Description of the SAGhE Cohort: A Large European Study of Mortality and Cancer Incidence Risks after Childhood Treatment with Recombinant Growth Hormone

Horm Res Paediatr. 2015;84(3):172-83. doi: 10.1159/000435856. Epub 2015 Jul 23.

Abstract

Background: The long-term safety of growth hormone treatment is uncertain. Raised risks of death and certain cancers have been reported inconsistently, based on limited data or short-term follow-up by pharmaceutical companies.

Patients and methods: The SAGhE (Safety and Appropriateness of Growth Hormone Treatments in Europe) study assembled cohorts of patients treated in childhood with recombinant human growth hormone (r-hGH) in 8 European countries since the first use of this treatment in 1984 and followed them for cause-specific mortality and cancer incidence. Expected rates were obtained from national and local general population data. The cohort consisted of 24,232 patients, most commonly treated for isolated growth failure (53%), Turner syndrome (13%) and growth hormone deficiency linked to neoplasia (12%). This paper describes in detail the study design, methods and data collection and discusses the strengths, biases and weaknesses consequent on this.

Conclusion: The SAGhE cohort is the largest and longest follow-up cohort study of growth hormone-treated patients with follow-up and analysis independent of industry. It forms a major resource for investigating cancer and mortality risks in r-hGH patients. The interpretation of SAGhE results, however, will need to take account of the methods of cohort assembly and follow-up in each country.

MeSH terms

  • Adolescent
  • Cause of Death
  • Child
  • Child, Preschool
  • Cohort Studies
  • Europe / epidemiology
  • Female
  • Follow-Up Studies
  • Growth Disorders / drug therapy
  • Human Growth Hormone / adverse effects*
  • Human Growth Hormone / therapeutic use
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Male
  • Neoplasms / epidemiology*
  • Neoplasms / mortality*
  • Recombinant Proteins / adverse effects
  • Recombinant Proteins / therapeutic use
  • Risk
  • Young Adult

Substances

  • Recombinant Proteins
  • Human Growth Hormone