis Aguilar-Ponce, Jose, Fernandez-Figueroa, Edith, Maldonado-Mendoza, Jessica, Lopez-Camarillo, Cesar, Marchat, Laurence A., Lino-Silva, Saul, Cuellar-Hubbe, Mario, de la Garza-Salazar, Jamie, Meneses-Garcia, Abelardo, Astudillo-de la Vega, Horacio, Martinez-Said, Hector

Publicada: 12 jun 2017
Categoría: Medicine (miscellaneous)

Resumen:
Purpose The BRAF V600E mutation has been described in melanomas occurring in the Caucasian, European, and Asian populations. However, in the Mexican population, the status and clinical significance of BRAF mutation has not been researched on a large scale. Methods Consecutive BRAF-tested Mexican patients with metastatic melanoma (n=127) were analyzed for mutations in exon 15 of the BRAF gene in genomic DNA by real-time polymerase chain reaction technology for amplification and detection. The results were correlated with the clinical-pathologic features and the prognosis of the patients. Results The frequency of somatic mutation V600E within the BRAF gene was 54.6% (43 of 127 patients). Nodular melanoma was the most prevalent subtype in our population, with BRAF mutations in 37.2% (16 of 55 patients). In contrast, superficial spread had a frequency of 18.6% BRAF mutation (eight of 24). Other clinicopathologic features were assessed to correlate with the mutation status. Conclusion This study searched for the most prevalent BRAF V600E mutation type in melanoma in a heterogeneous population from Mexico. Nodular melanoma was found to be the most prevalent in metastatic presentation and the presence of BRAF V600E mutation, perhaps related to the mixed ancestry; in the north, ancestry is predominantly European and in the south, it is predominantly Asian. The outcomes of the mutation correlations were similar to those found in other populations. J Glob Oncol 00. (C) 2017 by American Society of Clinical Oncology

Filiaciones:
Ruiz-Garcia, Erika:
 Natl Canc Inst, Mexico City, DF, Mexico

Matus-Santos, Juan A.:
 Natl Canc Inst, Mexico City, DF, Mexico

Alberto Guadarrama-Orozco, Jorge:
 Natl Canc Inst, Mexico City, DF, Mexico

Angel Alvarez-Avitia, Miguel:
 Natl Canc Inst, Mexico City, DF, Mexico

Luis Aguilar-Ponce, Jose:
 Natl Canc Inst, Mexico City, DF, Mexico

Fernandez-Figueroa, Edith:
 Natl Canc Inst, Mexico City, DF, Mexico

Maldonado-Mendoza, Jessica:
 Natl Canc Inst, Mexico City, DF, Mexico

Lopez-Camarillo, Cesar:
 Autonomous Univ Mexico City, Mexico City, DF, Mexico

Marchat, Laurence A.:
 Natl Polytech Inst, Mexico City, DF, Mexico

Lino-Silva, Saul:
 Natl Canc Inst, Mexico City, DF, Mexico

Cuellar-Hubbe, Mario:
 Natl Canc Inst, Mexico City, DF, Mexico

de la Garza-Salazar, Jamie:
 Natl Canc Inst, Mexico City, DF, Mexico

Meneses-Garcia, Abelardo:
 Natl Canc Inst, Mexico City, DF, Mexico

Astudillo-de la Vega, Horacio:
 Med Ctr Siglo XXI, Mexico City, DF, Mexico

Martinez-Said, Hector:
 Natl Canc Inst, Mexico City, DF, Mexico
ISSN: 23789506





Journal Of Global Oncology
Editorial
American Society of Clinical Oncology, 2318 MILL ROAD, STE 800, ALEXANDRIA, VA 22314 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 4 Número:
Páginas:
WOS Id: 000462532200001
ID de PubMed: 30241212

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