Last update : 12/09/2020 | Version : 1 | ID : 73838
General | |
Identification | |
Detailed name | Prospective analysis of morbi-mortality of patients with cancers in active phase of treatment suspected or diagnosed of a SARS-CoV-2 infection |
Sign or acronym | ONCOVID-19 |
General Aspects | |
Medical area |
Cancer research |
Study in connection with Covid-19 |
Yes |
Pathology (details) | Any primary tumor with suspicion of SARS-CoV-2 infection |
Scientific investigator(s) (Contact) | |
Name of the director | ASSAAD |
Surname | Souad |
Organization | Centre Léon Bérard |
Collaborations | |
Participation in projects, networks and consortia |
Yes |
Funding | |
Funding status |
Mixed |
Details | Big pharma and ANR Flash COVID |
Governance of the database | |
Sponsor(s) or organisation(s) responsible | Centre Léon Bérard |
Organisation status |
Private |
Presence of scientific or steering committees |
Yes |
Additional contact | |
Main features | |
Type of database | |
Type of database |
Others |
Specify | Clinical database |
Database objective | |
Main objective |
The primary objective is to describe the mortality of cancer patients under active anticancer treatment who underwent diagnostic procedures (positive or negative) for a suspicion of COVID-19.
The primary endpoint will be the mortality rate, defined as the proportion of patients who are dead 28 days after the date of the diagnostic procedure for the 2 cohorts of patients (positive and negative). |
Inclusion criteria |
- Confirmed diagnosis of any type of solid or hematologic tumor;
- 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) ; - 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) - Patient and/or family did not decline data collection after complete information (information sheet) |
Population type | |
Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
Population covered |
Sick population |
Pathology | II - Neoplasms |
Gender |
Male Woman |
Geography area |
National |
Detail of the geography area | France (Comprehensive cancer centers, universitary hospitals and general hospitals |
Data collection | |
Dates | |
Date of first collection (YYYY or MM/YYYY) | 2020 |
Date of last collection (YYYY or MM/YYYY) | 2020 |
Size of the database | |
Size of the database (number of individuals) |
[1000-10 000[ individuals |
Details of the number of individuals | 1150 |
Data | |
Database activity |
Data collection completed |
Type of data collected |
Clinical data |
Clinical data (detail) |
Medical registration |
Details of collected clinical data | Cancer history, current cancer treatments, COVID-19 diagnosis and vital status |
Presence of a biobank |
No |
Procedures | |
Data collection method | Investigational sites |
Quality procedure(s) used | Remote monitoring |
Participant monitoring |
Yes |
Details on monitoring of participants | Day 28 (primary outcome and) Vital status update for all participants at the Last Patient Last Visit |
Links to administrative sources |
No |
Promotion and access | |
Promotion | |
Access |
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