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Predictive factors of response to anti-EGFR treatments in colorectal cancer Volume 95, issue 1, janvier 2008

Authors
Inserm UMR-S775 Bases moléculaires de la réponse aux xénobiotiques, Université Paris-Descartes, 45, rue des Saints-Pères, 75006 Paris, CHU Ambroise-Paré, Service d’hépato-gastroentérologie et oncologie digestive, Boulogne-Billancourt ; Université de Versailles-Saint-Quentin-en-Yvelines, Versailles, Hôpital européen Georges-Pompidou, Service de biochimie, Paris

Among the targeted therapies used in the treatment of metastatic colorectal cancer (CRC), cetuximab was registered in France in 2004. This chimeric antibody inhibiting the Epidermal Growth receptor (EGFR) has been demonstrated to be efficient in the treatment of irinotecan-resistant metastatic CRC expressing the EGFR. Panitumumab, a fully humanized anti-EGFR antibody should soon be registered after failure of conventional chemotherapies. However, these costly and potentially toxic treatments are efficient in a little proportion of patients. It is so necessary to identify some factors able to better define whose patients will benefit from these treatments. The major potential predictive factors of response to cetuximab and/or panitumumab that have been evaluated in the litterature, which are summarized in this review, are molecular factors involved more or less directly in the EGF signaling pathway. Among them, KRAS mutations, EGFR gene copy number and, more recently, epiregulin and amphiregulin expression are those, along with skin toxicity, which appear to be the most relevant and which will have to be evaluated in future clinical trials to be validated before being incorprated in therapeutic strategy of CRC.