Non-Squamous Non-Small Cell Lung Cancer
Conditions
Brief summary
This prospective, observational study will assess the effectiveness and safety of Avastin (bevacizumab) as 1st line therapy in elderly patients with advanced non-squamous non-small cell lung cancer in clinical practice. Therapy with Avastin and standard chemotherapy will be administered according to the treating physician. Data will be collected for approximately 4 years.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Adult patients, \>= 65 years of age * Diagnosis of advanced non squamous Non-Small Cell Lung Carcinoma (nsNSCLC, stage IIIB or IV) for whom the physician has decided to initiate a treatment with Avastin combined with chemotherapy as 1st line therapy * Having received oral and written information about the study, and having signed a written consent form
Exclusion criteria
* Participation in a cancer clinical trial with an investigational medicinal product other than this study * Patient previously treated with Avastin * Patient under supervision or guardianship
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients treated with a chemotherapy in combination with Avastin including description of chemotherapy regimens and management of Avastin treatment | Approximately 4 years |
Secondary
| Measure | Time frame |
|---|---|
| Characteristics of patients with advanced non-squamous non-small cell lung cancer | Approximately 4 years |
| Tumor characteristics of patients with advanced non-squamous non-small cell lung cancer | Approximately 4 years |
| Progression-free survival | Approximately 4 years |
| Overall survival | Approximately 4 years |
| Quality of Life | Approximately 4 years |
| Safety: Incidence of adverse events | Approximately 4 years |
| Reasons of non-use of Avastin as first-line therapy | Approximately 4 years |
Countries
France