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This is an observational multicenter study. A cross-sectional descriptive study of patients with locally advanced or metastatic Non Small Cell Lung Cancer with activating EGFR mutation treated by any first line therapy will be used to identify cohort with a prospective follow-up of patients initiating a treatment by osimertinib in first line
This is an observational multicenter study combining a descriptive cross-sectional survey and a prospective cohort design to address the study objectives.
Part A is a prospective study targeting a cohort of patients focusing on patients with locally advanced or metastatic NSCLC with activating EGFR mutation initiating a treatment by osimertinib in first line will be conducted to address the primary objective of this study and remaining secondary objectives.
Part B is an additional descriptive cross-sectional survey of all patients with locally advanced or metastatic NSCLC with activating EGFR mutation treated by any first line therapy will be collected at the study participating sites. The study part which is cross sectional will allow to characterize the population of patients with locally advanced or metastatic NSCLC with activating EGFR mutation treated in first line, the day of first line initiation.
Both studies will be initiated at the same time (depending on osimertinib reimbursement in France - expected on October 2020). Part A will have an enrolment period of approximately 18 months and a follow-up period of 36 months. Part B will have an enrolment period of 12 months.
For Part A, patients must be newly treated in first line and the index date will be the day of first line treatment initiation. Patients will be followed-up for all routine visits recorded until time to second progression. After the relapse of second line therapy, patients will be followed-up every 6 months for overall survival only until 36 months.
For Part B, patients newly diagnosed with locally advanced or metastatic NSCLC who are treatment naive or patients who were diagnosed at an earlier stage but have progressed to metastatic NSCLC during the selection period will be included.
Patients will be followed up from enrolment in part A until death, loss to follow-up, withdrawal of consent or study end date, whichever occurs first.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Osimertinib | Drug | Single arm treated by osimertinib |
|
| Measure | Description | Time Frame |
|---|---|---|
| Overall survival | 36-months overall survival defined as time from index date until death from any cause | 36 months |
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Inclusion Criteria:
Descriptive cross-sectional survey (Population B)
Prospective cohort (Population A)
Exclusion Criteria (Population A):
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Study combining a descriptive cross-sectional survey (part B) and a prospective cohort design (part A).
Patients with locally advanced or metastatic Non Small Cell Lung Cancer (NSCLC) with activating EGFR mutation initiating a treatment by osimertinib in first line (Population A)
Patients with locally advanced or metastatic NSCLC with activating EGFR mutation treated by any first line therapy (population B)
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| Name | Affiliation | Role |
|---|---|---|
| Jean-Bernard Auliac | CHI Creteil, France | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Abbeville | France | ||||
| Research Site |
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| Aix-en-Provence |
| France |
| Research Site | Angers | France |
| Research Site | Antibes | France |
| Research Site | Avignon | France |
| Research Site | Bastia | France |
| Research Site | Bayonne | France |
| Research Site | Bordeaux | France |
| Research Site | Bourg-en-Bresse | France |
| Research Site | Brest | France |
| Research Site | Cannes | France |
| Research Site | Chambéry | France |
| Research Site | Chauny | France |
| Research Site | Cholet | France |
| Research Site | Clermont-Ferrand | France |
| Research Site | Colmar | France |
| Research Site | Contamine-sur-Arve | France |
| Research Site | Créteil | France |
| Research Site | Elbeuf | France |
| Research Site | Epagny METZ Tessy | France |
| Research Site | Évreux | France |
| Research Site | La Roche-sur-Yon | France |
| Research Site | Libourne | France |
| Research Site | Limoges | France |
| Research Site | Lyon | France |
| Research Site | Marseille | France |
| Research Site | Meaux | France |
| Research Site | Mulhouse | France |
| Research Site | Orléans | France |
| Research Site | Paris | France |
| Research Site | Poitiers | France |
| Research Site | Quimper | France |
| Research Site | Reims | France |
| Research Site | Rouen | France |
| Research Site | Saint-Denis | France |
| Research Site | Saint-Grégoire | France |
| Research Site | Saint-Pierre | France |
| Research Site | Saint-Priest-en-Jarez | France |
| Research Site | Saint-Quentin | France |
| Research Site | Toulon | France |
| Research Site | Toulouse | France |
| Research Site | Valenciennes | France |
| Research Site | Vannes | France |
| Research Site | Villefranche-sur-Saône | France |
| Research Site | Villenave-dornon | France |
| Research Site | Villeurbanne | France |
| ID | Term |
|---|---|
| D002289 | Carcinoma, Non-Small-Cell Lung |
| ID | Term |
|---|---|
| D002283 | Carcinoma, Bronchogenic |
| D001984 | Bronchial Neoplasms |
| D008175 | Lung Neoplasms |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| ID | Term |
|---|---|
| C000596361 | osimertinib |
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