SARS-CoV-2 seroprevalence in oncology healthcare professionals and patients with cancer at a tertiary care centre during the COVID-19 pandemic.


Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
09 2020
Historique:
received: 02 07 2020
revised: 05 08 2020
accepted: 08 08 2020
entrez: 4 9 2020
pubmed: 4 9 2020
medline: 17 9 2020
Statut: ppublish

Résumé

During the COVID-19 outbreak, healthcare professionals (HCP) are at the frontline of clinical management and at increased risk for infection. The SARS-CoV-2 seroprevalence of oncological HCP and their patients has significant implications for oncological care. HCP and patients with cancer at the Division of Oncology, Medical University of Vienna were included between 21 March and 4 June and tested for total antibodies against SARS-CoV-2 employing the Roche Elecsys Anti-SARS-CoV-2 immunoassay. Reactive samples were confirmed or disproved by the Abbott SARS-CoV-2 IgG test. Additionally, a structured questionnaire regarding basic demographic parameters, travel history and COVID-19-associated symptoms had to be completed by HCP. 146 subjects (62 HCP and 84 patients with cancer) were enrolled. In the oncological HCP cohort, 20 (32.3%) subjects were medical oncologists, 28 (45.2%) nurses at our ward and 14 (22.6%) fulfil other functions such as study coordinators. In the patient cohort, most individuals are on active anticancer treatment (96.4%). 26% of the HCP and 6% of the patients had symptoms potentially associated with COVID-19 since the end of February 2020. However, only in 2 (3.2%) HCP and in 3 (3.6%) patients, anti-SARS-Cov-2 total antibodies were detected. The second assay for anti-SARS-Cov-2 IgG antibodies confirmed the positive result in all HCP and in 2 (2.4%) patients, suggesting an initial assay's unspecific reaction in one case. In individuals with a confirmed test result, an active COVID-19 infection was documented by a positive SARS-CoV-2 RNA PCR test. Specific anti-SARS-CoV-2 antibodies were found solely in persons after a documented SARS-CoV-2 viral infection, thus supporting the test methods' high sensitivity and specificity. The low prevalence of anti-SARS-CoV-2 antibodies in our cohorts indicates a lack of immunity against SARS-CoV-2. It highlights the need for continued strict safety measures to prevent uncontrolled viral spread among oncological HCPs and patients with cancer.

Sections du résumé

BACKGROUND
During the COVID-19 outbreak, healthcare professionals (HCP) are at the frontline of clinical management and at increased risk for infection. The SARS-CoV-2 seroprevalence of oncological HCP and their patients has significant implications for oncological care.
METHODS
HCP and patients with cancer at the Division of Oncology, Medical University of Vienna were included between 21 March and 4 June and tested for total antibodies against SARS-CoV-2 employing the Roche Elecsys Anti-SARS-CoV-2 immunoassay. Reactive samples were confirmed or disproved by the Abbott SARS-CoV-2 IgG test. Additionally, a structured questionnaire regarding basic demographic parameters, travel history and COVID-19-associated symptoms had to be completed by HCP.
RESULTS
146 subjects (62 HCP and 84 patients with cancer) were enrolled. In the oncological HCP cohort, 20 (32.3%) subjects were medical oncologists, 28 (45.2%) nurses at our ward and 14 (22.6%) fulfil other functions such as study coordinators. In the patient cohort, most individuals are on active anticancer treatment (96.4%). 26% of the HCP and 6% of the patients had symptoms potentially associated with COVID-19 since the end of February 2020. However, only in 2 (3.2%) HCP and in 3 (3.6%) patients, anti-SARS-Cov-2 total antibodies were detected. The second assay for anti-SARS-Cov-2 IgG antibodies confirmed the positive result in all HCP and in 2 (2.4%) patients, suggesting an initial assay's unspecific reaction in one case. In individuals with a confirmed test result, an active COVID-19 infection was documented by a positive SARS-CoV-2 RNA PCR test.
CONCLUSION
Specific anti-SARS-CoV-2 antibodies were found solely in persons after a documented SARS-CoV-2 viral infection, thus supporting the test methods' high sensitivity and specificity. The low prevalence of anti-SARS-CoV-2 antibodies in our cohorts indicates a lack of immunity against SARS-CoV-2. It highlights the need for continued strict safety measures to prevent uncontrolled viral spread among oncological HCPs and patients with cancer.

Identifiants

pubmed: 32878898
pii: S2059-7029(20)32713-7
doi: 10.1136/esmoopen-2020-000889
pmc: PMC7470513
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e000889

Informations de copyright

© Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology.

Déclaration de conflit d'intérêts

Competing interests: TF has received honoraria for lectures, consultation or advisory board participation from the following for-profit companies: Bristol-Myers Squibb, Novartis, Roche, Sanofi, Merck Sharp & Dome, Merck Darmstadt, Amgen, Böhringer-Ingelheim, Accord, AstraZeneca. The following for-profit companies have supported clinical trials and contracted research conducted by TF with payments made to his institution: Bristol-Myers Squibb, Merck Sharp & Dome, Roche, Merck Darmstadt. ASB has research support from Daiichi Sankyo (≤€10 000), Roche (>€10 000) and honoraria for lectures, consultation or advisory board participation from Roche, Bristol-Meyers Squibb, Merck, Daiichi Sankyo (all <€5000) as well as travel support from Roche, Amgen and AbbVie. ASB has research support from Daiichi Sankyo (≤€10 000), Roche (>€10 000) and honoraria for lectures, consultation or advisory board participation from Roche, Bristol-Meyers Squibb, Merck, Daiichi Sankyo (all <€5000) as well as travel support from Roche, Amgen and AbbVie. MP has received honoraria for lectures, consultation or advisory board participation from the following for-profit companies: Bayer, Bristol-Myers Squibb, Novartis, Gerson Lehrman Group (GLG), CMC Contrast, GlaxoSmithKline, Mundipharma, Roche, BMJ Journals, MedMedia, AstraZeneca, AbbVie, Lilly, Medahead, Daiichi Sankyo, Sanofi, Merck Sharp & Dome, Tocagen. The following for-profit companies have supported clinical trials and contracted research conducted by MP with payments made to his institution: Böhringer-Ingelheim, Bristol-Myers Squibb, Roche, Daiichi Sankyo, Merck Sharp & Dome, Novocure, GlaxoSmithKline, AbbVie. GH, TP, RS, JB, HCP, JK, FM, LS, AMS, AS, SW and ST have nothing to disclose.

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Auteurs

Thorsten Fuereder (T)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Anna Sophie Berghoff (AS)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Gerwin Heller (G)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Helmuth Haslacher (H)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Thomas Perkmann (T)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Robert Strassl (R)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Julia Maria Berger (JM)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Hannah Christina Puhr (HC)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Judith Kreminger (J)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Florian Moik (F)

Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Lorenz Schubert (L)

Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria.

Angelika Martina Starzer (AM)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Ariane Steindl (A)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Stefan Winkler (S)

Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria.

Matthias Preusser (M)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Selma Tobudic (S)

Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria. Electronic address: selma.tobudic@meduniwien.ac.at.

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Classifications MeSH