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A comprehensive assessment protocol including patient reported outcomes, physical tests, and biological sampling in newly diagnosed patients with head and neck cancer: is it feasible?

Authors :
C. René Leemans
Remco de Bree
Laurien M. Buffart
Boudewijn J.M. Braakhuis
Ruud H. Brakenhoff
Annette J. van Nieuwenhuizen
Irma M. Verdonck-de Leeuw
Jan Smit
Clinical Psychology
EMGO+ - Musculoskeletal Health
Otolaryngology / Head & Neck Surgery
Epidemiology and Data Science
Psychiatry
EMGO - Musculoskeletal health
CCA - Quality of life
Source :
Supportive Care in Cancer, Supportive Care in Cancer, 12(22), 3321-3330. Springer Verlag, van Nieuwenhuizen, A J, Buffart, L M, Smit, J H, Brakenhoff, R H, Braakhuis, B J, de Bree, R, Leemans, C & Verdonck-de Leeuw, I M 2014, ' A comprehensive assessment protocol including patient reported outcomes, physical tests, and biological sampling in newly diagnosed patients with head and neck cancer: is it feasible? ', Supportive Care in Cancer, vol. 12, no. 22, pp. 3321-3330 . https://doi.org/10.1007/s00520-014-2359-0
Publication Year :
2014
Publisher :
Springer Berlin Heidelberg, 2014.

Abstract

Purpose Large cohort studies are needed taking into account cancer-related, personal, biological, psychobehavioral, and lifestyle-related factors, to guide future research to improve treatment and supportive care. We aimed to evaluate the feasibility of a comprehensive baseline assessment of a cohort study evaluating the course of quality of life (QoL). Methods Newly diagnosed head and neck cancer (HNC) patients were asked to participate. Assessments consisted of questionnaires (635 items), a home visit (including a psychiatric interview, physical tests, and blood and saliva collection), and tissue collection. Representativeness of the study sample was evaluated by comparing demographics, clinical factors, depression, anxiety, and QoL between responders and non-responders. Feasibility was evaluated covering the number of questions, time investment, intimacy, and physical burden. Results During the inclusion period (4 months), 15 out of 26 (60 %) patients agreed to participate. Less women participated, 13 % in responders group versus 63 % in non-responders group (p = 0.008). No other differences were found between responders and non-responders. Responders completed more than 95 % of the questionnaires’ items and rated the number of questions, time investment and intimacy as feasible, and the physical and psychological burden as low. It took on average 3 h to complete the questionnaires and 1.5 h for the home visit. Conclusions This study reveals that a comprehensive assessment including various questionnaires, physical measurements, and biological assessments is feasible according to patients with newly diagnosed HNC. A large prospective cohort study has started aiming to include 739 HNC patients and their informal caregivers in the Netherlands.

Details

Language :
English
ISSN :
14337339 and 09414355
Volume :
22
Issue :
12
Database :
OpenAIRE
Journal :
Supportive Care in Cancer
Accession number :
edsair.doi.dedup.....0a0ae25a9eb95a94d14c427a7f15d324
Full Text :
https://doi.org/10.1007/s00520-014-2359-0