COVID, Lung Cancer, SARS-CoV 2
Conditions
Keywords
Diagnostic management, Therapeutic management
Brief summary
The unexpected onset of SARS-COV2 infection modified our practices, especially in routine medicine. In order to reverse the epidemic curve of severe cases and slow the spread of the infection, confinement was generalized in France from March 13, 2020.These restrictive measures were imposed on anyone with symptoms compatible with the infection, with the exception of dyspnea and other criteria of severity. March 12, 2020 is the pivotal date when the management of COVID came to interfere with medical and healthcare organizations. From this date, it is likely that some imaging or endoscopic exams have been de-scheduled for symptoms that are sometimes wrongly judged to be non-urgent and have seen their numbers drop dramatically.Otherwise, concerning lung cancer, preventive measures have been extremely strengthened. For instance, it is recommended to delay surgeries for localized tumors, to relieve or remove some chemotherapy or to delete radiotherapy sessions deemed non-essential. However, symptoms that may initially be attributed to viral infection, such as cough, fever, fatigue, or chest pain may be clinical indicators of early-stage Lung cancer. In addition, lung cancer is likely to make the patient more susceptible to pneumopathy, due to a weakened of immune response to viruses and bacteria. Consequently, as necessary as the restriction measures are, a risk of slowing down in the management of the Lung cancer pathology exists. The CBP-COVID Study intends to assess consequences of restrictive measures linked to the SARS-COV2 epidemic, by comparing clinical characteristics at diagnosis, treatment times and treatments, regarding to 2 distinct time periods identical to the calendar, but one in 2019, the other in 2020.
Interventions
None listed
Sponsors
ONCO PAYS de la LOIRE
Centre Hospitalier le Mans
Study design
Observational model
OTHER
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient newly diagnosed with a lung cancer based on histological or cytological criteria. * Patient followed by investigating site participating in the study. * Patient informed verbally and by an information document specifying the interest of the study and having given his oral agreement for the participation for the prospective part of the study.
Exclusion criteria
* Patient investigated and / or monitored in a site not involved in the study. * Patient with lung cancer of incidental finding during hospitalization for another reason. * Patient with recurrence of a previoulsy known lung cancer. * Patient included in a clinical research trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Comparison of clinical characteristics | At the end of the second period, i.e. on August 28, 2020 | Comparison Group 2019 versus Group 2019 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Comparison of diagnostic procedures | At the end of the second period, i.e. on August 28, 2020 | Comparison Group 2019 versus Group 2020 |
| Comparison of treatments (according to stage of disease) | At the end of the second period, i.e. on August 28, 2020 | Comparison Group 2019 versus Group 2020 |
| Comparison of patients management deadlines | At the end of the second period, i.e. on August 28, 2020 | Comparison Group 2019 versus Group 2020 |
| Comparison of survival | After 2 years post diagnoses | Comparison Group 2019 versus Group 2020 |
Countries
France
Contacts
Primary ContactCHRISTELLE JADEAU
Backup ContactOLIVIER MOLINIER, MD
Outcome results
None listed