SEOM clinical guidelines for hereditary cancer

  • Begoña Graña
  • Enrique Lastra
  • Gemma Llort
  • Joan Brunet
  • Dolores Isla
Clinical Guides in Oncology

DOI: 10.1007/s12094-011-0701-2

Cite this article as:
Graña, B., Lastra, E., Llort, G. et al. Clin Transl Oncol (2011) 13: 580. doi:10.1007/s12094-011-0701-2


Research in genetics has facilitated the identification of highly penetrant genes responsible for a large number of diseases. In the oncology field, genetic counselling and gene testing are focused on the two most common syndromes in familial cancer: hereditary breast and ovarian cancer syndrome (HBOC) and hereditary non-polyposis colorectal cancer or Lynch syndrome (LS). The objective of this guideline in hereditary cancer is to summarise the current state of knowledge and make recommendations in the areas of diagnosis, prevention and treatment of hereditary cancer.


Hereditary cancerBRCA1BRCA2Lynch syndrome

Copyright information

© Feseo 2011

Authors and Affiliations

  • Begoña Graña
    • 1
    • 2
  • Enrique Lastra
    • 3
  • Gemma Llort
    • 4
  • Joan Brunet
    • 5
  • Dolores Isla
    • 6
  1. 1.High Risk and Cancer Prevention Unit Medical Oncology DepartmentVall d’Hebron Institute of Oncology (VHIO)BarcelonaSpain
  2. 2.Marcide HospitalFerrol Healthcare AreaA CoruñaSpain
  3. 3.Genetic Counselling Unit Medical Oncology SectionGeneral Yagüe HospitalBurgosSpain
  4. 4.Genetic Counselling UnitValles Institute of OncologySabadell-Terrassa, BarcelonaSpain
  5. 5.Medical Oncology Department Hereditary Cancer ProgramCatalan Institut of Oncology (ICO)GironaSpain
  6. 6.Medical Oncology DepartmentLozano Blesa HospitalZaragozaSpain