An Observational Study of Avastin (Bevacizumab) in Combination With Chemotherapy in Patients With Metastatic or Recurrent Non-Squamous Non-Small Cell Lung Cancer
A Cohort Study of First-line Treatment of Patients With Unresectable Advanced (Stage IIIB), Metastatic (Stage IV) or Recurrent Non Squamous Non-small Cell Lung Cancer (NSCLC), Starting a Treatment With Bevacizumab (Avastin®) in Combination With Chemotherapy.
1 other identifier
observational
423
1 country
152
Brief Summary
This observational study will evaluate modality, efficacy and safety of Avastin (bevacizumab) as first-line treatment in combination with chemotherapy in patients with inoperable advanced, metastatic or recurrent non-squamous non-small cell lung cancer in clinical practice. Data will be collected for each patient for 18 months from initiation of Avastin therapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2010
Typical duration for all trials
152 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2010
CompletedFirst Submitted
Initial submission to the registry
April 6, 2011
CompletedFirst Posted
Study publicly available on registry
April 11, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2013
CompletedNovember 2, 2016
November 1, 2016
2.8 years
April 6, 2011
November 1, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
Progression-free survival
18 months
Secondary Outcomes (6)
Clinical (diagnosis, therapies, comorbidity) and demographic characteristics of patients initiated on Avastin treatment
18 months
Modality of treatment with Avastin (dose, duration, associated chemotherapy)
18 months
Overall survival
18 months
Safety: Incidence of adverse events
18 months
Quality of Life: Functional Assessment of Cancer Therapy-Lung (FACT-L) questionnaire
18 months
- +1 more secondary outcomes
Study Arms (1)
Cohort
Eligibility Criteria
Patients With Metastatic or Recurrent Non-Squamous Non-Small Cell Lung Cancer
You may qualify if:
- Adult patients, \>/= 18 years of age
- Inoperable advanced, metastatic or recurrent non-squamous non-small cell lung cancer (NSCLC)
- Treating physician's decision to initiate first-line Avastin treatment
You may not qualify if:
- Participation in a clinical trial evaluating anti-cancer therapies
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (152)
Unknown Facility
Abbeville, 80142, France
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Agen, 47000, France
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Aix-en-Provence, 13616, France
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Aix-en-Provence, 13617, France
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Alès, 30100, France
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Ambilly, 74100, France
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Amiens, 80090, France
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Amilly, 45200, France
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Angers, 49933, France
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Annecy, 74000, France
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Antibes, 06600, France
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Armentières, 59421, France
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Arras, 62022, France
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Aubenas, 07205, France
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Aulnay-sous-Bois, 93602, France
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Auxerre, 89000, France
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Bar-le-Duc, 55012, France
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Bastia, 20200, France
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Bastia, 20604, France
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Bayeux, 14401, France
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Bayonne, 64100, France
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Bayonne, 64109, France
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Besançon, 25030, France
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Beuvry, 62660, France
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Biarritz, 64204, France
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Bobigny, 93009, France
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Bois-Guillaume, 76233, France
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Bordeaux, 33030, France
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Bordeaux, 33077, France
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Boulogne-sur-Mer, 62321, France
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Bourg-en-Bresse, 01012, France
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Brest, 29200, France
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Brest, 29240, France
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Brive-la-Gaillarde, 19312, France
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Bron, 69677, France
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Bry-sur-Marne, 94366, France
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Caen, 14076, France
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Cagnes-sur-Mer, 06805, France
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Cahors, 46005, France
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Carcassonne, 11890, France
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Chalon-sur-Saône, 71100, France
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Chambray-lès-Tours, 37175, France
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Charleville-Mézières, 08011, France
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Chaumont, 52014, France
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Chauny, 02303, France
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Châteauroux, 36019, France
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Cherbourg Octeville, 50102, France
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Clamart, 92141, France
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Clermont-Ferrand, 63003, France
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Colmar, 68024, France
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Compiègne, 60204, France
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Compiègne, 60321, France
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Cornebarrieu, 31700, France
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Creil, 60109, France
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Créteil, 94010, France
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Dax, 40107, France
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Dijon, 21000, France
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Dunkirk, 59240, France
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Eaubonne, 95602, France
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Épernay, 51200, France
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Évreux, 27025, France
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Fontainebleau, 77305, France
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Gap, 05007, France
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Gleizé, 69400, France
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Granville, 50406, France
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Hyères, 83400, France
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La Chaussée-Saint-Victor, 41260, France
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La Roche-sur-Yon, 85925, France
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La Seyne-sur-Mer, 83500, France
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La Source, 45100, France
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Le Mans, 72015, France
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Le Perreux-sur-Marne, 94170, France
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Levallois-Perret, 92309, France
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Libourne, 33505, France
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Liévin, 62806, France
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Lille, 59003, France
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Lille, 59037, France
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Limoges, 87042, France
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Longjumeau, 91161, France
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Lorient, 56322, France
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Lormont, 33310, France
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Lyon, 69275, France
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Lyon, 69317, France
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Lyon, 69338, France
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Lyon, 69373, France
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Lyon, 69424, France
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Mareuil-lès-Meaux, 77100, France
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Marseille, 13274, France
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Maubeuge, 59604, France
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Meaux, 77104, France
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Metz, 57000, France
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Metz-Tessy, 74370, France
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Mont-de-Marsan, 40024, France
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Montauban, 82013, France
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Montélimar, 26216, France
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Montfermeil, 93370, France
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Montpellier, 34967, France
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Mulhouse, 68070, France
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Nancy, 54100, France
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Narbonne, 11108, France
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Nemours, 77796, France
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Neuilly-sur-Seine, 92521, France
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Nevers, 58033, France
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Osny, 95520, France
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Paris, 75015, France
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Paris, 75181, France
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Paris, 75571, France
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Paris, 75674, France
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Paris, 75877, France
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Paris, 75908, France
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Pau, 64046, France
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Perpignan, 66046, France
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Pierre-Bénite, 69495, France
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Pontarlier, 25304, France
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Pontoise, 95300, France
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Rambouillet, 78514, France
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Reims, 51056, France
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Reims, 51057, France
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Reims, 51100, France
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Rennes, 35033, France
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Rouen, 76000, France
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Rouen, 76044, France
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Saint-Aubin-lès-Elbeuf, 76410, France
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Saint-Herblain, 44805, France
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Saint-Jean, 31240, France
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Saint-Lô, 50009, France
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Saint-Priest-en-Jarez, 42271, France
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Saint-Quentin, 02321, France
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Saintes, 17108, France
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Senlis, 60309, France
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Soissons, 02209, France
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Ste Feyre, 23000, France
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Strasbourg, 67000, France
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Strasbourg, 67010, France
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Strasbourg, 67065, France
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Strasbourg, 67085, France
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Strasbourg, 67091, France
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Tarbes, 65000, France
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Thionville, 57126, France
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Thonon-les-Bains, 74203, France
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Toulon, 83041, France
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Toulon, 83056, France
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Toulouse, 31076, France
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Vandœuvre-lès-Nancy, 54511, France
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Vannes, 56001, France
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Vannes, 56017, France
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Verdun, 55107, France
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Versailles, 78004, France
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Vesoul, 70014, France
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Vénissieux, 69200, France
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Vichy, 3201, France
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Villeneuve-Saint-Georges, 94195, France
Study Officials
- STUDY DIRECTOR
Clinical Trials
Hoffmann-La Roche
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 6, 2011
First Posted
April 11, 2011
Study Start
July 1, 2010
Primary Completion
May 1, 2013
Study Completion
May 1, 2013
Last Updated
November 2, 2016
Record last verified: 2016-11