SEOM clinical guideline on hereditary colorectal cancer (2019)

被引：11

作者：

Guillen-Ponce, C. ^{[1
]}

Lastra, E. ^{[2
]}

Lorenzo-Lorenzo, I ^{[3
]}

Martin Gomez, T. ^{[4
]}

Morales Chamorro, R. ^{[5
]}

Sanchez-Heras, A. B. ^{[6
]}

Serrano, R. ^{[7
]}

Soriano Rodriguez, M. C. ^{[8
]}

Soto, J. L. ^{[9
]}

Robles, L. ^{[10
]}

机构：

[1] Hosp Univ Ramon y Cajal, Med Oncol Dept, IRYCIS, Carretera Colmenar Viejo,Km 9,100, Madrid 28034, Spain

[2] Hosp Univ Burgos, Med Oncol Dept, Burgos, Spain

[3] Complejo Hosp Univ Vigo CHUVI, Med Oncol Dept, Pontevedra, Spain

[4] Hosp Univ Salamanca, Med Oncol Dept, Salamanca, Spain

[5] Hosp Gen La Mancha Ctr, Med Oncol Dept, Ciudad Real, Spain

[6] Hosp Gen Univ Elche, Med Oncol Dept, Alicante, Spain

[7] Hosp Univ Reina Sofia, Med Oncol Dept, CIBERONC, IMIBIC, Cordoba, Spain

[8] Hosp Gen Virgen de la Luz, Med Oncol Dept, Cuenca, Spain

[9] Hosp Gen Univ Elche, Mol Genet Lab, Alicante, Spain

[10] Hosp Univ Doce Octubre, Med Oncol Dept, Madrid, Spain

来源：

CLINICAL & TRANSLATIONAL ONCOLOGY | 2020年 / 22卷 / 02期

关键词：

Lynch syndrome; Adenomatous polyposis; Hereditary colorectal cancer; Colon cancer; MISMATCH-REPAIR DEFICIENCY; SUSCEPTIBILITY GENE-MUTATIONS; LYNCH SYNDROME; ENDOMETRIAL CANCERS; COST-EFFECTIVENESS; GERMLINE; RISK; COLON; MANAGEMENT; GRADE;

D O I：

10.1007/s12094-019-02272-y

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

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.

引用

页码：201 / 212

页数：12

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