Carcinoma, Squamous Cell Clinical Trial
Official title:
MULTICENTER, PROSPECTIVE, OBSERVATIONAL OF ERLOTINIB AS SECOND-LINE TREATMENT IN PATIENTS WITH NON-SMALL CELL (NSCLC) LUNG CANCER WITH PREDOMINANTLY SQUAMOUS HISTOLOGY AND CARRIERS OF THE GENE (EGFR) EPIDERMAL GROWTH FACTOR RECEPTOR NATIVE
OBJECTIVE study the effectiveness of the administration of Erlotinib 150 mg/Day v.o. in
second-line treatment in patients with lung cancer advanced non-small of histology
predominantly flaky by assessing the survival free of progression (SLP).
Design Studio postautoritation of multicenter observational follow-up prospective (EPA-SP)
type.
DISEASE OTRASTORNO A study of cell Lung Cancer not small (NSCLC). MEDICATION object data to
study the drug under study is erlotinib.
-Dose and treatment guidelines follow the corresponding product sheet. Management of dosage
and adverse effects specified in point H. 15 of the Protocol.
POPULATION in study and number TOTAL of subjects population under study: adult patients with
diagnosis of NSCLC with predominantly squamous histology total number of subjects: the
participation of approximately 51 patients is expected DISEASE OR DISORDER TO STUDY Non
Small Cell Lung Cancer (NSCLC). MEDICATION DATA OBJECT OF STUDY The drug under study is
erlotinib.
-Dose and treatment guidelines Follow the corresponding product sheet. Management of dosage
and adverse effects specified in point H. 15 of the Protocol.
STUDY POPULATION AND NUMBER TOTAL OF SUBJECTS Study: adult patients with diagnosis of NSCLC
with predominantly squamous histology total number of subjects: the participation of
approximately 51 patients is expected.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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