| Literature DB >> 20156700 |
Alexandre Bozec1, Patricia Formento, Jean-Louis Fischel, Marie-Christine Etienne-Grimaldi, Gérard Milano.
Abstract
Head-and-neck (H&N) tumor re-growth is clinically observed after arrest of anti-EGFR therapies. In the present study, we compared, for a similar dose exposure to anti-EGFR therapies, constant (CS) with tapered (TS) schedules (i.e. progressive dose reduction) for cetuximab, a mAb, and gefitinib, a TKI. Mice bearing CAL33 H&N tumors with high EGFR content were treated with cetuximab or gefitinib. CS consisted of 7 days of cetuximab or gefitinib administration and TS of 7 days of drugs followed by 7 days of administration at decreased doses (divided by 2 every day). Gefitinib TS but not CS slowed down tumor re-growth. Cetuximab TS had a stronger and longer-lasting effect than CS, paralleled by a down-regulation of EGFR expression. Whatever the drug, TS decreased tumor re-growth more efficiently than CS. This new drug schedule could be of interest in the management of anti-EGFR based therapies in H&N cancer. (c) 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20156700 DOI: 10.1016/j.oraloncology.2009.11.010
Source DB: PubMed Journal: Oral Oncol ISSN: 1368-8375 Impact factor: 5.337