A2 Refereed review article in a scientific journal

Psychological Factors Related to Treatment Outcomes in Head and Neck Cancer




AuthorsMäkitie, Antti A.; Alabi, Rasheed Omobolaji; Pulkki-Råback, Laura; Almangush, Alhadi; Beitler, Jonathan J.; Saba, Nabil F.; Strojan, Primoz; Takes, Robert; Guntinas-Lichius, Orlando; Ferlito, Alfio

PublisherSPRINGER

Publishing placeNEW YORK

Publication year2024

JournalAdvances in Therapy

Journal name in sourceADVANCES IN THERAPY

Journal acronymADV THER

Volume41

First page 3489

Last page3519

Number of pages31

ISSN0741-238X

eISSN1865-8652

DOIhttps://doi.org/10.1007/s12325-024-02945-3

Web address https://doi.org/10.1007/s12325-024-02945-3

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/457575513


Abstract

Background

Patients with head and neck cancer (HNC) often demonstrate stress, distress, anxiety, depression, and are at risk for suicide. These affect their quality of life (QoL) but less attention has been given to psychological variables that may impact response to treatment.

Objectives

This study aims to systematically review publications during 2013-2023 to collate evidence on the effects of psychological variables on HNC treatment outcomes.

Methods

We searched Ovid Medline, PubMed, Scopus, and Web of Science for articles that examined psychological factors related to treatment outcomes in patients with HNC.

Results

There were 29 studies (5 before treatment, 2 during, 17 after, and 5 covering the whole management trajectory) including 362,766 patients. The psychological factors were either behavioral (adjustment and coping strategy, unrealistic ideas, self-blame), cognitive (elevated risk of psychiatric co-comorbidity), or emotional (distress, depression, anxiety, nervousness, and fear of disfigurement and complications). It was found that there was a relationship between depression and decreased survival in patients with HNC. Pretreatment pain was an independent predictor of decreased survival in a large sample of patients. The distress level was approximately 54%, emotional problems ranged between 10 and 44%, while financial difficulties were identified in 54% of the patients. Sixty-nine percent of patients were reported to have used at least one cost-coping strategy within 6 months after treatment initiation. During post-treatment period, depression increased from 15% at the baseline to 29%, while the fear of recurrence was found among at least 35% of patients.

Discussion and Conclusion

Several psychological factors predict QoL and survival among HNC survivors. Distress encompasses depression and anxiety, and physical burden from HNC diagnosis and treatment. Routine screening and early interventions that target distress could improve HNC survivors' QoL. A systematic and standardized measurement approach for QoL is warranted to homogenize these findings and to understand the underlying relationships.


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Funding information in the publication
Open Access funding provided by University of Helsinki (including Helsinki University Central Hospital). This review was funded by the Sigrid Jusélius Foundation (M.A), the Helsinki University Hospital Research Fund (M.A), Turku University Hospital Fund (A.A), the Gyllenberg Foundation, and the Juho Vainio Foundation (L.P-R). No funding or sponsorship was received for the publication of this article.


Last updated on 2025-27-01 at 20:02