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Detalle de: Prevalence of pathogenic germline variants in patients with metastatic renal cell carcinoma

Title Prevalence of pathogenic germline variants in patients with metastatic renal cell carcinoma
Abstract

Purpose Germline pathogenic variants are estimated to affect 3-5% of renal cell carcinoma (RCC) patients. However, higher mutational prevalence in non-clear cell RCC (non-ccRCC) and advanced disease has been suggested. Methods To clarify the prevalence of pathogenic germline variants in metastatic RCC, we sequenced 29 cancer susceptibility genes in 294 unselected metastatic RCC cases plus 21 patients with clinical hereditary features. In 145 tumors, genes frequently mutated in RCC were sequenced and methylation was assessed in selected cases. Results Germline variants in RCC predisposition genes (FH, VHL) were detected in 1.4% of the unselected metastatic patients, with higher frequency in non-ccRCC versus ccRCC (6.4% and 0.4%; P = 0.0025) and in younger patients (P = 0.036). Among the 315 studied patients, 14% of non-type 1 papillary cases (4 of 28), all metastatic Conclusion Our findings confirm a high prevalence of pathogenic germline variants in RCC predisposition genes in metastatic non-ccRCC, and highlight that metastatic patients with papillary type 2 or unconventional histologies compatible with FH would benefit from genetic screening.

Apa Reference Santos, M., Lanillos, J., Roldan-Romero, J.M., Caleiras, E., Montero-Conde, C., Cascón, A., Climent, M.A., Anguera, G., Hernando, S., Laínez, N., Robledo, M., Robles, L., de Velasco, G., García-Donas, J. & Rodriguez-Antona, C. (2021). Prevalence of pathogenic germline variants in patients with metastatic renal cell carcinoma. Genetics in Medicine, 23(4), 698-704. 10.1038/s41436-020-01062-0
Doi 10.1038/s41436-020-01062-0
Publication Date Apr 2021
Publication Type Article
Researcher María Santos Romero
Ontology Mutation Analysis and design
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