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1.
Cancer Control ; 27(1): 1073274820960467, 2020.
Article in English | MEDLINE | ID: covidwho-772066

ABSTRACT

Patients with lung cancer are presumed to be at high risk from COVID-19 infection due to underlying malignancy. A total of 31 COVID-19 patients with pre-diagnosed lung cancer and 186 age and sex matched COVID-19 patients without cancer in 6 hospitals in Wuhan, China were identified in our study. There was a significantly higher level of IL-6 in lung cancer group showed by multifactorial analysis. The restricted mean survival time in 10, 20, and 53 days in COVID-19 patients with lung cancer were ealier than non-cancer COVID-19 patients in the same observation time (all P values < 0.05). Our results indicated that pre-diagnosed lung cancer was associated with higher morbidity and mortality in COVID-19 patients.


Subject(s)
Betacoronavirus , Coronavirus Infections/epidemiology , Lung Neoplasms/complications , Pandemics , Pneumonia, Viral/epidemiology , COVID-19 , China/epidemiology , Coronavirus Infections/complications , Female , Hospitalization/trends , Humans , Lung Neoplasms/epidemiology , Male , Middle Aged , Pneumonia, Viral/complications , Retrospective Studies , Risk Factors , SARS-CoV-2 , Survival Rate/trends
2.
Transfusion ; 60(10): 2210-2216, 2020 10.
Article in English | MEDLINE | ID: covidwho-696126

ABSTRACT

BACKGROUND: The management of critically ill patients with coronavirus disease 2019 (COVID-19), caused by a new human virus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is challenging. Recently, there have been several reports with inconsistent results after treatment with convalescent plasma (CP) on critically ill patients with COVID-19, which was produced with a neutralizing antibody titer and tested in a P3 or P4 laboratory. However, due to the limitation of the conditions on mass production of plasma, most producers hardly had the capability to isolate the neutralizing antibody. Here, we report the clinical courses of three critically ill patients with COVID-19 receiving CP treatments by total immunoglobulin G (IgG) titer collection. METHODS: Three patients with COVID-19 in this study were laboratory confirmed to be positive for SARS-CoV-2, with radiographic and clinical features of pneumonia. CP was collected by total IgG titer of 160 (range, 200-225 mL), and patients were transfused between 20 and 30 days after disease onset at the critical illness stage as a trial in addition to standard care. The clinical courses of these patients, including laboratory results and pulmonary functional and image studies after receiving convalescent plasma infusions, were reviewed. RESULTS: No therapeutic effect of CP was observed in any of the patients; instead, all three patients deteriorated and required extracorporeal membrane oxygenation treatment. A potential cytokine storm 4 hours after infusion of CP in Patient 2 was observed. No more patients were put on the trial of CP transfusion. CONCLUSIONS: We recommend extreme caution in using CP in critically ill patients more than 2 weeks after the onset of COVID-19 pneumonia.


Subject(s)
COVID-19/therapy , SARS-CoV-2/pathogenicity , Antibodies, Neutralizing/immunology , Antibodies, Viral/immunology , Critical Illness , Humans , Immunization, Passive/methods , Immunoglobulin G/immunology , Pneumonia/immunology , Pneumonia/virology , COVID-19 Serotherapy
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