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COVID-19 and Cancer Patients

OnCovid: Natural History and Outcomes of Cancer Patients During the COVID19 Epidemic

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04393974
Acronym
OnCovid
Enrollment
3820
Registered
2020-05-19
Start date
2020-04-01
Completion date
2024-04-01
Last updated
2026-02-17

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

Conditions

Cancer, Sars-CoV2

Brief summary

Routinely collected data will be used to assess the morbidity and mortality of cancer patients following a positive COVID-19 infection.

Detailed description

The SARS-CoV-2, (COVID-19) virus of the coronavirus family is believed to have been transmitted from animal to human. On 12th March 2020, the World Health Organisation (WHO) declared this particular coronavirus outbreak a pandemic. How COVID-19 affects people is still not widely understood. Some people who have tested positive for the virus have been asymptomatic while others, who were otherwise well and healthy before infection, have died. Currently, information obtained so far suggests that most COVID-19 illness, however older people and people with severe comorbidities such as heart and lung disease and diabetes, seem to be at higher risk of developing serious COVID-19 illness. This research is a retrospective, non-interventional study whose aim is to describe the features of COVID-19 infection specifically in cancer patients; to investigate its severity in this particular population and evaluate the long-term outcomes by means of medical charts review of consecutive patients co-diagnosed with SARS-CoV-2 infection and malignancy. Patients will be identified from electronic medical records and entered into a pre-designed database. All information used will have been previously collected as part of routine standard of care and will involve but is not limited to: blood test results, prior and current anti-cancer therapy, medical history and most importantly clinical outcomes, such as response to any treatment provided for COVID-19 and patients' survival in relation to baseline clinic-pathologic profile. All data will be collected by each patient's team and will be anonymised and stored in a password-protected NHS computer.

Interventions

None listed

Sponsors

Imperial College London
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

The investigators will evaluate and include consecutive patients observed in the outpatients and inpatients facility of the study centre meeting all the following CRITERIA: 1. Be ≥18 years of age. 2. Have a confirmed diagnosis of malignancy of any type. 3. Have a confirmed diagnosis of SARS-CoV-2 infection.

Exclusion criteria

Patients will not be entered in the study database when one or more of the following CRITERIA are present: 1. Unconfirmed diagnosis of SARS-CoV-2 infection 2. Insufficient clinical/follow up data.

Design outcomes

Primary

MeasureTime frameDescription
Describe presenting characteristics and severity or SARS-CoV-2 infection in patients with cancer2 yearsCompiling a list of symptoms experienced by patients recruited onto the trial
Assessing what factors are involved in prognosis of cancer patients with COVID-192 yearsEvaluate prognostic factors for survival in patients with SARS-CoV-2 infection and cancer

Countries

Belgium, France, Germany, Italy, Spain, United Kingdom

Contacts

PRINCIPAL_INVESTIGATORDavid J Pinato, Prof.

Clinical Professor of Experimental Cancer Therapeutics

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026