Tracking lung cancer treatment evolution in France since 2015
Epidemiological Strategy and Medical Economic (ESME) Research Program / Academic Real World Data Platform: Evolution of the Therapeutic Care in Lung Cancer in France Since 2015
This study is collecting and organizing information from lung cancer patients in France to see how their treatments have changed and what outcomes they have experienced since 2015.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 70000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Unicancer Academic / other |
| Locations | 21 sites (Angers and 20 other locations) |
| Trial ID | NCT03848052 on ClinicalTrials.gov |
What this trial studies
This observational study compiles data from electronic medical records of lung cancer patients treated at 38 hospitals across France, including comprehensive cancer centers and public hospitals. It focuses on collecting detailed information about patient demographics, tumor characteristics, treatment protocols, and clinical events. Trained technicians gather and harmonize this data using a centralized electronic data collection tool, ensuring that all information is anonymized and aggregated for analysis. The aim is to create a comprehensive database that reflects real-world treatment outcomes and trends in lung cancer care.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 who have been treated for lung cancer or diagnosed with metastatic lung cancer at one of the participating sites.
Not a fit: Patients who have not received treatment for lung cancer or those under 18 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of lung cancer treatments and improve patient care strategies.
How similar studies have performed: Other observational studies have successfully utilized real-world data to inform treatment practices, suggesting that this approach is both valid and valuable.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria : * Adult (over 18) * Treated (with radiotherapy or systemic anti-cancer treatment) for a lung cancer or diagnosed with metastatic lung cancer over the selection period at one of the participating site Exclusion criteria \- None
Where this trial is running
Angers and 20 other locations
- Institut de Cancérologie de l'Ouest - Paul Papin — Angers, France (Recruiting)
- Institut Bergonié — Bordeaux, France (Recruiting)
- Centre François Baclesse — Caen, France (Recruiting)
- Centre Jean Perrin — Clermont-Ferrand, France (Recruiting)
- Hôpital Intercommunal de Créteil — Créteil, France (Recruiting)
- Centre Georges-François Leclerc — Dijon, France (Recruiting)
- Centre Oscar Lambret — Lille, France (Recruiting)
- Centre Léon Bérard — Lyon, France (Recruiting)
- Institut Paoli-Calmettes — Marseille, France (Recruiting)
- Institut régional du Cancer Montpellier / Val d'Aurelle — Montpellier, France (Recruiting)
- Groupe Hospitalier Région Mulhouse et Sud Alsace - Hôpital Emile Muller — Mulhouse, France (Recruiting)
- Institut de cancérologie de l'Ouest - René Gauducheau — Nantes, France (Recruiting)
- Centre Antoine Lacassagne — Nice, France (Recruiting)
- Institut Curie — Paris, France (Recruiting)
- Institut Jean Godinot — Reims, France (Recruiting)
- Centre Henri Becquerel — Rouen, France (Recruiting)
- Institut Curie - Hôpital René Huguenin — Saint-Cloud, France (Recruiting)
- Centre Paul Strauss — Strasbourg, France (Recruiting)
- Institut Claudius Regaud — Toulouse, France (Recruiting)
- Institut de Cancérologie de Lorraine — Vandœuvre-lès-Nancy, France (Recruiting)
- Institut Gustave Roussy — Villejuif, France (Recruiting)
Study contacts
- Study coordinator: Lise Bosquet, MsC
- Email: l-bosquet@unicancer.fr
- Phone: 0033668642660
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.