Objective
Cancer patients and survivors may be disproportionately affected by COVID-19. We sought to determine the effects of the pandemic on thyroid cancer survivors’ healthcare interactions and quality of life.
Methods
An anonymous survey including questions about COVID-19 and the Patient-Reported Outcomes Measurement Information System profile (PROMIS-29, version 2.0) was hosted on the ThyCa:Thyroid Cancer Survivors’ Association, Inc. website. PROMIS scores were compared to previously published data. Factors associated with greater anxiety were evaluated with univariable and multivariable logistic regression.
Results
From 5/6/2020 – 10/8/2020, 413 participants consented to take the survey; 378 (92%) met inclusion criteria: diagnosed with thyroid cancer or NIFTP, within the United States, and completing all sections of the survey. Mean age was 53 years; 89% were female, and 74% had papillary thyroid cancer. Most respondents agreed/strongly agreed (83%) that their lives were very different during COVID-19, as was their interaction with doctors (79%). A minority (43%) were satisfied with information from their doctor regarding COVID-19 changes. Compared to pre-COVID-19, PROMIS scores were higher for anxiety (57.8 vs. 56.5, p<0.05) and lower for ability to participate in social activities (46.2 vs. 48.1, p<0.01), fatigue (55.8 vs. 57.9, p<0.01), and sleep disturbance (54.7 vs. 56.1, p<0.01). After adjusting for confounders, greater anxiety was associated with younger age (p<0.01) and change in treatment plan (p=0.04).
Conclusions
During the COVID-19 pandemic, thyroid cancer survivors reported increased anxiety compared to a pre-COVID cohort. To deliver comprehensive care, providers must better understand patient concerns and improve communication about potential changes to their treatment plans.