Establishing a large prospective clinical cohort in people with head and neck cancer as a biomedical resource: head and neck 5000

Andy R Ness, Andrea E Waylen, Katrina Hurley, Mona Jeffreys, Christopher Penfold, Miranda Pring, Sam D Leary, Christine Allmark, Stu Toms, Susan M Ring, Tim J Peters, William Hollingworth, Helen Worthington, Chris Nutting, Sheila Fisher, Simon Rogers, Steve J Thomas

Research output: Contribution to journalArticle (Academic Journal)peer-review

27 Citations (Scopus)
326 Downloads (Pure)

Abstract

BACKGROUND: Head and neck cancer is an important cause of ill health. Survival appears to be improving but the reasons for this are unclear. They could include evolving aetiology, modifications in care, improvements in treatment or changes in lifestyle behaviour. Observational studies are required to explore survival trends and identify outcome predictors.

METHODS: We are identifying people with a new diagnosis of head and neck cancer. We obtain consent that includes agreement to collect longitudinal data, store samples and record linkage. Prior to treatment we give participants three questionnaires on health and lifestyle, quality of life and sexual history. We collect blood and saliva samples, complete a clinical data capture form and request a formalin fixed tissue sample. At four and twelve months we complete further data capture forms and send participants further quality of life questionnaires.

DISCUSSION: This large clinical cohort of people with head and neck cancer brings together clinical data, patient-reported outcomes and biological samples in a single co-ordinated resource for translational and prognostic research.

Original languageEnglish
Article number973
Number of pages6
JournalBMC Cancer
Volume14
DOIs
Publication statusPublished - 17 Dec 2014

Keywords

  • Head and neck cancer
  • Clinical cohort
  • Prognosis research
  • Patient-reported outcomes
  • Sexual history
  • Quality of life
  • Biological samples

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