This observational study will evaluate the efficacy and safety of Tarceva (erlotinib) in second line in patients with locally advanced or metastatic squamous non-small cell lung cancer (NSCLC) after failure of first line platinum-based chemotherapy. Eligible patients will be followed for 12 months.
Study Type
OBSERVATIONAL
Enrollment
152
Progression-free survival
Time frame: 2 years
Clinical/demographic patients characteristics at baseline
Time frame: 2 years
Treatment schedules: Dose/duration/modifications/interruptions
Time frame: 2 years
Overall survival
Time frame: 2 years
Safety: Incidence of adverse events
Time frame: 2 years
Quality of life: FACT-L version 4 questionnaire
Time frame: 2 years
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Abbeville, France
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Agen, France
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Aix-en-Provence, France
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Aix-en-Provence, France
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Amiens, France
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Angers, France
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Antibes, France
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Armentières, France
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Aulnay-sous-Bois, France
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Bar-le-Duc, France
...and 100 more locations