Non-Squamous Non-Small Cell Lung Cancer
Conditions
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.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* 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
Exclusion criteria
* Participation in a clinical trial evaluating anti-cancer therapies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression-free survival | 18 months |
Secondary
| Measure | Time frame |
|---|---|
| Modality of treatment with Avastin (dose, duration, associated chemotherapy) | 18 months |
| Overall survival | 18 months |
| Clinical (diagnosis, therapies, comorbidity) and demographic characteristics of patients initiated on Avastin treatment | 18 months |
| Quality of Life: Functional Assessment of Cancer Therapy-Lung (FACT-L) questionnaire | 18 months |
| Treatment of non-squamous NSCLC in clinical practice | 18 months |
| Safety: Incidence of adverse events | 18 months |
Countries
France