This prospective observational study will evaluate the efficacy and safety of second-line Tarceva (erlotinib) in patients with previously treated advanced non-small cell lung cancer with confirmed wild-type epidermal growth factor receptor (EGFR) gene. The aim of the study is to identify from baseline clinical and demographic patient characteristics prognostic factors related to overall survival with second-line Tarceva treatment. Data will be collected from eligible patients for up to 2 years.
Study Type
OBSERVATIONAL
Enrollment
355
Unnamed facility
Vitoria-Gasteiz, Alava, Spain
Unnamed facility
Elda, Alicante, Spain
Unnamed facility
Mahon, Balearic Islands, Spain
Unnamed facility
Palma de Mallorca, Balearic Islands, Spain
Unnamed facility
Barcelona, Barcelona, Spain
Unnamed facility
Correlation of overall survival with baseline clinical/demographic patient characteristics
Time frame: approximately 2 years
Correlation of overall survival with baseline tumour characteristics
Time frame: approximately 2 years
Correlation of overall survival with previous treatment regimens
Time frame: approximately 2 years
Objective response rate (ORR), tumour assessments according to RECIST criteria
Time frame: approximately 2 years
Disease control rate
Time frame: approximately 2 years
Progression-free survival
Time frame: approximately 2 years
Safety: Incidence of adverse events
Time frame: approximately 2 years
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Barcelona, Barcelona, Spain
Unnamed facility
Barcelona, Barcelona, Spain
Unnamed facility
Barcelona, Barcelona, Spain
Unnamed facility
Cáceres, Caceres, Spain
Unnamed facility
Santander, Cantabria, Spain
...and 31 more locations