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Prospective Analysis of Morbi-mortality of Patients With Cancers in Active Phase of Treatment Suspected or Diagnosed of a SARS-CoV-2 Infection

Prospective Analysis of Morbi-mortality of Patients With Cancers in Active Phase of Treatment Suspected or Diagnosed of a SARS-CoV-2 Infection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04363632
Acronym
ONCOVID-19
Enrollment
1231
Registered
2020-04-27
Start date
2020-04-02
Completion date
2020-06-30
Last updated
2020-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Sars-CoV2

Keywords

COVID-19, Oncology, Epidemiology, Predictive factors

Brief summary

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

Interventions

None listed

Sponsors

Centre Leon Berard
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Mortality of cancer patients under active anticancer treatment28 days after the date of the diagnostic procedureMortality 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).

Secondary

MeasureTime frameDescription
Patients' characteristicsAt the date of the diagnostic procedureTo describe accurately patients' characteristics in terms of demographics
Overall survival6 months (i.e. at the the time of last patient last visit)Overall survival will be defined as the time from the date of the first diagnostic procedure (either diagnostic test or chest imaging) to the date of death due to any cause.
Hospitalizations28 days after the date of the diagnostic procedureThe duration of hospitalization (from the date of hospitalization to the date of definitive discharge for live patients)
Death6 months (i.e. at the the time of last patient last visit)Cause of death, related or not to the COVID-19
Complications28 days after the date of the diagnostic procedureAssociated complications described by their type

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026