Several arguments are in favor of a therapeutic monitoring for the erlotinib, therefore, a pharmacokinetic (PK) has been prepared using data from the literature. This model must be validated at concentrations achieved in practice. This is a preliminary study before the implementation of a randomized trial confirming the therapeutic monitoring of erlotinib through this model.
Study Type
OBSERVATIONAL
Enrollment
50
Plasma dosage of erlotinib and OSI-420 is made from the blood usually taken Further information are collected in the medical record of the patient during the CT scan reassessment after collection.
Service de Pneumologie Nouvel Hôpital Civil
Strasbourg, Alsace, France
RECRUITINGDifference between plasma concentrations of erlotinib concentrations observed and predictive model
Time frame: 1 year
Correlation of Blood levels outsized with severe side effects or compromising the vital prognosis (treatment response, adherence (assessed by the test Morisky Green)
Evaluation of interest to assay the active metabolite OSI-420 Observation between incidence of clinical problems (ineffectiveness, toxicity, adherence) and blood concentrations of erlotinib outsized. Evaluation of the potential clinical benefit to provide a dosage of erlotinib
Time frame: 1 year
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