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Poster session 04

1427P - The role of anxiety and self-isolation in seropositivity for COVID-19 in actively treated cancer patients in Sweden

Date

10 Sep 2022

Session

Poster session 04

Topics

COVID-19 and Cancer;  Psychosocial Aspects of Cancer

Tumour Site

Presenters

Beatrice Ginman

Citation

Annals of Oncology (2022) 33 (suppl_7): S653-S659. 10.1016/annonc/annonc1071

Authors

B. Ginman1, S. Pahnke2, E. Freyhult3, T. Hoffman4, L. Kolstad4, B. Rönnberg4, Å. Lundkvist4, K. Hamberg5, G. Enblad6, I. Glimelius7

Author affiliations

  • 1 Department Of Immunology, Genetics And Pathology, Uppsala University, University Hospital Uppsala/Akademiska Sjukhuset, 75135 - Uppsala/SE
  • 2 Oncology/haematology, University Hospital Uppsala/Akademiska Sjukhuset, 751 85 - Uppsala/SE
  • 3 Uppsala University Hpspital, Department of Medical Sciences, Cancer Pharmacology and Computational Medicine, 75185 - Uppsala/SE
  • 4 Uppsala University, Department of Medical Biochemistry and Microbiology, 75237 - Uppsala/SE
  • 5 Uppsala University, Department of Public Health and Caring Sciences, Uppsala University, 75237 - Uppsala/SE
  • 6 Department Of Immunology, Genetics And Pathology, Uppsala University, Akademiska Sjukhuset Uppsala, 75185 - Uppsala/SE
  • 7 Department Of Immunology, Genetics And Pathology, University Hospital Uppsala/Akademiska Sjukhuset, 751 85 - Uppsala/SE

Resources

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Abstract 1427P

Background

In Sweden, recommendations to reduce the risk of COVID-19 has relied on each citizen’s own sense of responsibility rather than mandatory lockdowns. We studied how COVID-19-related anxiety and self-isolation correlated to seropositivity and PCR-positivity in Swedish patients with cancer.

Methods

In a longitudinal cohort study at Uppsala University Hospital in Sweden; 622 cancer patients on active treatment, and 358 cancer care staff were included April 1st 2020 to August 1st 2020. Serological testing for COVID-19 was done at inclusion and every 8-12-week until March 30th 2021, until vaccination started. Patients initially completed a survey regarding self-reported degree of COVID-19-related anxiety and self-isolation.

Results

622 patients were included; solid malignancy (SM) n=475, hematological malignancy (HM) n=147. 10.5% of SM patients and 6.5% of HM patients became seropositive. Staff seropositivity was higher, 16.2% (p=0.003). PCR-positivity for SM patients (n=52, 11.0%) was similar to seropositivity (n=50, 10.5%), while HM patients had higher PCR-positivity (n=14, 9.7%) than seropositivity (n=10, 6.8%). PCR-positive HM patients required more advanced in-patient treatment (67%) compared to PCR-positive SM patients (29%). High anxiety was expressed by 193 patients (31%), and no to mild anxiety by 403 (65%). Patients with SM expressed higher anxiety than those with HM (n=159, 35% vs n=34, 25%, p=0.04), but self-isolated to a similar degree (53.8% vs 57.6%). Women (OR: 3.37, 2.29-5.02, p=0.001) and patients born outside of Sweden (OR: 2.47, 1.11-5.62, p=0.027) expressed more anxiety. Patients with high anxiety were numerically less likely to test seropositive (7.2% vs 10.6%, p=0.23), while the reverse was seen for those who self-isolated (10.9% vs 8.1%, p=0.27).

Conclusions

Seroprevalence for COVID-19 among cancer patients was not impacted by a higher degree of anxiety or self-isolation in Sweden in 2020, with guidelines resembling those adopted globally today. Patients with hematological malignancies expressed less anxiety but were more likely to require advanced care if diagnosed with COVID-19, and less likely to develop an antibody response.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Lions Cancerforskningsfond SciLifeLab COVID-19.

Disclosure

I. Glimelius: Financial Interests, Institutional, I participate as scientific board on an educational event: Janssen Cilag; Financial Interests, Personal, I participate in a real-world initiative to study register-based data supported by Takeda: Takeda; Financial Interests, Personal, Safety board for evaluation of side-effects from the viral vector developed within the company: Lokon Pharma. All other authors have declared no conflicts of interest.

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