SEOM clinical guidelines for hereditary cancer

Clin Transl Oncol. 2011 Aug;13(8):580-6. doi: 10.1007/s12094-011-0701-2.

Abstract

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.

Publication types

  • Practice Guideline

MeSH terms

  • Adult
  • Biomarkers, Tumor
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / genetics
  • Breast Neoplasms / therapy
  • Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics
  • Colorectal Neoplasms, Hereditary Nonpolyposis / therapy
  • Female
  • Genes, BRCA1
  • Genes, BRCA2
  • Humans
  • Male
  • Medical Oncology / methods*
  • Middle Aged
  • Neoplasm Staging / methods
  • Neoplasms / diagnosis
  • Neoplasms / genetics*
  • Neoplasms / therapy*
  • Ovarian Neoplasms / diagnosis
  • Ovarian Neoplasms / genetics
  • Ovarian Neoplasms / therapy
  • Societies, Medical
  • Treatment Outcome

Substances

  • Biomarkers, Tumor