National multicentre epidemiological study to describe retrospectively and prospectively the clinical outcomes of patients with a suspected coronavirus infection (either confirmed or not) while receiving a medical treatment for the underlying cancer
Inclusion Criteria:
I1. Confirmed diagnosis of any type of solid or hematologic tumor;
I2. Ongoing anticancer treatment (cytotoxic, targeted therapy, immunotherapy or loco
regional procedure, including radiotherapy, surgery or interventional radiology procedure)
at the time of inclusion or within the last 3 months prior to inclusion (last treatment
administration or last loco regional procedure) ;
I3. Patient with suspicion of COVID-19 (clinical symptoms of COVID-19 including fever
(>38°C) and/or respiratory tract symptoms), either confirmed or not.
Note 1: Patients must have underwent diagnostic procedures: diagnostic test (positive or
negative) and/or chest imaging. Note 2: Patients will be eligible regardless of the
presence of a neutropenia (either febrile or not) ;
I4. Patient and/or family did not decline data collection after complete information.
Institut Bergonié
Bordeaux, France
Centre François Baclesse
Caen, France
Centre Hospitalier Métropole Savoie
Chambéry, France
Centre Jean Perrin
Clermont-Ferrand, France
Centre Georges François Leclerc
Dijon, France
Centre Oscar Lambret
Lille, France
Centre Leon Berard
Lyon, France
CH Annecy-Genevois
Metz-Tessy, France
Institut de Cancérologie de Montpellier
Montpellier, France
Groupement Hospitalier Porte de Provence
Montélimar, France
Centre Antoine Lacassagne
Nice, France
Centre Hospitalier Lyon-Sud
Pierre-Bénite, France
Institut Jean Godinot
Reims, France
Centre Henri Becquerel
Rouen, France
Institut de Cancérologie de l'Ouest
Saint-Herblain, France
Institut de cancérologie Strasbourg Europe (ICANS)
Strasbourg, France
Institut Universitaire du Cancer de Toulouse - IUCT Oncopole
Toulouse, France
CH Valence
Valence, France