The main objective of this study is to validate the utility of IgE anti-cetuximab in the treatment strategy to identify patients at risk for a severe allergic reaction to cetuximab (grade 3 or 4 of the classification of NCI) and thus reduce the incidence of severe reactions.
Study Type
OBSERVATIONAL
Enrollment
303
The IgE anti cetuximab test will then be conducted by an ELISA test
CHU
Amiens, France
Centre hospitalier
Bayeux, France
CHU
Caen, France
Centre François Baclesse
Caen, France
Validate the utility of an IgE anti-cetuximab test in the treatment strategy
We hypothesize that a positive specific IgE assay predicts the occurrence of an allergic reaction during the first dose of cetuximab. Thus, in population areas where the prevalence of specific IgE positive plasma is higher, the use of alternative therapies in patients with a positive test would reduce the incidence of anaphylactic reactions to cetuximab. If the use of specific IgE anti-cetuximab in the treatment strategy is effective, there will be reduction in the incidence of anaphylaxis to cetuximab in the participating centers.
Time frame: 3 years
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Centre Georges-François Leclerc
Dijon, France
Centre Oscar Lambret
Lille, France
CHRU Lille
Lille, France
CHU Charles Nicolle
Rouen, France
Centre Henri Becquerel
Rouen, France
Centre Paul Strauss
Strasbourg, France