key: cord-0709052-l3chn9yq
authors: Berger, Julia M.; Gansterer, Margaretha; Trutschnig, Wolfgang; Bathke, Arne C.; Strassl, Robert; Lamm, Wolfgang; Raderer, Markus; Preusser, Matthias; Berghoff, Anna S.
title: SARS-CoV-2 screening in cancer outpatients during the second wave of the COVID-19 pandemic: Conclusions for crisis response at a high-volume oncology center
date: 2021-08-19
journal: Wien Klin Wochenschr
DOI: 10.1007/s00508-021-01927-7
sha: a9d4b59b903be4af671807a37e4098054f6ad42a
doc_id: 709052
cord_uid: l3chn9yq

BACKGROUND: During the second wave of the coronavirus disease 2019 (COVID-19) pandemic Austria suffered one of the highest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) rates worldwide. We report performance parameters of a SARS-CoV‑2 screening program established for cancer outpatients at our center. METHODS: Institutional policy recommended routine biweekly SARS-CoV‑2 testing. Adherence to the testing recommendation during the second wave of the COVID-19 pandemic between 1 October and 30 November 2020 was analyzed. The SARS-CoV‑2 infection rate during first wave period (21 March to 4 May 2020) was compared to the one during second wave. RESULTS: A total of 1577 cancer patients were seen at our outpatient clinic during the second wave. In 1079/1577 (68.4%) patients, at least 1 SARS-CoV2 test was performed. Overall 2833 tests were performed, 23/1577 (1.5%, 95% confidence interval, CI 1.0–2.2%) patients were tested positive for SARS-CoV‑2, which indicates a significant increase compared to the first wave (4/1016; 0.4%, 95% CI 0.1–1.0%) with an odds ratio of 3.9 (95% CI 1.5–10.1; p < 0.005). Patients undergoing active anticancer treatment (172/960; 17.9% not tested) were more likely to have undergone a SARS-CoV‑2 test than patients in follow-up or best supportive care (326/617; 52.8% not tested p < 0.001). Furthermore, patients with only 1 visit within 4 weeks were more likely to not have undergone a SARS-CoV‑2 test (386/598; 64.5%) compared to patients with 2 or more visits (112/979; 11.4%; p < 0.001). The projected number of patients with undetected SARS-CoV‑2 infection during the study period was 5. CONCLUSION: We identified clinical patient parameters influencing SARS-CoV‑2 testing coverage in cancer outpatients. Our data can provide information on generation of standard operating procedures and resource allocation during subsequent infection waves.

The coronavirus disease 2019 (COVID-19) pandemic has caused a global health crisis and caused over 1,532,418 deaths worldwide until 7 December 2020 [1] . Oncology patients were repetitively reported to be at a particular risk with fatality rates of up to 11.4% [2] [3] [4] . Potential factors contributing to the higher risk for adverse COVID-19 courses among cancer patients include the high average age, high rate of comorbidities, disease-associated and therapy-induced immunosuppression and unavoidable social contacts during regular therapy and follow-up visits at the hospital [5] ; however, besides direct endangerment of cancer patients by severe acute respiratory K SARS-CoV-2 screening in cancer outpatients during the second wave of the COVID-19 pandemic original article syndrome coronavirus 2 (SARS-CoV-2) infections, concerns about adverse outcomes associated with disruptions in oncological care due to COVID-19 have emerged [6, 7] . Therefore, continued administration of anti-cancer therapies has been defined as a priority by oncological societies and cancer centers around the world [8, 9] .

At our large tertiary care center of medical oncology with approximately 40,000 patient contacts per year, we have rapidly implemented strict safety measures during the first wave of the COVID-19 pandemic in Spring 2020. We could show that these safety precautions resulted in low rates of detectable SARS-CoV-2 infections among our patients and anti-SARS-CoV-2 antibodies among our patients and staff that allowed continued patient care and therapy at our center [10, 11] .

The second wave of the COVID-19 pandemic in the fall of 2020 hit Austria particularly hard as Austria was among the countries with the highest 7-day incidence rates worldwide with 565 new infections per 100,000 on 12 November 2020 [12] . In order to protect the well-being of our patients and staff as well as the functionality of our clinical service, we implemented strict safety measures during the second wave based on our experience during the first wave. Although many institutions refrained from regular SARS-CoV-2 testing of patients owing to logistic restraints, the safety measures implemented at our institution included a recommendation for biweekly testing of all patients for SARS-CoV-2 RNA using nasopharyngeal swabs and polymerase chain reaction (PCR).

Here, we analyzed performance parameters of this SARS-CoV-2 screening program at our center during the second wave. We aim to provide an information basis for optimization of standard operating procedures and resource allocation for crisis response during potential subsequent infection waves of the COVID-19 pandemic.

This study was approved by the ethics committee of the Medical University of Vienna (vote number 2485 of 2020).

All patients treated at the outpatient department of the Division of Oncology, Department of Medicine 1, Medical University of Vienna between 1 October and 30 November 2020 were included in this retrospective analysis. During this period, only outpatients without COVID-19 symptoms were permitted access to our department and our institutional policy recommended routine biweekly real-time polymerase chain reaction-based SARS-CoV-2 testing. Testing was performed by PCR test only. Further safety measurements and the date of implementation are listed in Table 1 . A patient cohort treated at our department and tested for SARS-CoV-2 during the first wave of the COVID-19 pandemic between 21 March and 4 May 2020 was available for comparison [10] .

Testing for SARS-CoV-2 viral RNA was exclusively performed by nasal or pharyngeal swabs and real-time polymerase chain reaction (RT-PCR). RT-PCR analysis was either performed using an european conformity in-vitro diagnostics (CE/IVD) validated workflow (Cobas SARS-CoV-2 assay on the Roche Cobas 6800 platform [Roche, Basel, Switzerland]; Abbott Re-alTime SARS-CoV-2 assay on the Abbott m2000 platform [Abbott, Chicago, IL, USA]) or using a validated RT-PCR workflow according to Corman et al. [13] . The rate of false positive results is estimated at 0.04% whereas the rate of false positive tests is estimated at 0.0-1.0% [14] [15] [16] . All analyses were carried out at the Department of Laboratory Medicine, Division of Clinical Virology, Medical University of Vienna, Vienna, Austria. Comparability of the results of all test methods was demonstrated by participating in the international quality control ring trials [17] .

The first wave was defined from 21 March to 10 May 2020. Table 2 .

During the second wave period, a total of 2833 SRAS-CoV-2 tests were performed in 1577 patients and 1079/1577 (68.4%) patients were tested at least once during the observation period (Fig. 1a) Fig. 1d ).

During the second wave period, SARS-CoV-2 was detected in 23 The detection rate of 23/1577 (1.5%, 95% confidence interval, CI 1.0-2.2%) indicates a significant increase of infections compared to the first wave in spring 2020 (4/1016; 0.4%, 95% CI 0.1-1.0%). Among patients at our institution, the odds ratio for comparison of positive tests in the second versus the first wave was 3.9 (95% CI 1.5-10.1; p < 0.005). (Fig. 2a) .

The projected number of patients with undetected SARS-CoV-2 infection during the second wave at our department was five.

In the Austrian population 12,717/266,354 (4.8%) individuals were tested positive for SARS-CoV-2 in the first wave period compared to 238,628/1,241,703 Fig. 1 a Patients according to performed test; b median age in tested and not tested patients; c median number of visits of tested and not tested patients; d therapy status in tested and not tested patients; e distribution of patients with SARS CoV-2 infection according to primary tumor. ns not significant, *** p < 0.001 (19.2%) individuals during the second wave period. In the Austrian population, the odds ratio for comparison of positively tested patients in the second versus the first wave was 4.0 (95% CI 4.0-4.1; p < 0.001). (Fig. 2b ) Therefore, both in the general Austrian population as well as in the cancer cohort the odds to be infected with SARS-CoV-2 in the second wave were approximately 4 times higher than in the first wave.

SARS-CoV-2 testing is essential to prevent viral transmission and curb the on-going pandemic by early identification and isolation of infected individuals. Due to the incubation period of 3-6 days, asymptomatic virus carriers are major contributors to the overall viral spread, particularly in the setting of healthcare facilities [19] [20] [21] [22] . Consequently, focused testing in healthcare facilities is recommended to prevent nosocomial COVID-19 infections and maximize safety of patients and staff [19] . In the present data we observed comparable increases in SARS-CoV-2 infections in the cancer cohort as in the general Austrian population. We achieved a 68.4% testing coverage of cancer outpatients treated at our department during the second wave of the COVID-19 pandemic between October 1st and November 30th using an institutional policy recommending biweekly SARS-CoV-2 testing. Our strategy is based on our previously reported experience [10] and differs from other centers that perform SARS-CoV-2 testing only in selected patients [21, [23] [24] [25] .

SARS-CoV-2 screening in cancer outpatients during the second wave of the COVID-19 pandemic K original article Overall, our data indicate that routine PCR-based testing is feasible at a large department of medical oncology with over 3000 patient contacts per month; however, perfect test coverage was not achieved, leading to a projected number of five undetected virus carriers at our department during the observation period. We report that clinical patient parameters apparently influenced SARS-CoV-2 testing rate in cancer in a high-volume setting. We believe that our data may be useful for adaptation of standard operating procedures and resource allocation in order to optimize protective measures during potential subsequent infection waves of the COVID-19 pandemic.

Patients currently not under active antineoplastic treatment and patients with a lower number of visits were less likely to undergo SARS-CoV-2 testing. The experience gathered during the observation period indicates that logistical challenges are main contributors to limiting full test coverage of all patients. The infrastructure of our institution did not allow for direct easy access testing during patient presentation at our department but necessitated the referral of patients to a central SARS-CoV-2 testing unit that services the entire hospital. The implementation of a central testing unit allows efficient resource allocation and standardized testing at a large center; however, it increases the complexity of patient administration for staff members and the number of in-hospital transits and waiting times for individual patients. These factors likely have contributed to our results and need to be taken into account for informed application of safety measures to contain viral spread. As a consequence of our data, we advocate routine extramural testing of patients not undergoing active anticancer therapy just before presentation to a tertiary care oncology service, e.g. at general practitioners or testing facilities for the general public. In-hospital testing should be reserved for patients undergoing active anticancer therapy in order to achieve focused resource allocation. This measure should be suitable to avoid underdetection of SARS-CoV-2 positive patients in the vulnerable medical oncology center and thus increase patient and staff safety [26] . Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

WHO Coronavirus disease (COVID-19) dashboard

Patients with cancer appear more vulnerable to SARS-coV-2: a multicenter study during the COVID-19 outbreak

Cancer patients in SARS-CoV-2 infection: a nationwide analysis in China

Determinants of the outcomes of patients with cancer infected with SARS-CoV-2: results from the Gustave Roussy cohort

Risk of COVID-19 for cancer patients

Impact of COVID-19 on cancer care: how the pandemic is delaying cancer diagnosis and treatment for American seniors

The impact of COVID-19 on cancer screening: challenges and opportunities

Delivering cancer care during the COVID-19 pandemic: recommendations and lessons learned from ASCO global webinars

Managing cancer patients during the COVID-19 pandemic: an ESMO multidisciplinary expert consensus

SARS-coV-2 testing in patients with cancer treated at a tertiary care hospital during the COVID-19 pandemic

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

Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eurosurveillance

Estimating the false positive rate of highly automated SARS-CoV-2 nucleic acid amplification testing

Variability of cycle threshold values in an external quality assessment scheme for detection of the SARS-CoV-2 virus genome by RT-PCR

First results of a national external quality assessment scheme for the detection of SARS-CoV-2 genome sequences

Verification and validation of diagnostic laboratory tests in clinical virology

Daten Datenplattform COVID

Laboratory testing strategy recommendations for COVID-19: Interim guidance

Managing cancer patients during the COVID-19 pandemic: an ESMO multidisciplinary expert consensus

COVID-19 testing in patients with cancer: does one size fit all?

Importation and human-to-human transmission of a novel Coronavirus in Vietnam

Testing for COVID-19 in lung cancer patients

Cancer patient management strategy in a Cancer Center of Zhejiang, China during the COVID-19 pandemic

Recommendations for testing and treating outpatient cancer patients in the era of COVID-19

Underdetection of COVID-19 cases in France threatens epidemic control