SEOM clinical guideline on hereditary colorectal cancer (2019)


Por: Guillen-Ponce, C, Lastra, E, Lorenzo-Lorenzo, I, Gomez, T, Chamorro, R, Sanchez-Heras, A, Serrano, R, Rodriguez, M, Soto J and Robles, L

Publicada: 1 feb 2020 Ahead of Print: 1 ene 2020
Resumen:
In the last 2 decades, clinical genetics on hereditary colorectal syndromes has shifted from just a molecular characterization of the different syndromes to the estimation of the individual risk of cancer and appropriate risk reduction strategies. In the last years, new specific therapies for some subgroups of patients have emerged as very effective alternatives. At the same time, germline multigene panel testing by next-generation sequencing (NGS) technology has become the new gold standard for molecular genetics.

Filiaciones:
Guillen-Ponce, C:
 Hosp Univ Ramon y Cajal, Med Oncol Dept, IRYCIS, Carretera Colmenar Viejo,Km 9,100, Madrid 28034, Spain

Lastra, E:
 Hosp Univ Burgos, Med Oncol Dept, Burgos, Spain

Lorenzo-Lorenzo, I:
 Complejo Hosp Univ Vigo CHUVI, Med Oncol Dept, Pontevedra, Spain

Gomez, T:
 Hosp Univ Salamanca, Med Oncol Dept, Salamanca, Spain

Chamorro, R:
 Hosp Gen La Mancha Ctr, Med Oncol Dept, Ciudad Real, Spain

:
 Hosp Gen Univ Elche, Med Oncol Dept, Alicante, Spain

Serrano, R:
 Hosp Univ Reina Sofia, Med Oncol Dept, CIBERONC, IMIBIC, Cordoba, Spain

Rodriguez, M:
 Hosp Gen Virgen de la Luz, Med Oncol Dept, Cuenca, Spain

Soto J:
 Hosp Gen Univ Elche, Mol Genet Lab, Alicante, Spain

Robles, L:
 Hosp Univ Doce Octubre, Med Oncol Dept, Madrid, Spain
ISSN: 1699048X





CLINICAL & TRANSLATIONAL ONCOLOGY
Editorial
SPRINGER-VERLAG ITALIA SRL, VIA DECEMBRIO, 28, MILAN, 20137, ITALY, Italia
Tipo de documento: Article
Volumen: 22 Número: 2
Páginas: 201-212
WOS Id: 000509156800003
ID de PubMed: 31981079
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