Arena, SabrinaSiravegna, GiuliaMussolin, BenedettaKearns, Jeffrey D.Wolf, Beni B.Misale, SandraLazzari, LucaBertotti, AndreaTrusolino, LivioAdjei, Alex A.Montagut Viladot, ClaraDi Nicolantonio, FedericaNering, RachelBardelli, Alberto2016-04-272016-04-272016Arena S, Siravegna G, Mussolin B, Kearns JD, Wolf BB, Misale S. et al. MM-151 overcomes acquired resistance to cetuximab and panitumumab in colorectal cancers harboring EGFR extracellular domain mutations. Sci Transl Med. 2016 Feb 3;8(324):324ra14. doi: 10.1126/scitranslmed.aad5640.1946-6234http://hdl.handle.net/10230/26180The anti-epidermal growth factor receptor (EGFR) antibodies cetuximab and panitumumab are used to treat RAS wild-type colorectal cancers (CRCs), but their efficacy is limited by the emergence of acquired drug resistance. After EGFR blockade, about 20% of CRCs develop mutations in the EGFR extracellular domain (ECD) that impair antibody binding and are associated with clinical relapse. We hypothesized that EGFR ECD-resistant variants could be targeted by the recently developed oligoclonal antibody MM-151 that binds multiple regions of the EGFR ECD. MM-151 inhibits EGFR signaling and cell growth in preclinical models, including patient-derived cells carrying mutant EGFR. Upon MM-151 treatment, EGFR ECD mutations decline in circulating cell-free tumor DNA (ctDNA) of CRC patients who previously developed resistance to EGFR blockade. These data provide molecular rationale for the clinical use of MM-151 in patients who become resistant to cetuximab or panitumumab as a result of EGFR ECD mutations.application/pdfengThis is tha autor's version of the work. It is postered here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in Science Translational Medicine on 2016 Feb 3;8(324):324ra14. doi: 10.1126/scitranslmed.aad5640.Còlon -- Càncer -- Aspectes genèticsinfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1126/scitranslmed.aad5640info:eu-repo/semantics/openAccess