Literature DB >> 32434108

Cancer treatment during the coronavirus disease 2019 pandemic: Do not postpone, do it!

Claudia Omarini1, Michela Maur2, Gabriele Luppi2, Franco Narni3, Mario Luppi3, Massimo Dominici4, Giuseppe Longo2, Federico Piacentini4.   

Abstract

At the end of January 2020, a novel betacoronavirus, known as severe acute respiratory syndrome coronavirus 2, progressively spread in Italy. Patients with cancer are considered more prone to infections because of the immunosuppressive status due to both malignancy and anticancer treatments. From the first Italian government restrictions (23rd February), Modena Cancer Center adopted practical health vigilance recommendations to minimise the risk of exposure to the virus without overlooking cancer management. From 23rd February to 31st March 2020, 1257 patients on active anticancer treatment for oncological or haematological malignancies attended our institution. All the staff activities were rescheduled following our practical coronavirus disease 2019 (COVID-19) guideline. During this period, we have tallied 9 cases of COVID-19 infection (0.71%) in patients with cancer and 3 cases (1.66%) in health workers. The mortality rate of our patients with cancer was 22%, consistent with the data reported in the literature. In conclusion, following our practical health vigilance recommendations, physicians should be confident in maintaining life-saving anticancer treatment without exceedingly increasing the risk of nosocomial COVID-19 infection. The high rate of mortality suggested that all patients on active anticancer treatment with flu-like symptoms have to be carefully screened for COVID-19 infection.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  COVID-19; Cancer care; Pandemic; Practical health vigilance recommendations; SARS-CoV-2

Mesh:

Year:  2020        PMID: 32434108      PMCID: PMC7214318          DOI: 10.1016/j.ejca.2020.04.034

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


At the end of January 2020, a novel betacoronavirus known as severe acute respiratory syndrome coronavirus 2 progressively spread in Italy. Outside China, Italy was the most affected by the coronavirus disease 2019 (COVID-19) outbreak, with 105792 confirmed cases and 12428 deaths, as of 31st March 2020 [1]. Emilia-Romagna is the second most involved region in Italy, with overall 14074 cases registered at the end of March 2020 in Modena. To limit viral spread, the Italian government implemented extraordinary measures from 23rd February to 9th March, culminating with the lockdown of all social and work activities unless strictly required. Patients with cancer are considered more prone to infections because of the immunosuppressive status due to both malignancy and anticancer treatments [2]. A national analysis performed in China showed that patients with cancer have five times higher risk of COVID-19 infection as well as a higher risk of severe events and greater need for intensive care assistance than patients without cancer [3]. For these reasons, the authors proposed three major strategies: postpone adjuvant therapies and elective surgery, use stronger personal protection provisions for patients with cancer/survivors and consider intensive surveillance in infected patients [3]. In addition, a retrospective cohort study published by Zhang et al [4] identified that anticancer therapies within 14 days from infection was an independent predictor of death or other severe events, with a hazard ratio higher than 4. Actually, the issue on how to manage cancer care during the COVID-19 pandemic is crucial. From the first Italian government restrictions (23rd February 2020), Modena Cancer Center adopted practical health vigilance recommendations to minimise the risk of exposure to the virus without overlooking cancer management. Of note, we halted everything for a few days to analyse the situation and develop the following plan. Patient care Provide surgical face masks and access to cleaning/disinfecting agents for all people having access to the clinic. Contact the patient on active anticancer treatment the day before the appointment for screening of symptoms of cough, sore throat, fever or other flu-like symptoms. Patient with symptoms must be rescheduled. Allow access to visitors only if essential to visit. Prohibit visitors' access to the haemopoietic stem cell transplantation unit and to the inpatient haematology ward. Increase interval between visits to reduced waiting time. Postpone routine follow-up visits for patients not on active cancer treatment (e.g. 6- to 12-month survivorship visits), and conduct appointments via telemedicine. Respect lifestyle restrictions. Facility reorganisation Limit access to the hospital through one point of entry. Establish triage stations outside the hospital to screen patients and visitors for COVID-19 symptoms. Convert the waiting area to allow for distancing of at least 1 m. Dedicate a confined hospital area for patients with respiratory symptoms who present to the oncological/haematological admission room (e.g. COVID-19 room). Staff Provide personal protective equipment (PPE) (e.g. surgical face mask) and access to cleaning/disinfecting agents for all the staff members. Train clinic staff for symptom recognition, screening procedures and PPE use. Reduce the number of non-medical staff in the clinic by allowing work from home for phone-based activities. Organise Web-based multidisciplinary team meetings. Respect lifestyle restrictions. From 23rd February to 31st March 2020, 1257 patients on active anticancer treatment attended our institution, 93% of whom were on an outpatient setting. All staff activities were rescheduled following our practical COVID-19 guideline. During this period, only 9 patients were diagnosed as having symptomatic COVID-19 infection corresponding to 0.71% of patients on active anticancer drugs treated in our hospital. All of them received their anticancer treatments as outpatients. Patient characteristics and clinical outcomes of COVID-19 infections are summarised in Table 1 . In particular, 5 patients had haematological malignancy, while 4 had an active solid tumour. The median age was 74 years (range = 65–86 years), and all had co-morbidities other than cancer. Considering time from the last visit/treatment and the onset of COVID-19 symptoms, in two-thirds of patients, a nosocomial transmission could not be excluded. All but one required hospitalisation owing to rapid deteriorating conditions. Two of them (22%) died owing to COVID-19 infection, both with gastrointestinal solid tumour.
Table 1

Characteristics and clinical outcome of COVID-19–infected patients.

GenderAgeType of cancerCo-morbiditiesAnticancer treatmentTime from thelast visit to the onset of COVID-19 symptoms, daysSymptomsComplicationsOutcomea
Patient 1F69Urothelial carcinoma (stage IV)HypertensionAnti-TIGITb – pembrolizumab7Cough, feverPneumoniaHospitalisation
Patient 2M73Acute promyelocytic leukaemiaGallbladder cancer (stage IV), atrial fibrillation, hypertensionRetinoic acid8FeverPneumoniaHospitalisation
Patient 3F65Pancreatic cancer (stage III)Chronic liver diseaseFolfirinoxc7Dyspnoea, feverARDSDeath
Patient 4F75Salivary gland cancer (stage IVB)Breast cancerRadiotherapyNot applicabledFlu-like symptomsNoneHome self-isolation
Patient 5F86Chronic lymphatic leukaemiaChronic liver disease, hypertensionIbrutinib33Cough, feverPneumoniaHospitalisation
Patient 6M76Mantle cell lymphomaProstate cancer, cardiovascular diseaseIbrutinib21Cough, feverARDSDischarge from the hospital
Patient 7M72Chronic lymphatic leukaemiaHypertension, obesityBendamustine-rituximab10FeverNoneDischarge from the hospital
Patient 8M73Follicular lymphomaCardiovascular diseaseRituximab17FeverPneumoniaHospitalisation
Patient 9M75Colorectal cancerCardiovascular diseaseCapecitabine-bevacizumab14Fever, mental confusionARDSDeath

COVID-19 = coronavirus disease 2019; TIGIT = T-cell immunoreceptor with immunoglobulin and ITIM domains; ARDS = acute respiratory distress syndrome.

At the time of manuscript submission.

Immune checkpoint inhibitors.

Fluorouracil, irinotecan and oxaliplatin.

The patient was on radiotherapy started 23 days before.

Characteristics and clinical outcome of COVID-19infected patients. COVID-19 = coronavirus disease 2019; TIGIT = T-cell immunoreceptor with immunoglobulin and ITIM domains; ARDS = acute respiratory distress syndrome. At the time of manuscript submission. Immune checkpoint inhibitors. Fluorouracil, irinotecan and oxaliplatin. The patient was on radiotherapy started 23 days before. Evidence from our experience suggested that the practical health recommendations adopted in our hospital significantly decrease the risk of nosocomial COVID-19 infection in patients with cancer under active treatment. In our opinion, cancer care cannot be postponed only on the basis of the risk of COVID-19 infection. Physicians should take into account the patient's age and clinical needs, co-morbidities and life expectancy when choosing a cancer treatment even during the COVID-19 pandemic. Of note, our study population also included patients on immunosuppressive treatment for haematological malignancies, who are well known to have a more profound immunosuppressive status than those with solid tumour, reinforcing the value and positive impact of our recommendations. The beneficial effects of the extensive use of surgical masks by patients and staff members have recently and formally been demonstrated too [5]. Moreover, our strict restrictions have kept workers safe and have limited the spread of COVID-19 infection among healthcare personnel too. In particular, we have tallied only 3 cases of COVID-19 infection in health workers, corresponding to 1.66% of the Modena Cancer Center medical staff. Despite the small number of infected patients, the rate of mortality was higher than that of the population without cancer of the same age (22% in our study population vs 8.0% in patients without cancer aged 70–79 years and 14.8% in those aged ≥80 years) [6]. The mortality rate of our patients, as well as the incidence of severe events, is consistent with the data reported in the literature (22% vs 28%) [7]. All but one of our patients developed serious complications that required hospitalisation. For that reason, we are concordant to carefully screen for COVID-19 infection in all patients on active anticancer treatment with flu-like symptoms. Therefore, we propose to apply our practical health vigilance recommendations in all cancer centres. Following these advices, physicians should be confident in maintaining life-saving anticancer treatment without exceedingly increasing the risk of nosocomial COVID-19 infection. Moreover, by considering the high rate of mortality and/or severe complications, intensive attention should be paid to patients with cancer and COVID-19 symptoms/infection.

Conflict of interest statement

None.
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