Abstract
Background
Human papillomavirus (HPV)-related cancers have been associated with different demographic profiles and disease characteristics than HPV-unrelated cancers in head and neck patients, but distress and other symptoms have not been compared. The aim of this study was to assess whether distress levels, fatigue, pain, anxiety, depression, and common psychological and practical problems differ between head and neck cancer patients with HPV-related vs. HPV-unrelated carcinomas (using oropharyngeal carcinoma (OPC) and non-OPC cancers as surrogates for HPV status).
Methods
Distress, depression, anxiety, fatigue, pain, and common problems were examined in 56 OPC and 90 non-OPC patients at 4 timepoints during the first year following diagnosis. Two-level hierarchical linear modeling was used to examine effects.
Results
The HPV-related OPC group was more likely to be younger (p = 0.05), Caucasian (p = 0.001), non-smokers (p = 0.01), earn more (p = 0.04), and present with more advanced stage (p < 0.0001). At baseline, OPC patients reported only higher pain scores (p = 0.01) than non-OPC patients. Total problems decreased more in the OPC group (p = 0.08) than the non-OPC group from baseline to 12-month follow-up. In both groups, scores on distress, depression, psychosocial problems, and practical problems decreased similarly over time.
Conclusions
Despite a difference in the clinico-demographic characteristics of HPV-related vs. HPV-unrelated patients, only baseline pain levels and total problems over time differed between the two groups.
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Acknowledgements
The collection of distress screening data was funded by the Alberta Cancer Research Institute Research Initiatives Program/Alberta Cancer Foundation.
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Contributions
MS collected the clinical data, assimilated the existing databases, and participated in drafting the manuscript. LC was involved in the design and coordination of the study, data analysis and interpretation, and as well as helped to draft the manuscript. HL participated in the design of the study and manuscript preparation. LZ performed the statistical analyses and interpretation, and drafted the methods and results section of the manuscript. BB spearheaded the collection of the distress data, reviewed, and edited the manuscript. AW participated in collection of the distress data, reviewed and edited the manuscript. SG participated in the collection the distress data, and edited the manuscript. DH conceived of the study, participated in its design and coordination and helped to draft and edit the manuscript.
All authors read and approved the final manuscript.
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The Alberta Cancer Research Ethics Committee approved this study.
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The authors declare that they have no competing interests.
Author’s information
LEC holds the Enbridge Research Chair in Psychosocial Oncology, cofunded by the Canadian Cancer Society and Alberta Cancer Foundation, and along with BDB has been responsible for developing and testing methods of implementing screening for distress as the “6th vital sign” in cancer care worldwide. The data in this paper was extracted from clinical trials which evaluated the efficacy of routine online screening for distress on subsequent psychosocial and physical outcomes.
Role of the funding source
The Alberta Cancer Research Institute Research Initiatives Program/Alberta Cancer Foundation provided funding for the collection of distress screening data used in this study.
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Schorr, M., Carlson, L.E., Lau, H.Y. et al. Distress levels in patients with oropharyngeal vs. non-oropharyngeal squamous cell carcinomas of the head and neck over 1 year after diagnosis: a retrospective cohort study. Support Care Cancer 25, 3225–3233 (2017). https://doi.org/10.1007/s00520-017-3733-5
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DOI: https://doi.org/10.1007/s00520-017-3733-5